JP2001206183A - Air bag cover for vehicle - Google Patents
Air bag cover for vehicleInfo
- Publication number
- JP2001206183A JP2001206183A JP2000324901A JP2000324901A JP2001206183A JP 2001206183 A JP2001206183 A JP 2001206183A JP 2000324901 A JP2000324901 A JP 2000324901A JP 2000324901 A JP2000324901 A JP 2000324901A JP 2001206183 A JP2001206183 A JP 2001206183A
- Authority
- JP
- Japan
- Prior art keywords
- component
- weight
- ethylene
- airbag cover
- olefin
- 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
- 229920001577 copolymer Polymers 0.000 claims abstract description 34
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000005977 Ethylene Substances 0.000 claims abstract description 32
- 229920001971 elastomer Polymers 0.000 claims abstract description 26
- 229920002725 thermoplastic elastomer Polymers 0.000 claims abstract description 23
- 239000004711 α-olefin Substances 0.000 claims abstract description 22
- 239000005060 rubber Substances 0.000 claims abstract description 18
- 239000000155 melt Substances 0.000 claims abstract description 9
- 230000000704 physical effect Effects 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 17
- 229920002554 vinyl polymer Polymers 0.000 claims description 15
- 238000000465 moulding Methods 0.000 claims description 13
- 229920001400 block copolymer Polymers 0.000 claims description 11
- 150000001993 dienes Chemical class 0.000 claims description 9
- 239000000806 elastomer Substances 0.000 claims description 8
- 229920005672 polyolefin resin Polymers 0.000 claims description 8
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
- 238000001746 injection moulding Methods 0.000 abstract description 13
- 229920005989 resin Polymers 0.000 abstract description 8
- 239000011347 resin Substances 0.000 abstract description 8
- 238000005452 bending Methods 0.000 abstract description 4
- 239000002356 single layer Substances 0.000 abstract description 4
- 239000000243 solution Substances 0.000 abstract 1
- -1 ethylene, propylene, 1-butene Chemical class 0.000 description 22
- 229920000642 polymer Polymers 0.000 description 11
- 238000004132 cross linking Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 6
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000011162 core material Substances 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000010097 foam moulding Methods 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920006380 polyphenylene oxide Polymers 0.000 description 2
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- RSGZQYVTVPJMTG-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhex-3-yn-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)C#CC(C)(C)OOC(=O)C1=CC=CC=C1 RSGZQYVTVPJMTG-UHFFFAOYSA-N 0.000 description 1
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- UBRWPVTUQDJKCC-UHFFFAOYSA-N 1,3-bis(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC(C(C)(C)OOC(C)(C)C)=C1 UBRWPVTUQDJKCC-UHFFFAOYSA-N 0.000 description 1
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- ODBCKCWTWALFKM-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhex-3-yne Chemical compound CC(C)(C)OOC(C)(C)C#CC(C)(C)OOC(C)(C)C ODBCKCWTWALFKM-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- ZZLCFHIKESPLTH-UHFFFAOYSA-N 4-Methylbiphenyl Chemical compound C1=CC(C)=CC=C1C1=CC=CC=C1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- PCBPVYHMZBWMAZ-UHFFFAOYSA-N 5-methylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C)CC1C=C2 PCBPVYHMZBWMAZ-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 206010016322 Feeling abnormal Diseases 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- RTACIUYXLGWTAE-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene;styrene Chemical compound C=CC=C.CC(=C)C=C.C=CC1=CC=CC=C1 RTACIUYXLGWTAE-UHFFFAOYSA-N 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
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000012792 core layer Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 229920005680 ethylene-methyl methacrylate copolymer Polymers 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- DZCCLNYLUGNUKQ-UHFFFAOYSA-N n-(4-nitrosophenyl)hydroxylamine Chemical compound ONC1=CC=C(N=O)C=C1 DZCCLNYLUGNUKQ-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003682 vanadium compounds Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Air Bags (AREA)
- Instrument Panels (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、乗物用エアバッグ
カバーに関する。詳しくは、自動車等の高速移動体に設
置され、衝突事故等の際に、その衝撃や変形を感知する
ことにより膨張展開することにより乗員を保護するエア
バッグを収納するカバーに関するものである。The present invention relates to a vehicle airbag cover. More specifically, the present invention relates to a cover that is installed on a high-speed moving body such as an automobile and stores an airbag that protects an occupant by inflating and deploying by sensing the impact or deformation in the event of a collision or the like.
【0002】[0002]
【従来の技術】エアバッグシステムは、自動車等の衝突
の際に運転手や搭乗者を保護するシステムで、衝突の際
の衝撃を感知する装置とエアバッグ装置からなる。エア
バッグ装置は、エアバッグ、エアバッグ作動装置、およ
びそれを収納するカバーからなり、これら装置はステア
リングホイール、助手席前面のインストルメントパネル
内、フロントピラー、サイドピラー、リアピラー、座席
シート側面部等に設置される。そして車両の衝突などに
より大きな衝撃を受けた時には、エアバッグケース内に
収納されているエアバッグが膨張し、エアバッグカバー
を内部から押し開き、該エアバッグを車室内に展開させ
るようになっている。2. Description of the Related Art An airbag system is a system for protecting a driver or a passenger in the event of a collision of an automobile or the like, and comprises a device for sensing a shock in the event of a collision and an airbag device. The airbag device comprises an airbag, an airbag actuating device, and a cover for accommodating the same. These devices include a steering wheel, an instrument panel in front of a passenger seat, a front pillar, a side pillar, a rear pillar, and a side portion of a seat. Installed in When a large impact is received due to a vehicle collision or the like, the airbag housed in the airbag case is inflated, the airbag cover is pushed open from the inside, and the airbag is deployed in the passenger compartment. I have.
【0003】このような構造に用いられるエアバッグカ
バーとしては金属を芯材としてウレタン発泡成形したも
のや、製品重量の軽量化を目的として芯材を変性ポリフ
ェニレンオキサイドと6−ナイロンとのポリマーアロイ
といった硬質プラスチックを用い、6−ナイロンネット
等による補強材をインサートしてウレタン発泡成形した
ものがある。しかし変性ポリフェニレンオキサイドと6
−ナイロンとのポリマーアロイを芯材として用いた場
合、製品重量は軽量化できるが低温時の展開性能が低下
する傾向があり、また、ネット状の補強材をインサート
するため、多数の複雑な製造工程が必要である。[0003] The airbag cover used in such a structure is formed by urethane foam molding using a metal as a core material, or a polymer alloy of modified polyphenylene oxide and 6-nylon for the core material for the purpose of reducing the weight of the product. There is urethane foam molding using a hard plastic and inserting a reinforcing material such as a 6-nylon net. However, modified polyphenylene oxide and 6
-When a polymer alloy with nylon is used as the core material, the weight of the product can be reduced, but the deployment performance at low temperatures tends to be reduced. A process is required.
【0004】これらを解決する試みとして、特開平1−
202550号公報、特開平2−171362号公報、
特開平2−220946号公報、特開平3−18925
2号公報に記載されている様な、ソフト感のある熱可塑
性エラストマーを用いた表皮層と、形状保持性のある硬
い熱可塑性エラストマーを用いたコア層からなり、ま
た、前記のウレタン発泡成形の製造工程を簡略化し、生
産性を向上させた二色射出成形カバーや特開平2−17
1364号公報、特開平4−151348号公報、特開
平4−314648号公報、特開平5−38996号公
報に記載されるような単層射出成形による前記の二色射
出成形カバーの欠点であるコストを低減したものが提案
された。これらの提案により、エアバッグ装置における
エアバッグカバーを通常の射出成形機を用いて成形を行
うことが可能となり、しかも、成形サイクルが短縮され
た。As an attempt to solve these problems, Japanese Patent Laid-Open No.
JP-A-202550, JP-A-2-171362,
JP-A-2-220946, JP-A-3-18925
As described in JP-A No. 2 (1994), it comprises a skin layer using a thermoplastic elastomer having a soft feeling, and a core layer using a hard thermoplastic elastomer having shape retention. A two-color injection-molded cover in which the manufacturing process is simplified and the productivity is improved.
