JPH01141143A - Constrained material for vehicle - Google Patents
Constrained material for vehicleInfo
- Publication number
- JPH01141143A JPH01141143A JP29609187A JP29609187A JPH01141143A JP H01141143 A JPH01141143 A JP H01141143A JP 29609187 A JP29609187 A JP 29609187A JP 29609187 A JP29609187 A JP 29609187A JP H01141143 A JPH01141143 A JP H01141143A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- constrained
- damping
- base material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 76
- 229920005989 resin Polymers 0.000 claims abstract description 39
- 239000011347 resin Substances 0.000 claims abstract description 39
- 238000013016 damping Methods 0.000 claims abstract description 31
- 239000003365 glass fiber Substances 0.000 claims abstract description 7
- 230000000452 restraining effect Effects 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
- 239000005977 Ethylene Substances 0.000 claims description 7
- 238000002156 mixing Methods 0.000 abstract description 6
- 238000010438 heat treatment Methods 0.000 abstract description 5
- 230000004927 fusion Effects 0.000 abstract description 4
- 239000000470 constituent Substances 0.000 abstract 2
- 239000003981 vehicle Substances 0.000 description 13
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 10
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 10
- 229910000831 Steel Inorganic materials 0.000 description 10
- -1 glycerin ester Chemical class 0.000 description 10
- 239000010959 steel Substances 0.000 description 10
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 10
- 238000009826 distribution Methods 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 8
- 239000010426 asphalt Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 6
- 238000000465 moulding Methods 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 235000007586 terpenes Nutrition 0.000 description 4
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000007591 painting process Methods 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000010734 process oil Substances 0.000 description 3
- 150000003505 terpenes Chemical class 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- 239000004641 Diallyl-phthalate Substances 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-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
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 description 1
- GPZYYYGYCRFPBU-UHFFFAOYSA-N 6-Hydroxyflavone Chemical compound C=1C(=O)C2=CC(O)=CC=C2OC=1C1=CC=CC=C1 GPZYYYGYCRFPBU-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 240000000972 Agathis dammara Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002871 Dammar gum Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 244000117054 Rungia klossii Species 0.000 description 1
- 235000002492 Rungia klossii Nutrition 0.000 description 1
- KRADHMIOFJQKEZ-UHFFFAOYSA-N Tri-2-ethylhexyl trimellitate Chemical compound CCCCC(CC)COC(=O)C1=CC=C(C(=O)OCC(CC)CCCC)C(C(=O)OCC(CC)CCCC)=C1 KRADHMIOFJQKEZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001278 adipic acid derivatives Chemical class 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- WXZOXVVKILCOPG-UHFFFAOYSA-N bis(2-ethylhexyl) benzene-1,3-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC(C(=O)OCC(CC)CCCC)=C1 WXZOXVVKILCOPG-UHFFFAOYSA-N 0.000 description 1
- ZVPBHZIVOWGPMT-UHFFFAOYSA-N bis(2-ethylhexyl) cyclohexene-1,2-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=C(C(=O)OCC(CC)CCCC)CCCC1 ZVPBHZIVOWGPMT-UHFFFAOYSA-N 0.000 description 1
- XRFYGUOAWVKOCQ-UHFFFAOYSA-N bis(8-methylnonyl) cyclohex-4-ene-1,2-dicarboxylate Chemical compound CC(C)CCCCCCCOC(=O)C1CC=CCC1C(=O)OCCCCCCCC(C)C XRFYGUOAWVKOCQ-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical class OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000007499 fusion processing Methods 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical class [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003329 sebacic acid derivatives Chemical class 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- FJFYFBRNDHRTHL-UHFFFAOYSA-N tris(8-methylnonyl) benzene-1,2,4-tricarboxylate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC(C)C)C(C(=O)OCCCCCCCC(C)C)=C1 FJFYFBRNDHRTHL-UHFFFAOYSA-N 0.000 description 1
- WGKLIJDVPACLGG-UHFFFAOYSA-N trizinc diborate hydrate Chemical compound O.[Zn++].[Zn++].[Zn++].[O-]B([O-])[O-].[O-]B([O-])[O-] WGKLIJDVPACLGG-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R13/00—Elements for body-finishing, identifying, or decorating; Arrangements or adaptations for advertising purposes
- B60R13/08—Insulating elements, e.g. for sound insulation
Landscapes
- Physics & Mathematics (AREA)
- Acoustics & Sound (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
- Body Structure For Vehicles (AREA)
- Vibration Prevention Devices (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、車輌の床板、計器盤等の振動し易い振動基材
上にサンドイッチ型の制振構造を形成するに当って、制
振材を挟装して積層される拘束材に関する。Detailed Description of the Invention (Industrial Application Field) The present invention provides a method for forming a sandwich-type vibration damping structure on a vibrating base material that easily vibrates, such as a floorboard or an instrument panel of a vehicle. This invention relates to a restraining material that is sandwiched and laminated.
(従来の技術)
車輌の床板あるいはダツシュボードなどの振動基材面に
は、アスファルトを主成分とする熱融着性制振材が融着
されて使用されることが多い。(Prior Art) A heat-fusible vibration damping material containing asphalt as a main component is often fused to the surface of a vibrating base material such as a vehicle floorboard or dash board.
また、近年ではアスファルト系制振材の上面に拘束材と
して鋼、アルミニウムなどの金属シートを設け、あるい
はエポキシ樹脂、ジアリルフタレート樹脂、アクリル樹
脂などの熱硬化性樹脂を積層することによりサンドイン
チ構造として制振性能を向上させることも行なわれてい
る。(たとえば、特開昭58−63542、特開昭62
−19445など)
(発明が解決しようとする問題点)
しかしながら、これらの割振構造には以下の問題がある
。すなわち、アスファルトなどを主成分とする熱融着性
制振シートのみで振動基材の割振を図るダブルレイヤー
型制振構造では、その割振性能を向上させるには厚みを
増大させる必要があり、これは車輌重量を増大させると
ともにコストも増大させることになる。また、アスファ
ルト系熱融着性制振シートの上面に鋼板、アルミニウム
板等を積層するサンドイッチ型割振構造の場合には構造
としての割振性能は向上するが、拘束層として剛性の高
い金属板を熱融着性制振シート上に密着させるため、例
えば鋼板等の高剛性の振動基材に対して機械的に固定し
たり、あるいはボルト等を用いてねじ止めするなどによ
り固定する必要がある。ところが、一般に車輌の床板等
は剛性付与の目的で凹凸形状にプレス成形されているた
め、拘束用金属板をこれと相補的な形状に成形しておく
必要があり、余分の工程が必要であるほか取り付けに際
して所定位置に正しく位置決めすることが容易でないと
いう問題がある。In addition, in recent years, a metal sheet such as steel or aluminum is provided as a restraining material on the top surface of asphalt-based vibration damping material, or a sandwich structure is created by laminating thermosetting resin such as epoxy resin, diallyl phthalate resin, or acrylic resin. Efforts are also being made to improve vibration damping performance. (For example, JP-A-58-63542, JP-A-62
-19445, etc.) (Problems to be Solved by the Invention) However, these allocation structures have the following problems. In other words, in a double-layer damping structure in which the vibration base material is distributed using only a heat-adhesive damping sheet whose main component is asphalt, it is necessary to increase the thickness in order to improve its distribution performance. This increases vehicle weight and costs as well. In addition, in the case of a sandwich-type distribution structure in which steel plates, aluminum plates, etc. are laminated on the top surface of an asphalt-based heat-adhesive vibration damping sheet, the distribution performance as a structure improves; In order to adhere closely to the fusible damping sheet, it is necessary to fix it mechanically to a highly rigid vibration base material such as a steel plate, or by screwing it with bolts or the like. However, since the floorboards of vehicles are generally press-formed into an uneven shape for the purpose of imparting rigidity, it is necessary to form the restraining metal plate into a complementary shape, which requires an extra process. Another problem is that it is not easy to correctly position the device at a predetermined position during installation.