No. 1364, JP-A-4-151348, JP-A-4-314648, and JP-A-5-38996, which are disadvantages of the two-color injection-molded cover by single-layer injection molding. Were proposed. With these proposals, it is possible to form an airbag cover in an airbag apparatus using a normal injection molding machine, and the molding cycle is shortened.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、最新の
乗員保護用エアバッグ装置においては、インストルメン
トパネルの助手席前面の開口部に設置されたり、フロン
トあるいはサイドピラー等に設置されるケースもあり、
この場合隣接する部材と剛性感・外観の差がより少ない
ものが求められる。前記の二色射出成形や単層射出成形
によるエアバッグカバーにおいては、エアバッグ展開時
にエアバッグカバーを容易に開裂させるための薄肉部
(ティアライン)をもつことから、剛性感がわるく、耐
熱変形性において十分満足できるものではなかった。However, in the latest occupant protection airbag devices, there are cases where the airbag device is installed at an opening in the front of a passenger seat of an instrument panel, or installed at a front or side pillar.
In this case, a member having a smaller difference in rigidity and appearance from an adjacent member is required. The airbag cover formed by the two-color injection molding or the single-layer injection molding has a thin portion (tear line) for easily tearing the airbag cover when the airbag is deployed, so the rigidity is deteriorated and the heat-resistant deformation is generated. It was not satisfactory in terms of sex.
【0006】これを解決する方法として特開平11−2
36483号公報に記載されるようなエアバッグカバー
も提案されている。このカバーはカバー本体部と該カバ
ー本体部を固定部材へ固定するための取り付け部と該取
り付け部の近傍に配設したヒンジ部とから構成されてお
り、これらが各部が同一面上となる様に形成されてお
り、剛性感は良好であるもののヒンジ部強度を上げるた
め低流動の樹脂を用いていることから複雑な構造のカバ
ーや長尺構造のカバーを成形するにあたっては成形温度
を上げなければならず成形サイクルが長くなり生産性が
悪く、また製品外観においてもフローマーク等の不具合
が発生しやすいといった問題があった。As a method for solving this problem, Japanese Patent Laid-Open No. 11-2
An airbag cover as described in 36483 is also proposed. This cover is composed of a cover main body, a mounting part for fixing the cover main body to the fixing member, and a hinge part arranged near the mounting part, and these parts are on the same plane. Although it has good rigidity, it uses a low-flow resin to increase the strength of the hinge part, so when molding a cover with a complicated structure or a long structure, the molding temperature must be increased. In addition, there is a problem that the molding cycle is long, productivity is low, and defects such as flow marks are liable to occur in the appearance of the product.
【0007】[0007]
【課題を解決するための手段】本発明者等は、上記課題
を解決するため鋭意研究を重ねた結果、特定成分を特定
割合で配合した特定の物性をもつ熱可塑性エラストマー
を用いた乗物用エアバッグカバーが6−ナイロンネット
等をインサートして補強する必要がなく、剛性感および
耐熱変形性に優れる一方、ヒンジ強度や取り付け強度が
高く、該エアバッグの収納用カバーがインストルメント
パネルや自動車の車体そのものに係り止めや直接あるい
は金属インサート等の部品を介し取り付けることがで
き、また成形加工性、製品外観にすぐれ、しかもエアバ
ッグ膨張時に破壊・飛散することなく展開するという安
全性の高いことを見出し本発明を完成するに至ったもの
である。Means for Solving the Problems The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems, and as a result, have found that a vehicle air using a thermoplastic elastomer having specific physical properties in which specific components are blended in a specific ratio. The bag cover does not need to be reinforced by inserting a 6-nylon net or the like, and while being excellent in rigidity and heat-resistant deformation, it has high hinge strength and mounting strength, and the cover for storing the airbag is made of an instrument panel or an automobile. It can be attached to the car body itself or via parts such as metal inserts or metal inserts.It has excellent moldability and product appearance, and it has high safety that it deploys without breaking or scattering when the airbag inflates. The present invention has been completed.
【0008】即ち、本発明の要旨は、下記成分(A)、
(B)の合計が100重量%となるように配合され、且
つ、メルトフローレート(JIS K6758、230
℃、21.17N荷重)が5g/10分以上、曲げ弾性
率(JIS K7203)が550MPa以上800M
Pa未満の物性を有する熱可塑性エラストマーを成形し
てなる乗物用エアバッグカバー。 成分(A):オレフィン系樹脂55〜80重量% 成分(B):エチレンと炭素原子数が6以上のα−オレ
フィンとの共重合体ゴム20〜45重量%、に存在す
る。That is, the gist of the present invention is to provide the following component (A):
(B) is added so as to be 100% by weight, and a melt flow rate (JIS K6758, 230
C., 21.17 N load) is 5 g / 10 min or more, and the flexural modulus (JIS K7203) is 550 MPa or more and 800 M.
A vehicle airbag cover formed by molding a thermoplastic elastomer having physical properties of less than Pa. Component (A): 55 to 80% by weight of olefin resin Component (B): 20 to 45% by weight of a copolymer rubber of ethylene and an α-olefin having 6 or more carbon atoms.
【0009】更に、熱可塑性エラストマーの引張破壊強
さと曲げ弾性率の比が0.03〜0.07である、上記
に記載の乗物用エアバッグカバー、熱可塑性エラストマ
ーのアイゾット衝撃強さが25KJ/m2以上である、
上記に記載の乗物用エアバッグカバー。熱可塑性エラス
トマーのアイゾット衝撃強さが30KJ/m2以上であ
る、上記に記載の乗物用エアバッグカバー、及び、熱可
塑性エラストマーの組成が、 成分(A):オレフィン系樹脂55〜75重量%、及び 成分(B):エチレンと炭素原子数が6以上のα−オレ
フィンとの共重合体ゴム25〜45重量%、である、上
記に記載の乗物用エアバッグカバー、も本発明の態様の
一つである。Further, the vehicle airbag cover described above, wherein the thermoplastic elastomer has a tensile breaking strength to flexural modulus ratio of 0.03 to 0.07, and the thermoplastic elastomer has an Izod impact strength of 25 KJ /. m 2 or more,
A vehicle airbag cover as described above. The vehicle airbag cover described above, wherein the Izod impact strength of the thermoplastic elastomer is 30 KJ / m 2 or more, and the composition of the thermoplastic elastomer is as follows: Component (A): 55 to 75% by weight of an olefin-based resin; And the component (B): 25 to 45% by weight of a copolymer rubber of ethylene and an α-olefin having 6 or more carbon atoms, wherein the airbag cover for a vehicle according to the above is one aspect of the present invention. One.
【0010】更に、成分(A)および成分(B)がそれ
ぞれ下記物性を満足する、上記に記載の乗物用エアバッ
グカバー。 成分(A):メルトフローレートが10〜100g/1
0分、エチレン含量が10%以下であり、重量平均分子
量(Mw)と数平均分子量(Mn)の比が5〜10であ
る、プロピレン・エチレンブロック共重合体、 成分(B):メルトフローレートが10g/10分以
下、密度が0.88g/cm3以下である、エチレンと
炭素原子数が6以上のα−オレフィンとの共重合体、も
本発明の態様の1つである。[0010] Further, the vehicle airbag cover described above, wherein the component (A) and the component (B) each satisfy the following physical properties. Component (A): melt flow rate is 10 to 100 g / 1.
0 minute, a propylene / ethylene block copolymer having an ethylene content of 10% or less and a ratio of weight average molecular weight (Mw) to number average molecular weight (Mn) of 5 to 10, Component (B): melt flow rate Which is 10 g / 10 min or less and has a density of 0.88 g / cm 3 or less, is also an embodiment of the present invention.