また、未硬化の熱硬化性樹脂を制振層上に載置し塗装す
る工程で硬化させて拘束層として使用する方法は前記の
不都合はないものの、未硬化の熱硬化性樹脂自身が保存
中に硬化反応を起すために気温の高くなる様なときには
長期間の保存ができないという問題があり、更に硬化に
際して反応が早すぎると床板等の凹凸形状に追従できな
かったり割振層との融着不良を生ずるなどの欠陥を生じ
、制振特性を損なうなどの問題もあった。In addition, although the method of placing an uncured thermosetting resin on the damping layer and curing it during the painting process and using it as a restraining layer does not have the above disadvantages, the uncured thermosetting resin itself is stored during storage. There is a problem that it cannot be stored for a long time when the temperature is high because a curing reaction occurs, and furthermore, if the reaction is too fast during curing, it may not be able to follow the uneven shape of floorboards, etc., or it will not adhere well to the distribution layer. There were also problems such as defects such as , resulting in damage to vibration damping characteristics.
(問題点を解決するための手段)
本発明はこのような問題点を改良したものであって、車
輌等における振動基材上に制振材を挟装して積層される
拘束材であって、粘着付与樹脂100重量部に対してエ
チレン系樹脂3〜100重量部およびガラス繊維3〜7
5重量部を少くとも配合してなる組成物で形成されたこ
とを特徴とする拘束材を要旨とするものである。(Means for Solving the Problems) The present invention improves these problems, and is a restraining material in which a damping material is sandwiched and laminated on a vibration base material in a vehicle, etc. , 3 to 100 parts by weight of ethylene resin and 3 to 7 parts by weight of glass fiber per 100 parts by weight of tackifier resin.
The gist of the present invention is a restraining material characterized by being formed from a composition containing at least 5 parts by weight.
ここで本発明の拘束材は、弾性率が高く、耐久性に優れ
、軽量で、かつこの種の車輌用として、塗装工程等での
加熱処理によって凹凸ある振動基材に完全に密着する必
要があり、しかも比較的高温でも弾性率の低下が少なく
、加工性も良好であること等が好ましい性状として要求
される。本発明に係る拘束材はこれらの諸要求を、10
0重量部の粘着付与樹脂に対して少なくとも3〜100
重量部のエチレン系樹脂と3〜75重量部のガラス繊維
とを配合した組成物から形成することにより満したもの
である。Here, the restraining material of the present invention has a high elastic modulus, is excellent in durability, is lightweight, and is required for use in this type of vehicle to completely adhere to the uneven vibrating base material by heat treatment during the painting process etc. In addition, preferred properties include a small decrease in elastic modulus even at relatively high temperatures and good workability. The restraining material according to the present invention satisfies these requirements by 10
At least 3 to 100 parts by weight of tackifying resin
This is achieved by forming a composition containing 3 parts by weight of an ethylene resin and 3 to 75 parts by weight of glass fiber.