【0011】更に加えて、成分(A)および成分(B)
の合計100重量部に対し、下記成分(C)を更に含む
上記に記載の乗物用エアバッグカバー、 成分(C):密度が0.87g/cm3以下のエチレン
と炭素原子数が4以下のα−オレフィンとの共重合体1
〜20重量部、成分(A)および成分(B)の合計10
0重量部に対し、下記成分(D)を更に含む上記に記載
の乗物用エアバッグカバー、 成分(D):スチレン系エラストマー1〜20重量部、
この際の成分(D)のスチレン系エラストマーが芳香族
ビニル−共役ジエンブロック共重合体ゴムの水素添加物
である、上記に記載の乗物用エアバッグカバー、並び
に、自動車のフロントピラー、サイドピラー、及びリア
ピラーのいずれかに設置される、上記に記載の乗物用エ
アバッグカバー。等も本発明の態様の1つである。[0011] In addition, component (A) and component (B)
100 parts by weight of the total of a vehicle air bag cover according to the above further comprising the following components (C), the component (C): density of 0.87 g / cm 3 or less of ethylene and carbon atoms of 4 or less Copolymer with α-olefin 1
-20 parts by weight, the total of the components (A) and (B) being 10
The vehicle airbag cover according to the above, further comprising the following component (D) based on 0 part by weight, Component (D): 1 to 20 parts by weight of a styrene-based elastomer,
The vehicle airbag cover described above, wherein the styrene elastomer of the component (D) is a hydrogenated aromatic vinyl-conjugated diene block copolymer rubber, and a front pillar, a side pillar of an automobile, And the vehicle airbag cover according to the above, which is installed on one of the rear pillar and the rear pillar. And the like are also one embodiment of the present invention.
【発明の実施の形態】[乗物用エアバッグカバー用組成
物] (1)構成材料 本発明のエアバッグカバー用熱可塑性用エラストマー組
成物を構成する材料としては、下記に示す成分(A)及
び(B)の各特定成分を用いる。BEST MODE FOR CARRYING OUT THE INVENTION [Composition for Vehicle Airbag Cover] (1) Constituent Materials The materials constituting the thermoplastic elastomer composition for an airbag cover of the present invention include the components (A) and Each specific component of (B) is used.
【0012】成分(A):オレフィン系樹脂 本発明において用いられるオレフィン系樹脂としては、
例えば、エチレン、プロピレン、1−ブテン等の炭素数
2〜8程度のα−オレフィンの単独重合体、それらのα
−オレフィンとエチレン、プロピレン、1−ブテン、3
−メチル−1−ブテン、1−ペンテン、4−メチル−1
−ペンテン、1−ヘキセン、1−オクテン、1−デセン
等の炭素数2〜20程度の他のα−オレフィンや酢酸ビ
ニル、アクリル酸、メタクリル酸、アクリル酸エステ
ル、メタクリル酸エステル、スチレン、塩化ビニル等の
ビニル化合物との共重合体等が挙げられ、具体的には、
例えば、低・中・高密度ポリエチレン等のエチレン単独
重合体、エチレン−プロピレン共重合体、エチレン−1
−ブテン共重合体、エチレン−4−メチル−1−ペンテ
ン共重合体、エチレン−1−ヘキセン共重合体、エチレ
ン−1−オクテン共重合体、エチレン−酢酸ビニル共重
合体、エチレン−アクリル酸共重合体、エチレン−メタ
クリル酸共重合体、エチレン−メタアクリル酸メチル共
重合体、エチレン−アクリル酸エチル共重合体等のエチ
レン系樹脂、プロピレン単独共重合体、プロピレン−エ
チレン共重合体、プロピレン−エチレン−1−ブテン−
共重合体等のプロピレン系樹脂、及び1−ブテン単独重
合体、1−ブテンエチレン共重合体、1−ブテン−プロ
ピレン共重合体等の1−ブテン系樹脂が挙げられる。Component (A): Olefin resin The olefin resin used in the present invention includes:
For example, homopolymers of α-olefins having about 2 to 8 carbon atoms such as ethylene, propylene, 1-butene, etc .;
-Olefins and ethylene, propylene, 1-butene, 3
-Methyl-1-butene, 1-pentene, 4-methyl-1
-About 2 to 20 carbon atoms such as pentene, 1-hexene, 1-octene, 1-decene and other α-olefins, vinyl acetate, acrylic acid, methacrylic acid, acrylates, methacrylates, styrene, vinyl chloride And the like with a vinyl compound such as, specifically,
For example, ethylene homopolymer such as low / medium / high density polyethylene, ethylene-propylene copolymer, ethylene-1
-Butene copolymer, ethylene-4-methyl-1-pentene copolymer, ethylene-1-hexene copolymer, ethylene-1-octene copolymer, ethylene-vinyl acetate copolymer, ethylene-acrylic acid copolymer Polymers, ethylene resins such as ethylene-methacrylic acid copolymer, ethylene-methyl methacrylate copolymer, ethylene-ethyl acrylate copolymer, propylene homopolymer, propylene-ethylene copolymer, propylene- Ethylene-1-butene-
Examples thereof include propylene-based resins such as copolymers, and 1-butene-based resins such as 1-butene homopolymer, 1-buteneethylene copolymer, and 1-butene-propylene copolymer.
【0013】本発明において用いられるオレフィン系樹
脂としては、以上の中で、プロピレン系樹脂が好まし
く、特にプロピレン・エチレンブロック共重合体が好ま
しい。その場合、エチレン含量が1〜10%、さらに好
ましくは2〜8%のものが好ましい。また、メルトフロ
ーレートは10〜100g/10分(JIS K675
8、230℃、21.17N荷重)、好ましくは15〜
80g/10分であるものが好ましい。さらに重量平均
分子量(Mw)と数平均分子量(Mn)の比が5〜10
であるものが好ましい。As the olefin resin used in the present invention, a propylene resin is preferable, and a propylene / ethylene block copolymer is particularly preferable. In that case, the ethylene content is preferably 1 to 10%, more preferably 2 to 8%. The melt flow rate is 10 to 100 g / 10 min (JIS K675).
8, 230 ° C., 21.17 N load), preferably 15 to
Those having a weight of 80 g / 10 minutes are preferred. Further, the ratio of the weight average molecular weight (Mw) to the number average molecular weight (Mn) is 5 to 10
Is preferred.
【0014】エチレン含量が上記範囲以上のものを用い
た場合、曲げ弾性率、耐熱変形性が低下する傾向にあ
る。又、メルトフローレートが10g/10分未満のも
のを用いた場合、成形加工性、製品外観に劣る傾向にあ
り、100g/10分を越えるものを用いた場合、引張
破壊強さ(JIS K7113、2号ダンベル)やアイ
ゾット衝撃強さ(JIS K7110、−30℃)が低
下する傾向となる。重量平均分子量(Mw)と数平均分
子量(Mn)の比が5未満のものは射出成形時フローマ
ークが発生しやすい傾向にあり、10を越えると曲げ弾
性率、引張破壊強さが低下する傾向となる。When the ethylene content is higher than the above range, the flexural modulus and the heat deformation resistance tend to decrease. When the melt flow rate is less than 10 g / 10 min, the moldability and product appearance tend to be inferior. When the melt flow rate exceeds 100 g / 10 min, the tensile fracture strength (JIS K7113, No. 2 dumbbell) and Izod impact strength (JIS K7110, −30 ° C.) tend to decrease. When the ratio between the weight average molecular weight (Mw) and the number average molecular weight (Mn) is less than 5, flow marks tend to be easily generated during injection molding, and when it exceeds 10, the flexural modulus and tensile strength tend to decrease. Becomes
【0015】成分(B):エチレンと炭素原子数が6以
上のα−オレフィンとの共重合体ゴム 本発明に用いられるエチレンと炭素原子数が6以上のα
−オレフィンとの共重合体ゴムとしては、エチレンと炭
素原子数6〜12のα−オレフィンを水素の共存下に可
溶性バナジウム化合物と有機アルミニウム化合物とから
形成される触媒、又はカミンスキー型触媒等を用いて連
続的に共重合させたものが好適である。該エチレンと炭
素原子数が6以上のα−オレフィンとの共重合体ゴムの
α−オレフィンとしては例えば1−ヘキセン、4−メチ
ル−1−ペンテン、1−オクテン、1−デセンなどが挙
げられ、中でも、1−ヘキセンと1−オクテンが好まし
い。Component (B): Copolymer rubber of ethylene and α-olefin having 6 or more carbon atoms. Ethylene and α having 6 or more carbon atoms used in the present invention.
-As a copolymer rubber with olefin, a catalyst formed from a soluble vanadium compound and an organoaluminum compound in the presence of hydrogen and ethylene and an α-olefin having 6 to 12 carbon atoms, or a Kaminski type catalyst or the like. Those which are used and are continuously copolymerized are preferred. Examples of the α-olefin of the copolymer rubber of ethylene and an α-olefin having 6 or more carbon atoms include 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, and the like. Among them, 1-hexene and 1-octene are preferred.
【0016】該エチレンと炭素原子数6以上のα−オレ
フィンとの共重合体ゴムは、メルトフローレート(JI
S K6758、230℃、21.17N荷重)が10
g/10分以下、さらに好ましくは5g/10分以下で
あるものが好ましい。また、密度(JIS K711
2)は0.88g/cm3以下、さらに好ましくは0.
875g/cm3以下であるものが好ましい。The copolymer rubber of ethylene and an α-olefin having 6 or more carbon atoms has a melt flow rate (JI
SK6758, 230 ° C, 21.17N load) is 10
g / 10 minutes or less, more preferably 5 g / 10 minutes or less. In addition, the density (JIS K711
2) is 0.88 g / cm 3 or less, more preferably 0.1 g / cm 3 or less.
It is preferably 875 g / cm 3 or less.
【0017】メルトフローレートが上記範囲を越えるも
のを用いた場合、成分(A)と成分(B)との配合物の
引張破壊強さ(JIS K7113、2号ダンベル)が
低下する傾向となりエアバッグ作動時のエアバッグカバ
ー展開性能上、問題となる場合がある。又、密度が上記
範囲を越えるものを用いた場合、成分(A)と成分
(B)との配合物のアイゾット衝撃強さ(JIS K7
110、−30℃)が低下する傾向となる。If the melt flow rate exceeds the above range, the tensile strength (JIS K7113, No. 2 dumbbell) of the blend of the component (A) and the component (B) tends to decrease, and the air bag This may cause a problem in airbag cover deployment performance during operation. When the one having a density exceeding the above range is used, the Izod impact strength (JIS K7) of the blend of component (A) and component (B) is used.
110, -30 ° C).
【0018】(2)付加的成分 本発明のエアバッグ収納用カバーの構成材料には、目的
に応じて下記成分を配合することができる。 成分(C):エチレンと炭素原子数が4以下のα−オレ
フィンとの共重合体 熱可塑性エラストマーの低温アイゾット衝撃性能、曲げ
弾性率を調整する目的で配合する。成分(C)のエチレ
ンと炭素原子数が4以下のα−オレフィンとの共重合体
としてはエチレンと炭素原子数が4以下のα−オレフィ
ンとの共重合体のゴム、エチレンと炭素原子数が4以下
のα−オレフィンと非共役ジエンとの共重合体を挙げる
ことができる。(2) Additional Components The following components can be added to the constituent material of the cover for storing an airbag of the present invention according to the purpose. Component (C): Copolymer of ethylene and α-olefin having 4 or less carbon atoms The compound is blended for the purpose of adjusting the low-temperature Izod impact performance and flexural modulus of the thermoplastic elastomer. As the copolymer of ethylene and the α-olefin having 4 or less carbon atoms as the component (C), a rubber of a copolymer of ethylene and an α-olefin having 4 or less carbon atoms, a rubber having ethylene and a carbon atom having 4 or less carbon atoms. Copolymers of 4 or less α-olefins and non-conjugated dienes can be exemplified.
【0019】成分(C)のα−オレフィンとしてはプロ
ピレン、1−ブテンが挙げられる。またエチレンと炭素
原子数が4以下のα−オレフィンと非共役ジエンとの共
重合体の共役ジエン成分としては5−エチリデンノルボ
ルネン、5−メチルノルボルネン、5−ビニルノルボル
ネン、ジシクロペンタジエン等が挙げられる。具体的に
はエチレン・プロピレン共重合体、エチレン・ブテン共
重合体、エチレン・プロピレン・非共役ジエン共重合体
が挙げられる。該エチレンと炭素原子数が4以下のα−
オレフィンとの共重合体は、密度(JIS K711
2)が0.87g/cm3以下であるものが好ましい。
密度が上記範囲を越えたものを用いた場合、低温アイゾ
ッド衝撃性能向上効果が低くなる傾向がある。The α-olefin of the component (C) includes propylene and 1-butene. Examples of the conjugated diene component of the copolymer of ethylene, an α-olefin having 4 or less carbon atoms and a non-conjugated diene include 5-ethylidene norbornene, 5-methylnorbornene, 5-vinylnorbornene, and dicyclopentadiene. . Specific examples include an ethylene / propylene copolymer, an ethylene / butene copolymer, and an ethylene / propylene / non-conjugated diene copolymer. The ethylene and α- having 4 or less carbon atoms
The copolymer with an olefin has a density (JIS K711).
It is preferable that 2) is 0.87 g / cm 3 or less.
If the density exceeds the above range, the effect of improving the low-temperature Izod impact performance tends to decrease.
【0020】成分(D):スチレン系エラストマー 熱可塑性エラストマーの低温アイゾット衝撃強さ、引張
破壊強さ、また製品表面の傷つき性を調整する目的で配
合する。スチレン系エラストマーとしては芳香族ビニル
化合物と共役ジエン化合物の共重合体やエチレンと芳香
族ビニル化合物の共重合体等が挙げられる。なかでも、
少なくとも2個の芳香族ビニル化合物からなる重合体
ブロックと少なくとも1個の共役ジエン化合物からなる
重合体ブロックとからなる芳香族ビニル−共役ジエンブ
ロック共重合体ゴムの水素添加物、少なくとも1個の
芳香族ビニル化合物からなる重合体ブロックと少なくと
も1個の共役ジエン化合物からなる重合体ブロックもし
くは芳香族ビニル化合物−共役ジエン化合物ランダム共
重合体ブロックからなるブロック共重合体ゴムの水素添
加物、及び少なくとも1個の芳香族ビニル化合物から
なる重合体ブロックと芳香族ビニル化合物−共役ジエン
化合物ランダム共重合体ブロックと芳香族ビニル化合物
が漸増する芳香族ビニル化合物−共役ジエン化合物テー
パー共重合体ブロックからなるブロック共重合体ゴムの
水素添加物、が好ましく、なかでも少なくとも2個の芳
香族ビニル化合物からなる重合体ブロックと少なくとも
1個の共役ジエン化合物からなる重合体ブロックとから
なる芳香族ビニル−共役ジエンブロック共重合体ゴムの
水素添加物が特に好ましい。Component (D): Styrene-based elastomer The styrene-based elastomer is blended for the purpose of adjusting the low-temperature Izod impact strength, tensile breaking strength, and scratch resistance of the product surface. Examples of the styrene-based elastomer include a copolymer of an aromatic vinyl compound and a conjugated diene compound and a copolymer of ethylene and an aromatic vinyl compound. Above all,
Hydrogenated aromatic vinyl-conjugated diene block copolymer rubber composed of at least two polymer blocks composed of an aromatic vinyl compound and at least one polymer block composed of a conjugated diene compound, at least one aromatic compound A hydrogenated product of a polymer block composed of an aromatic vinyl compound and a polymer block composed of at least one conjugated diene compound or a block copolymer rubber composed of an aromatic vinyl compound-conjugated diene compound random copolymer block, and at least one Block copolymer consisting of a polymer block composed of two aromatic vinyl compounds, an aromatic vinyl compound-conjugated diene compound random copolymer block, and an aromatic vinyl compound-conjugated diene compound tapered copolymer block in which the aromatic vinyl compound is gradually increased. Hydrogenated polymer rubber, preferably Of these at least two aromatic vinyl composed of an aromatic polymer block comprising a vinyl compound and at least one polymer block comprising a conjugated diene compound - hydrogenated product of conjugated diene block copolymer rubber are particularly preferred.