本発明に用いられる粘着付与樹脂は、ロジン、ダンマル
等の天然樹脂、重合ロジン、部分水添ロジン等の変成ロ
ジン、グリセリンエステルロジン、ペンタエリスリット
エステルロジン等のロジンや変成ロジンの誘導体、β−
ピネンの重合体等のポリチルヘンl Jll 、テルペ
ンフェノール等のテ゛ルペン変成体、シクロペンタジェ
ン樹脂、芳香族系石tUt脂、アルキルフェノール−ア
セチレン樹脂、キシレン系樹脂、クマゝロンインデン樹
脂、ビニルトルエン−αメチルスチレン共重合樹脂等の
樹脂状の粘着付与剤であって軟化点が少くとも60〜1
80℃のものである。これらの粘着付与樹脂は、1種又
は2種以上のものを混合して使用することができる。The tackifying resin used in the present invention includes natural resins such as rosin and dammar, modified rosins such as polymerized rosin and partially hydrogenated rosin, derivatives of rosins and modified rosins such as glycerin ester rosin and pentaerythritol ester rosin, and β-
Polymers such as pinene polymers, modified terpenes such as terpene phenols, cyclopentadiene resins, aromatic stone fats, alkylphenol-acetylene resins, xylene resins, coumaron indene resins, vinyltoluene-α-methylstyrene A resinous tackifier such as a copolymer resin with a softening point of at least 60 to 1
It is at 80°C. These tackifying resins can be used alone or in combination of two or more.
これらの粘着付与樹脂の軟化点は60℃〜180℃であ
ることが必要であるが、更に好ましくは80℃〜140
℃である。60℃未満であると車輌のサンドインチ型割
振構造の拘束材として機能する温度領域が狭く、車輌の
実使用温度範囲でも流動を生じるという不都合が生じる
。さらに車輌への制振材取付工程は通常120℃〜15
0℃、30分程度の条件となる塗料焼付工程を利用して
行なわれるが、60℃未満の軟化点のものでは不均一な
流動を生じて均質な厚さの拘束構造が得られなくなる。The softening point of these tackifying resins is required to be 60°C to 180°C, more preferably 80°C to 140°C.
It is ℃. If the temperature is less than 60° C., the temperature range in which it functions as a restraining material for the sandwich-type distribution structure of the vehicle is narrow, resulting in the disadvantage that flow occurs even in the actual operating temperature range of the vehicle. Furthermore, the process of attaching vibration damping material to a vehicle is usually at 120°C to 15°C.
This is carried out using a paint baking process at 0°C for about 30 minutes, but if the softening point is less than 60°C, non-uniform flow will occur and a constrained structure with a uniform thickness will not be obtained.
また逆に、180℃以上であれば塗料焼付工程の条件で
は割振材との融着が不充分になるとともに鋼板の凹凸に
対して追従しなくなり、良好な制振特性が得られなくな
るばかりでなく外観も極めて悪くなる。On the other hand, if it is above 180°C, under the conditions of the paint baking process, the fusion with the damping material will be insufficient and it will not follow the unevenness of the steel plate, which will not only make it impossible to obtain good vibration damping properties. The appearance will also be extremely poor.
本発明で配合されるエチレン系樹脂は、粘着付与樹脂の
強度的脆さを改良する目的で配合するものであり、ポリ
エチレン、エチレン−酢酸ビニル共重合体(EVA)、
エチレン−エチルアクリレート共重合体(EEA) 、
エチレン−アクリル酸共重合体、ならびにエチレンと共
重合可能な不飽和カルボン酸またはその塩ないしはその
エステルとエチレンとの共重合体から選ばれたものであ
る。The ethylene resin blended in the present invention is blended for the purpose of improving the strength and brittleness of the tackifier resin, and includes polyethylene, ethylene-vinyl acetate copolymer (EVA),
Ethylene-ethyl acrylate copolymer (EEA),
It is selected from ethylene-acrylic acid copolymers and copolymers of ethylene and unsaturated carboxylic acids copolymerizable with ethylene, salts thereof, or esters thereof.
これらの中では、とくに酢酸ビニル共重合量が3〜25
%、メルトインデックス0.5〜450のEVAが好ま
しく、制振材との熱融着性、高温での溶融粘度、拘束材
としての強度性能などの点から優れている。Among these, especially the amount of vinyl acetate copolymerized is 3 to 25
% and a melt index of 0.5 to 450 is preferable, and is excellent in terms of heat fusion properties with damping materials, melt viscosity at high temperatures, strength performance as a restraining material, etc.