【0021】芳香族ビニル−共役ジエンブロック共重合
体の水素添加物は、スチレンブロック部が20〜40重
量%、特に25〜35重量%であるものが好ましい。共
役ジエンとしてはブタジエン、イソプレンまたはこれら
の混合物よりなるものが挙げられ、具体的にはスチレン
・ブタジエンブロック共重合体(以下、単にS−B−
S)、スチレン・イソプレンブロック共重合体(以下、
単にS−I−S)、スチレン・ブタジエン・イソプレン
ブロック共重合体(以下、単にS−BI−S)、スチレ
ン・ブタジエン共重合体の水素添加物(以下、単に水添
S−B−S)であるスチレン・エチレン・ブタジエン・
スチレン共重合体(SEBS)等が挙げられる。The hydrogenated aromatic vinyl-conjugated diene block copolymer preferably has a styrene block content of 20 to 40% by weight, particularly 25 to 35% by weight. Examples of the conjugated diene include those composed of butadiene, isoprene or a mixture thereof. Specifically, a styrene-butadiene block copolymer (hereinafter simply referred to as SB-
S), styrene-isoprene block copolymer (hereinafter, referred to as
Simply SIS), styrene-butadiene-isoprene block copolymer (hereinafter simply S-BI-S), hydrogenated styrene-butadiene copolymer (hereinafter simply hydrogenated SBS) Styrene, ethylene, butadiene,
Styrene copolymer (SEBS) and the like.
【0022】(3)その他の任意成分 上記の付加的成分以外に加えて本発明の効果を著しく損
なわない範囲内で、各種目的に応じて配合することがで
きる任意の成分としては着色剤、酸化防止剤、熱安定
剤、光安定剤、紫外線吸収剤、各種無機フィラー、前記
以外の各種熱可塑性エラストマー、中和剤、滑剤、防曇
剤、アンチブロッキング剤、スリップ剤、難燃剤、分散
剤、帯電防止剤、導電性付与剤、金属不活性剤、分子量
調整剤、防菌剤、蛍光増白剤等の各種添加物を挙げるこ
とができる。特に無機フィラーを添加することが望まし
く、タルクがその形状(鱗片形状)から望ましい。使用
量としては樹脂100重量部に対し、3〜15重量部程
度であり、タルク粒径としては平均粒径が1〜6μのも
のが衝撃性能の点から好ましい。(3) Other optional components In addition to the above-mentioned additional components, optional components that can be blended according to various purposes within a range that does not significantly impair the effects of the present invention include colorants, oxidants, and the like. Inhibitors, heat stabilizers, light stabilizers, ultraviolet absorbers, various inorganic fillers, various thermoplastic elastomers other than those described above, neutralizing agents, lubricants, antifogging agents, antiblocking agents, slip agents, flame retardants, dispersants, Examples of the additive include various additives such as an antistatic agent, a conductivity imparting agent, a metal deactivator, a molecular weight regulator, a bactericide, and a fluorescent whitening agent. In particular, it is desirable to add an inorganic filler, and talc is desirable because of its shape (scale shape). The used amount is about 3 to 15 parts by weight with respect to 100 parts by weight of the resin, and the talc particle size is preferably 1 to 6 μm in terms of impact performance.
【0023】(4)配合割合 本発明のエアバッグ収納カバー用熱可塑性エラストマー
組成物を構成する各成分の配合割合は、成分(A)のオ
レフィン系樹脂が55〜80重量%、好ましくは55〜
75重量%であり、成分(B)のエチレンと炭素原子数
が6以上のα−オレフィンとの共重合体がゴムが20〜
45重量%、好ましくは25〜45重量%であり、各成
分の配合比が上記の範囲外においては下記の問題が生じ
る。(4) Blending Ratio The blending ratio of each component constituting the thermoplastic elastomer composition for an airbag storage cover of the present invention is such that the olefin resin of the component (A) is 55 to 80% by weight, preferably 55 to 80% by weight.
75% by weight, and the copolymer of ethylene of component (B) and an α-olefin having 6 or more carbon atoms has a rubber content of 20 to
The content is 45% by weight, preferably 25 to 45% by weight. When the mixing ratio of each component is out of the above range, the following problems occur.
【0024】成分(A)の配合比が55重量%未満のも
のは剛性感、耐熱変形性に劣り、また80重量%を越え
るものは−35℃において30分以上冷却槽にて冷却
後、2分以内に取り付け作業を実施し、展開試験を実施
した際の展開性能に劣るものである。成分(B)の配合
比が20重量%未満のものは低温展開性能に劣り、また
45重量%を越えるものは剛性、耐熱変形性に劣るもの
である。If the compounding ratio of the component (A) is less than 55% by weight, rigidity and heat deformation resistance are inferior. If it exceeds 80% by weight, after cooling in a cooling bath at -35 ° C for 30 minutes or more, It is inferior in deployment performance when mounting work is performed within minutes and a deployment test is performed. If the blending ratio of the component (B) is less than 20% by weight, the low-temperature development performance is inferior, and if it exceeds 45% by weight, the rigidity and the heat deformation resistance are inferior.
【0025】また付加的成分である成分(C)又は/お
よび成分(D)の配合割合は、成分(A)及び(B)の
合計100重量部に対しそれぞれ、1〜20重量部、好
ましくは3〜18重量部である。The proportion of the additional component (C) and / or component (D) is 1 to 20 parts by weight, preferably 100 parts by weight, per 100 parts by weight of the total of components (A) and (B). It is 3 to 18 parts by weight.
【0026】成分(C)の配合比が20重量部を越える
ものは剛性、耐熱変形性に劣り、また引張破壊強さが低
くなる傾向にあり、高温時の展開性能に劣る。成分
(D)の配合比が20重量部を越えるものは剛性、耐熱
変形性に劣り、また成形性に劣り製品外観が低下する傾
向にある。If the compounding ratio of the component (C) exceeds 20 parts by weight, the rigidity and heat deformation resistance are poor, and the tensile strength at break tends to be low. If the compounding ratio of the component (D) exceeds 20 parts by weight, rigidity and heat deformation resistance are inferior, and moldability is inferior and product appearance tends to deteriorate.
【0027】(5)熱可塑性エラストマー組成物の製造 熱可塑性エラストマー組成物は、上記構成成分をヘンシ
ェルミキサー、リボンブレンダー、V型ブレンダー、ス
クリューブレンダー等により均一に混合した後、通常の
押出機やバンバリーミキサー、ロール、ブラベンダー、
ニーダー等を用いて常法で混練して製造されるが、押出
機、特に二軸押出機を用いて製造することが好ましい。
なおその際に、下記の架橋剤や架橋補助剤を配合し動的
に熱処理して部分的に架橋させたものであっても良い。
架橋度としては10〜40%程度とするのが良い。架橋
度は100gのサンプルを144℃のキシレンに浸漬
し、20時間抽出した残さ(残り滓)の元のサンプル重
量に対する割合で表す。(5) Production of Thermoplastic Elastomer Composition The thermoplastic elastomer composition is prepared by uniformly mixing the above components with a Henschel mixer, a ribbon blender, a V-type blender, a screw blender, or the like, and then using a conventional extruder or Banbury. Mixer, roll, brabender,
It is produced by kneading in a conventional manner using a kneader or the like, but is preferably produced using an extruder, particularly a twin-screw extruder.
At that time, the following crosslinking agent or crosslinking auxiliary agent may be blended and dynamically heat-treated to partially crosslink.
The degree of crosslinking is preferably about 10 to 40%. The degree of crosslinking is expressed by the ratio of the residue (residual residue) extracted by immersing a 100 g sample in xylene at 144 ° C. for 20 hours with respect to the original sample weight.
【0028】架橋剤:上記部分的に架橋させるための架
橋剤としては、有機過酸化物を用いることが好ましく、
2,5−ジメチル−2,5−ジ(t−ブチルパーオキ
シ)ヘキサン、2,5−ジメチル−2,5−ジ(t−ブ
チルパーオキシ)−3−ヘキシン、1,3−ビス(t−
ブチルパーオキシイソプロピル)ベンゼン、1,1−ジ
(t−ブチルパーオキシ)−3,5,5−トリメチルシ
クロヘキサン、2,5−ジメチル−2,5−ジ(ベンゾ
イルパーオキシ)−3−ヘキシン、ジミクルパーオキサ
イド等を挙げることができる。添加量は0.01〜1重
量部程度である。Crosslinking agent: As the crosslinking agent for partially crosslinking, it is preferable to use an organic peroxide.
2,5-dimethyl-2,5-di (t-butylperoxy) hexane, 2,5-dimethyl-2,5-di (t-butylperoxy) -3-hexyne, 1,3-bis (t −
Butylperoxyisopropyl) benzene, 1,1-di (t-butylperoxy) -3,5,5-trimethylcyclohexane, 2,5-dimethyl-2,5-di (benzoylperoxy) -3-hexyne, Dimicle peroxide and the like can be mentioned. The amount of addition is about 0.01 to 1 part by weight.
【0029】架橋助剤:上記有機過酸化物により部分的
架橋させる際に用いられる架橋助剤としては、N,N′
−m−フェニレンビスマレイミド、トルイレンビスマレ
イミド、P−キノンジオキシム、ニトロベンゼン、ジフ
ェニルグアニジン、トリメチロールプロパン、ジビニル
ベンゼン、エチレングリコールジメタクリレート、ポリ
エチレングリコールメタクリレート、トリメチロールプ
ロパントリメタクリレート、アリルメタクリレート等の
官能性化合物等を挙げることができる。添加量は0.0
1〜1重量部程度である。Crosslinking aid: N, N 'is used as a crosslinking aid used for partial crosslinking with the above organic peroxide.
-Functionalities such as m-phenylene bismaleimide, toluylene bismaleimide, P-quinone dioxime, nitrobenzene, diphenylguanidine, trimethylolpropane, divinylbenzene, ethylene glycol dimethacrylate, polyethylene glycol methacrylate, trimethylolpropane trimethacrylate, allyl methacrylate, etc. Compounds and the like. The addition amount is 0.0
It is about 1 to 1 part by weight.
【0030】(6)熱可塑性エラストマー組成物の物性 上記乗物用エアバッグカバーの原材料として用いられる
熱可塑性エラストマー組成物の物性は、JIS K67
58による230℃、21.17N荷重におけるメルト
フローレートが5g/10分以上、JIS K7203
による曲げ弾性率が550MPa以上800MPa未
満、である。さらに引張破壊強さ(JISK7113、
2号ダンベル)と曲げ弾性率の比が0.03〜0.0
7、JISK7110による−30℃アイゾット衝撃強
さが25KJ/m2以上、より好ましくは30KJ/m2
以上の物性を有するものが好ましい。(6) Physical Properties of Thermoplastic Elastomer Composition The physical properties of the thermoplastic elastomer composition used as a raw material of the above-mentioned vehicle airbag cover are as specified in JIS K67.
Melt flow rate at 230 ° C. and a load of 21.17 N according to No. 58 is 5 g / 10 min or more, JIS K7203
Is 550 MPa or more and less than 800 MPa. Furthermore, the tensile fracture strength (JISK7113,
No. 2 dumbbell) and the flexural modulus of 0.03-0.0
7. The -30 ° C Izod impact strength according to JIS K7110 is 25 KJ / m 2 or more, more preferably 30 KJ / m 2.
Those having the above physical properties are preferable.
【0031】上記メルトフローレートが上記範囲未満の
ものを用いた場合、生産性に劣り、またフローマークや
ショートショット等の製品不具合が発生しやすい傾向と
なり製品外観が劣る。上記曲げ弾性率が上記範囲未満の
ものを用いた場合、剛性感、耐熱変形性に劣り、上記範
囲を越えたものを用いた場合、アイゾッド衝撃強さが低
下する傾向にある。When the melt flow rate is less than the above range, the productivity is poor, and a product defect such as a flow mark or a short shot tends to occur, resulting in a poor product appearance. If the flexural modulus is less than the above range, the rigidity and heat deformation resistance are inferior. If the flexural modulus exceeds the above range, the Izod impact strength tends to decrease.
【0032】さらに引張破壊強さと曲げ弾性率の比が上
記範囲未満の場合、展開時の変形にともなうヒンジ部や
取り付け部への応力集中に対し強度が低下するので、割
れ、破損等がおこり易く展開性能が低下する傾向があ
る。他方上記範囲を越える場合、引張破壊伸びが低下す
る傾向にあり、展開時、ヒンジ部や取り付け部へ応力集
中が緩和されにくくなり、割れ、破損等がおこり易くな
り展開性能が低下する傾向がある。また、上記アイゾッ
ド衝撃強さが、上記範囲未満のものを用いた場合には低
温展開試験時、取り付け部やヒンジ構造となる部分など
応力集中がおこりやすい部分における破壊エネルギーの
許容度が低くなるため、該部分での破壊が起こり易くな
り低温展開性が低下する傾向がある。Further, when the ratio between the tensile fracture strength and the flexural modulus is less than the above range, the strength is reduced due to the concentration of stress on the hinge portion and the mounting portion due to the deformation at the time of development, so that cracks and breakage are likely to occur. Deployment performance tends to decrease. On the other hand, if it exceeds the above range, the tensile elongation at break tends to decrease, and during deployment, stress concentration on the hinge portion and the mounting portion becomes difficult to be alleviated, cracking, breakage, etc. tend to occur, and the deployment performance tends to decrease. . In addition, if the Izod impact strength is less than the above range, the tolerance of fracture energy in a portion where stress concentration is likely to occur, such as a mounting portion or a portion having a hinge structure, becomes low during a low-temperature deployment test. In this case, breakage tends to occur in the portion, and low-temperature deployability tends to decrease.
【0033】[成形]乗物用エアバッグカバーの製造方
法としては、種々の成型法が適用可能であるが、通常は
射出成形法、又は、必要に応じて、ガスインジェクショ
ン成形法、射出圧縮成形法、ショートショット発泡成形
法等の成形法を用いるのが良い。射出成形を用いる場合
の成型条件としては、一般に100〜300℃、好まし
くは150〜280℃の成形温度、5〜100MPa、
好ましくは10〜80Mpaの射出圧力、20〜80
℃、好ましくは20〜60℃の金型温度で成形する。[Molding] As a method of manufacturing a vehicle airbag cover, various molding methods can be applied. Usually, an injection molding method or, if necessary, a gas injection molding method or an injection compression molding method is used. It is preferable to use a molding method such as a short shot foam molding method. As the molding conditions when using injection molding, generally, a molding temperature of 100 to 300 ° C., preferably 150 to 280 ° C., 5 to 100 MPa,
Preferably an injection pressure of 10 to 80 Mpa, 20 to 80
C., preferably at a mold temperature of 20-60.degree.
【0034】本発明の乗物用エアバッグカバーは、単層
射出成形品として用いても良いが、表皮層及び必要に応
じて合成樹脂発泡層を有した構造や、軟質ポリ塩化ビニ
ールやオレフィン系熱可塑性エラストマーの表皮層とポ
リオレフィン系樹脂の発泡層とからなる複合シートを真
空成形等にて賦形後、乗物用エアバッグカバーに接着さ
せる方法等があげられる。The vehicle airbag cover of the present invention may be used as a single-layer injection-molded product, but it may have a structure having a skin layer and, if necessary, a synthetic resin foam layer, or a soft PVC or olefin-based heat-resistant material. Examples include a method in which a composite sheet comprising a skin layer of a plastic elastomer and a foamed layer of a polyolefin-based resin is shaped by vacuum molding or the like, and then adhered to a vehicle airbag cover.