かかるエチレン系樹脂の配合量は、他の配合剤の使用量
にもよるが、粘着付与樹脂100重量部に対し3〜10
0重量部、好ましくは5〜50重量部である。3重量部
以下では前述のような性能の改良がなく、100重量部
を越えると成形品の弾性率が低下しサンドインチ型制振
構造における拘束材としての機能を果さなくなる。The amount of the ethylene resin blended is 3 to 10 parts by weight per 100 parts by weight of the tackifying resin, although it depends on the amount of other compounding agents used.
0 parts by weight, preferably 5 to 50 parts by weight. If the amount is less than 3 parts by weight, there will be no improvement in performance as described above, and if it exceeds 100 parts by weight, the elastic modulus of the molded product will decrease and it will no longer function as a restraining material in a sandwich-type vibration damping structure.
本発明で配合されるガラス繊維は、その径および長さは
特に限定されるものではないが、通常は長さが100m
m以下、好ましくは25龍以下のチョップトストランド
繊維が使用される。100鶴以上の長さの繊維を使用し
ても強度的な改良は認められないばかりでなく、混合す
る際に破断する繊維が多々生じるとともに、均一な分散
状態を得に(いことがあるからである。また、その使用
量は他の配合剤の使用量にもよるが、粘着付与樹脂10
0重量部に対し3〜75重量部、好ましくは5〜50重
量部である。3重量部以下では強度改良効果はあまり期
待できず、75重量部を越えると成形時の粘度が著しく
上昇して加工困難となるから好ましくない。The diameter and length of the glass fibers blended in the present invention are not particularly limited, but the length is usually 100 m.
Chopped strand fibers of less than 25 m, preferably less than 25 m, are used. Even if fibers with a length of 100 Tsuru or more are used, not only no improvement in strength is observed, but also many fibers break during mixing, and it may be difficult to obtain a uniform dispersion state. Although the amount used depends on the amount of other ingredients used, the tackifying resin 10
The amount is 3 to 75 parts by weight, preferably 5 to 50 parts by weight relative to 0 parts by weight. If it is less than 3 parts by weight, no significant strength improvement effect can be expected, and if it exceeds 75 parts by weight, the viscosity during molding will increase significantly and processing will become difficult, which is not preferable.
本発明の組成物においては、前記配合剤の他に、拘束材
としての性能を損わない程度の弾性率の低下の範囲内で
成形性の改良や熱融着性の改良などの目的で、可塑剤を
添加することができる。In the composition of the present invention, in addition to the above-mentioned compounding agents, for the purpose of improving moldability and heat-fusibility within the range of reducing the elastic modulus to an extent that does not impair the performance as a restraining material, Plasticizers can be added.
これらの可塑剤としては、ジメチルフタレート、ジブチ
ルフタレート、ジ(2エチルヘキシル)フタレート、そ
の他の高級アルコールフタレート等のフタル酸誘導体、
ジメチルイソフタレート、ジ(2エチルヘキシル)イソ
フタレート等のイソフタル酸誘導体、ジ(2エチルヘキ
シル)テトラヒドロフタレート、ジイソデシルテトラヒ
ドロフタレート等のテトラヒドロフタル酸誘導体、ジ(
2エチルヘキシル)アジペート、ジイソデシルアジペー
ト、ジイソノニルアジペート等のアジピン酸誘導体、ジ
ブチルフタレート、ジ(2エチルヘキシル)セバケート
等のセバシン酸誘導体、トリ(2工、チルヘキシル)ト
リメリテート、トリイソデシルトリメリテート等のトリ
メリット酸誘導体、くえん酸、イタコン酸、オレイン酸
等の有機酸のモノエステル誘導体やパラフィン誘導体、
エポキシ誘導体、ポリエステル重合型可塑剤等や、パラ
フィン系プロセスオイル、ナフテン系プロセスオイル、
芳香族系プロセスオイル等の鉱物油軟化剤、ひまし油、
綿実油、あまに油、なたね油、大豆油、パーム油、やし
油等の植物油系軟化剤等が挙げられ、これらの中から1
種または2種以上を混合して添加することができる。These plasticizers include phthalic acid derivatives such as dimethyl phthalate, dibutyl phthalate, di(2ethylhexyl) phthalate, and other higher alcohol phthalates;
Isophthalic acid derivatives such as dimethyl isophthalate and di(2ethylhexyl)isophthalate; tetrahydrophthalic acid derivatives such as di(2ethylhexyl)tetrahydrophthalate and diisodecyltetrahydrophthalate;
Adipic acid derivatives such as 2-ethylhexyl) adipate, diisodecyl adipate, diisononyl adipate, sebacic acid derivatives such as dibutyl phthalate, di(2-ethylhexyl) sebacate, trimellitate such as tri(2-ethylhexyl) trimellitate, triisodecyl trimellitate, etc. Acid derivatives, monoester derivatives of organic acids such as citric acid, itaconic acid, and oleic acid, and paraffin derivatives;
Epoxy derivatives, polyester polymerization plasticizers, paraffinic process oils, naphthenic process oils, etc.
Mineral oil softeners such as aromatic process oils, castor oil,
Vegetable oil softeners such as cottonseed oil, linseed oil, rapeseed oil, soybean oil, palm oil, and coconut oil are listed, and one of these
A species or a mixture of two or more species can be added.
さらに本発明においては、炭酸カルシウム、タルク、ク
レー、硫酸カルシウム、硫酸バリウム等の無機充填剤、
ハロゲン化合物、アンチモン酸化物、ホウ酸亜鉛水和物
、水酸化アルミニウム等の難燃剤、熱安定剤、滑剤、ブ
ロッキング防止剤、着色剤、紫外線防止剤等を加えても
よい。また、軽量化を図るために、シラスバルーン、ガ
ラスバルーン、発泡石等の微小中空体などの充填材等も
使用することができる。Furthermore, in the present invention, inorganic fillers such as calcium carbonate, talc, clay, calcium sulfate, barium sulfate,
Flame retardants such as halogen compounds, antimony oxides, zinc borate hydrate, and aluminum hydroxide, heat stabilizers, lubricants, antiblocking agents, colorants, and ultraviolet inhibitors may be added. Further, in order to reduce the weight, fillers such as micro hollow bodies such as white glass balloons, glass balloons, and foamed stones can also be used.
本発明に係る拘束材の成形法は特に限定されないが、例
えば前記した粘着付与樹脂に所定の配合剤をバンバリー
ミキサ−、ヘンシェルミキサー、リボンブレンダー等の
各種のミキサー等によって加熱混合し、押出成形、ロー
ル成形、射出成形、プレス成形等によりシート状として
もよい。また特殊な成形法として、加熱混合可能な容器
中で溶融・混合し、この溶融組成物をスリット状のノズ
ル等から流動・滴下させてシート状としたり、ロールコ
ータ−やナイフコーターを用いてシート状に成形するこ
ともできる。加工中におけるガラス繊維等の切断、微小
中空体の破壊等の不都合を防止するためには、このよう
な大きな剪断力が作用しない混合方法を選択するのがよ
い。粘着付与樹脂は通常のポリエチレン、ポリプロピレ
ン、ポリ塩化ビニル等の樹脂類、あるいはブタジェンゴ
ム、イソプレンゴム等のゴム類と較べて溶融粘度が著る
しく低いため、押出成形、カンンダー成形等の強い剪断
力の作用する成形法を採らなくとも、単純な加熱溶融、
混合により配合剤を容易に均質分散させることができ、
そのままスリット状ノズルから流出させることによりシ
ートを得ることができる。The method of molding the restraining material according to the present invention is not particularly limited, but for example, the above-mentioned tackifying resin and a predetermined compounding agent are heated and mixed with various mixers such as a Banbury mixer, Henschel mixer, ribbon blender, etc., and extrusion molding, It may be formed into a sheet by roll molding, injection molding, press molding, or the like. In addition, special molding methods include melting and mixing in a container that can be heated and mixed, and then flowing and dripping this molten composition from a slit-shaped nozzle, etc. to form a sheet, or using a roll coater or knife coater to form a sheet. It can also be formed into a shape. In order to prevent inconveniences such as cutting of glass fibers and destruction of micro hollow bodies during processing, it is preferable to select a mixing method that does not apply such large shearing forces. Tackifying resins have significantly lower melt viscosity than ordinary resins such as polyethylene, polypropylene, and polyvinyl chloride, or rubbers such as butadiene rubber and isoprene rubber, so they cannot be used under strong shearing forces such as extrusion molding and candor molding. Simple heat melting,
By mixing, the ingredients can be easily dispersed homogeneously,
A sheet can be obtained by directly flowing out of the slit-shaped nozzle.