【0035】[用途]この様にして得られた乗物用エア
バッグカバーは、自動車等の高速移動体が衝突事故等の
際に、その衝撃や変形を感知することにより作動し、膨
張展開する乗物用エアバッグシステムのエアバッグ収納
用カバーとして用いられる。特に、フロントピラー、サ
イドピラー、リアピラー等のように細い枠部分に取り付
けられ、作動時にカバーが割れずに、開くように作動す
るカバーに適している。[Use] The vehicle airbag cover thus obtained is operated by sensing the impact or deformation of a high-speed moving body such as an automobile in the event of a collision or the like, and the vehicle is inflated and deployed. Used as an airbag storage cover for an airbag system. In particular, it is suitable for a cover that is attached to a thin frame portion such as a front pillar, a side pillar, a rear pillar, or the like, and that operates to open without opening the cover during operation.
【0036】[0036]
【実施例】本発明の乗物用エアバッグカバーを更に詳細
に説明するために、以下に実験例を示して具体的に説明
する。 [1]原材料 実施例及び比較例においては、下記に示す原材料を用い
た。DESCRIPTION OF THE PREFERRED EMBODIMENTS In order to explain the vehicle airbag cover of the present invention in more detail, an experimental example will be specifically described below. [1] Raw materials In the examples and comparative examples, the following raw materials were used.
【0037】[0037]
【表1】 [Table 1]
【0038】[0038]
【表2】 [Table 2]
【0039】[0039]
【表3】 [Table 3]
【0040】[0040]
【表4】 [Table 4]
【0041】[2]評価方法 これら実施例及び比較例における各種の評価は、以下に
示す通りの方法で行なった。但し、(2)〜(5)にお
ける測定試料は、インラインスクリュータイプ射出成形
機(日本製鋼所(株)製射出成形機;N100B)を用
いて、射出圧力50MPa、射出温度220℃、金型温
度40℃にて成形したピースを用いた。また、下記
(6)における測定試料は、インラインスクリュータイ
プ射出成形機(東芝機械(株)製射出成形機:IS22
0)を用いて、220℃の温度で成形した乗物用エアバ
ッグのモデル製品を用いた。[2] Evaluation method Various evaluations in these examples and comparative examples were performed by the following methods. However, the measurement samples in (2) to (5) were obtained by using an in-line screw type injection molding machine (injection molding machine manufactured by Nippon Steel Works Co., Ltd .; N100B) at an injection pressure of 50 MPa, an injection temperature of 220 ° C., and a mold temperature. A piece molded at 40 ° C. was used. The measurement sample in the following (6) is an in-line screw type injection molding machine (Injection molding machine IS22 manufactured by Toshiba Machine Co., Ltd.).
0), a model product of a vehicle airbag molded at a temperature of 220 ° C. was used.
【0042】(1)メルトフローレート(g/10分) JIS−K−6758に準拠して温度230℃、荷重2
1.17Nにて測定。 (2)曲げ弾性率(MPa) JIS−K−7203に準拠してスパン間64mm、曲
げ速度2mm/minにて測定。 (3)引張破壊強さ(MPa) JIS−K−7113に準拠し、長さ120mm、幅8
0mm、厚み2mmのシートから打ち抜いたJIS 2
号ダンベルを用い、引張スピード50mm/minにて
測定を実施した。 (4)アイゾット衝撃強さ(KJ/m2) JIS−K−7110に準拠したノッチ付き試験片を用
い−30℃にて測定。(1) Melt flow rate (g / 10 min) Temperature 230 ° C., load 2 according to JIS-K-6758
1.Measured at 17N. (2) Flexural modulus (MPa) Measured at a span of 64 mm and a bending speed of 2 mm / min according to JIS-K-7203. (3) Tensile fracture strength (MPa) According to JIS-K-7113, length 120 mm, width 8
JIS 2 punched from a 0 mm, 2 mm thick sheet
Using a No. dumbbell, the measurement was performed at a tensile speed of 50 mm / min. (4) Izod impact strength (KJ / m 2 ) Measured at −30 ° C. using a notched specimen in accordance with JIS-K-7110.
【0043】(5)耐熱変形性 JIS−K−7116に準拠した曲げクリープ試験治具
を用い、曲げ弾性率評価用試験片の幅方向(10mm
幅)を荷重に対して平行にして測定。110℃雰囲気下
で2.2MPaの荷重を加えた時の変形量が4mm以下
のものを耐熱変形性良好とした。 (6)成形性 220℃の成形温度で乗物用エアバッグのモデル製品が
ショートショットとなったものを不良とした。 (7)製品不良 成形した乗物用エアバッグのモデル製品の外観にヒケ、
フローマークの発生が著しいものについては不良とし
た。(5) Heat Deformation Resistance Using a bending creep test jig in accordance with JIS-K-7116, the width direction of the test piece for bending elastic modulus evaluation (10 mm
Width) parallel to the load. Those having a deformation amount of 4 mm or less when a load of 2.2 MPa was applied in an atmosphere of 110 ° C. were regarded as having good heat deformation resistance. (6) Formability A model product of a vehicle airbag which was short shot at a molding temperature of 220 ° C. was regarded as defective. (7) Product defect The appearance of the model product of the molded vehicle airbag has sink marks.
If a flow mark was remarkably generated, it was determined to be defective.
【0044】[3]実験例 実施例1〜16及び比較例1〜2 表1〜4に示す原材料を用い、表5〜8に示す配合組成
(重量部)にて配合し、この表5〜7に示す配合組成の
合計量100重量部に対して、フェノール系酸化防止剤
(商品名「イルガノックス1010」)0.1重量部を
添加し、L/D=33、シリンダー径45mmの二軸押
出機(池貝製PCM45)にて200℃の温度に設定し
て溶融混練しペレットを得た。また実施例10について
は上記添加剤以外に架橋剤として2,5−ジメチル−
2,5−ジ(t−ブチルパーオキシ)ヘキサン、2,5
−ジメチル−2,5−ジ(t−ブチルパーオキシ)−3
−ヘキシン(化薬アクゾ社製「カヤヘキサAD」)を
0.1重量部、架橋助剤としてトリメチロールプロパン
トリメタクリレート(三菱レイヨン社製「アクリルエス
テルTMP」)を0.2重量部添加し上記と同様の方法
にてペレットを得た。このペレットを上記の通り射出成
形して、上記の評価を行なった。これらの評価結果を表
5〜8に示す。[3] Experimental Examples Examples 1 to 16 and Comparative Examples 1 to 2 The raw materials shown in Tables 1 to 4 were used and blended in the composition shown in Tables 5 to 8 (parts by weight). 0.1 parts by weight of a phenolic antioxidant (trade name “Irganox 1010”) was added to 100 parts by weight of the total amount of the composition shown in 7, and a biaxial with L / D = 33 and a cylinder diameter of 45 mm The extruder (PCM45 made by Ikegai) was set at a temperature of 200 ° C. and melt-kneaded to obtain pellets. In Example 10, in addition to the above additives, 2,5-dimethyl-
2,5-di (t-butylperoxy) hexane, 2,5
-Dimethyl-2,5-di (t-butylperoxy) -3
-0.1 part by weight of hexine ("Kayahexa AD" manufactured by Kayaku Akzo) and 0.2 part by weight of trimethylolpropane trimethacrylate ("acrylic ester TMP" manufactured by Mitsubishi Rayon Co.) as a crosslinking aid were added. Pellets were obtained in the same manner. The pellets were injection molded as described above and evaluated as described above. Tables 5 to 8 show these evaluation results.
【0045】[0045]
【表5】 [Table 5]
【0046】[0046]
【表6】 [Table 6]
【0047】[0047]
【表7】 [Table 7]
【0048】[0048]
【表8】 [Table 8]
【0049】実施例17〜43 実施例1〜16の組成物に対し、表9の無機充填剤を配
合した評価結果を表10、11に示す。Examples 17 to 43 Tables 10 and 11 show the evaluation results obtained by blending the inorganic fillers shown in Table 9 with the compositions of Examples 1 to 16.
【0050】[0050]
【表9】 [Table 9]
【0051】[0051]
【表10】 [Table 10]
【0052】[0052]
【発明の効果】本発明は、エアバッグ膨張時に破壊、飛
散が無く、且つ、剛性感、耐熱変形性に優れたインスト
ルメントパネル内やフロントおよびサイドピラー等に設
置される乗物用エアバッグカバーを得ることができるの
で、自動車等の衝突事故の際に、その衝突や変形を感知
し、膨張するエアバッグ装置のカバー(蓋)として有用
なものである。According to the present invention, there is provided a vehicle airbag cover to be installed in an instrument panel, front and side pillars, etc., which does not break or scatter when the airbag is inflated, and has excellent rigidity and heat-resistant deformation. Since it can be obtained, it is useful as a cover (lid) of an airbag device that senses the collision and deformation in the event of a collision of an automobile or the like and inflates.
フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) //(C08L 23/00 (C08L 23/00 23:08 23:08 25:04 25:04 53:02) 53:02) Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat II (reference) // (C08L 23/00 (C08L 23/00 23:08 23:08 25:04 25:04 53:02) 53: 02)
Claims (10)
重量%となるように配合され、且つ、メルトフローレー
トが5g/10分以上、曲げ弾性率が550MPa以上
800MPa未満の物性を有する熱可塑性エラストマー
を成形してなる乗物用エアバッグカバー。 成分(A):オレフィン系樹脂55〜80重量%、 成分(B):エチレンと炭素原子数が6以上のα−オレ
フィンとの共重合体ゴム20〜45重量%1. The total of the following components (A) and (B) is 100
A vehicle airbag cover formed by molding a thermoplastic elastomer having physical properties of a melt flow rate of 5 g / 10 min or more and a flexural modulus of 550 MPa to less than 800 MPa. Component (A): 55 to 80% by weight of an olefin resin, Component (B): 20 to 45% by weight of a copolymer rubber of ethylene and an α-olefin having 6 or more carbon atoms
曲げ弾性率の比が0.03〜0.07である、請求項1
に記載の乗物用エアバッグカバー。2. The thermoplastic elastomer according to claim 1, wherein the ratio between the tensile fracture strength and the flexural modulus of the thermoplastic elastomer is 0.03 to 0.07.
2. The vehicle airbag cover according to claim 1.
強さが25KJ/m 2以上である、請求項1又は2に記
載の乗物用エアバッグカバー。3. Izod impact of thermoplastic elastomer
Strength is 25KJ / m TwoThe above is described in claim 1 or 2.
Vehicle airbag cover.
強さが30KJ/m 2以上である、請求項3に記載の乗
物用エアバッグカバー。4. Izod impact of thermoplastic elastomer
Strength is 30KJ / m TwoThe power according to claim 3, which is the above.
Airbag cover for goods.
フィンとの共重合体ゴム25〜45重量%、である、請
求項1〜4の何れかに記載の乗物用エアバッグカバー。5. The composition of a thermoplastic elastomer comprising: component (A): 55 to 75% by weight of an olefin resin; and component (B): a copolymer rubber of ethylene and an α-olefin having 6 or more carbon atoms. The vehicle airbag cover according to any one of claims 1 to 4, which is 25 to 45% by weight.
を満足する、請求項1〜5の何れかに記載の乗物用エア
バッグカバー。 成分(A):メルトフローレートが10〜100g/1
0分、エチレン含量が10%以下であり、重量平均分子
量(Mw)と数平均分子量(Mn)の比が5〜10であ
る、プロピレン・エチレンブロック共重合体、 成分(B):メルトフローレートが10g/10分以
下、密度が0.88g/cm3以下である、エチレンと
炭素原子数が6以上のα−オレフィンとの共重合体6. The vehicle airbag cover according to claim 1, wherein the component (A) and the component (B) satisfy the following physical properties. Component (A): melt flow rate is 10 to 100 g / 1.
0 minute, a propylene / ethylene block copolymer having an ethylene content of 10% or less and a ratio of weight average molecular weight (Mw) to number average molecular weight (Mn) of 5 to 10, Component (B): melt flow rate Is a copolymer of ethylene and an α-olefin having 6 or more carbon atoms having a density of 0.88 g / cm 3 or less.
0重量部に対し、下記成分(C)を更に含む、請求項1
〜6の何れかに記載の乗物用エアバッグカバー。 成分(C):密度が0.87g/cm3以下のエチレン
と炭素原子数が4以下のα−オレフィンとの共重合体1
〜20重量部7. A total of 10 of component (A) and component (B)
2. The composition according to claim 1, further comprising the following component (C) based on 0 parts by weight.
7. The vehicle airbag cover according to any one of claims 6 to 6. Component (C): Copolymer 1 of ethylene having a density of 0.87 g / cm 3 or less and α-olefin having 4 or less carbon atoms
~ 20 parts by weight
0重量部に対し、下記成分(D)を更に含む、請求項1
〜7の何れかに記載の乗物用エアバッグカバー。 成分(D):スチレン系エラストマー1〜20重量部8. A total of 10 of component (A) and component (B)
2. The composition according to claim 1, further comprising the following component (D) based on 0 parts by weight.
8. The vehicle airbag cover according to any one of claims 7 to 7. Component (D): 1 to 20 parts by weight of a styrene elastomer
芳香族ビニル−共役ジエンブロック共重合体ゴムの水素
添加物である、請求項8に記載の乗物用エアバッグカバ
ー。9. The vehicle airbag cover according to claim 8, wherein the styrene elastomer of the component (D) is a hydrogenated product of an aromatic vinyl-conjugated diene block copolymer rubber.
ー、及びリアピラーのいずれかに設置される、請求項1
〜9の何れかに記載の乗物用エアバッグカバー。10. The vehicle according to claim 1, which is installed on one of a front pillar, a side pillar, and a rear pillar of the automobile.
10. The vehicle airbag cover according to any one of claims 9 to 9.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000324901A JP2001206183A (en) | 1999-11-18 | 2000-10-25 | Air bag cover for vehicle |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32849899 | 1999-11-18 | ||
JP11-328498 | 1999-11-18 | ||
JP2000324901A JP2001206183A (en) | 1999-11-18 | 2000-10-25 | Air bag cover for vehicle |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2001206183A true JP2001206183A (en) | 2001-07-31 |
Family
ID=26572894
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000324901A Pending JP2001206183A (en) | 1999-11-18 | 2000-10-25 | Air bag cover for vehicle |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2001206183A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008013757A (en) * | 2006-06-05 | 2008-01-24 | Toyota Motor Corp | Polypropylene resin composition and injection molded article for automobile use |
JP2008045038A (en) * | 2006-08-17 | 2008-02-28 | Sumitomo Chemical Co Ltd | Air bag cover form |
JP2008045037A (en) * | 2006-08-17 | 2008-02-28 | Sumitomo Chemical Co Ltd | Air bag cover form |
JP2013035888A (en) * | 2011-08-03 | 2013-02-21 | Mitsubishi Chemicals Corp | Thermoplastic elastomer composition and air bag housing cover |
WO2014046139A1 (en) * | 2012-09-19 | 2014-03-27 | 三菱化学株式会社 | Airbag housing cover |
JP7571559B2 (en) | 2021-01-15 | 2024-10-23 | Mcppイノベーション合同会社 | Airbag storage cover |
-
2000
- 2000-10-25 JP JP2000324901A patent/JP2001206183A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008013757A (en) * | 2006-06-05 | 2008-01-24 | Toyota Motor Corp | Polypropylene resin composition and injection molded article for automobile use |
JP2008045038A (en) * | 2006-08-17 | 2008-02-28 | Sumitomo Chemical Co Ltd | Air bag cover form |
JP2008045037A (en) * | 2006-08-17 | 2008-02-28 | Sumitomo Chemical Co Ltd | Air bag cover form |
JP2013035888A (en) * | 2011-08-03 | 2013-02-21 | Mitsubishi Chemicals Corp | Thermoplastic elastomer composition and air bag housing cover |
WO2014046139A1 (en) * | 2012-09-19 | 2014-03-27 | 三菱化学株式会社 | Airbag housing cover |
JP7571559B2 (en) | 2021-01-15 | 2024-10-23 | Mcppイノベーション合同会社 | Airbag storage cover |
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