この様にして得られるシートの厚みは特に限定されるも
のではないが、車輌の床板等の上に形成されるサンドイ
ンチ型制振構造の拘束材として使うには、通常0.5〜
3n程度の範囲のもので充分である。The thickness of the sheet obtained in this way is not particularly limited, but it is usually 0.5 to
A range of about 3n is sufficient.
また本発明に係る拘束材の拘束層としての適用は、被割
振層となる車輌等の振動基材上に、例えばアスファルト
系等の熱融着型割振材のシートを介して本発明に係る拘
束材シートを積層載置し、その後の塗装工程などにおい
て加熱することによって振動基材に密着したサンドイッ
チ型の制振構造を強固なものとして構成することができ
る。Furthermore, the restraining material according to the present invention can be applied as a restraining layer by applying the restraining material according to the present invention to a vibration base material such as a vehicle, which is a layer to be distributed, through a sheet of a heat-sealing type distribution material such as asphalt. By stacking the material sheets and heating them in a subsequent coating process, etc., it is possible to form a strong sandwich-type vibration damping structure that is in close contact with the vibration base material.
(発明の効果)
以上説明したように、本発明に係る拘束材は、熱融着型
割振材とともに車輌等の振動基材上に載置し塗装工程等
において振動基材、熱融着型制振材及び拘束材を同時に
加熱することにより緊密に固定することができ、従って
金属板を拘束材として使用する場合のような工程数増が
ない、また本拘束材は熱溶融型であって、架橋反応等に
よる硬化を利用するものではないことから、熱硬化型樹
脂を含む拘束材のような硬化性能の経時的な変化もなく
長期間の保存に耐えるとともに、熱融着工程での割振材
との融着不良及び振動基材の凹凸形状に対する追従不良
も生ずることがなく、さらに得られるサンドインチ型制
振構造は広い温度範囲にわたって優れた割振作用を発揮
する等の特徴を有するものである。(Effects of the Invention) As explained above, the restraint material according to the present invention is placed on a vibrating base material such as a vehicle together with a heat-sealing type distribution material, and in a painting process etc. By heating the vibration material and the restraining material at the same time, they can be tightly fixed, so there is no increase in the number of steps unlike when using a metal plate as the restraining material, and this restraining material is a heat-melting type, Because it does not utilize curing through cross-linking reactions, etc., it can withstand long-term storage without any change in curing performance over time, unlike constraining materials containing thermosetting resins, and can be used as an allocation material in the heat fusion process. There is no problem of poor fusion with the vibration base material or poor tracking of the uneven shape of the vibrating base material, and the resulting sandwich-inch vibration damping structure exhibits excellent damping effects over a wide temperature range. .
11桝
第1表に示す各組成の材料を230℃に昇温したステン
レス容器中で溶融・混合し、得られた混合物をホットプ
レスして厚さ2鶴のシート状制振構造用拘束材を得た。The materials with the respective compositions shown in Table 1 were melted and mixed in a stainless steel container heated to 230°C, and the resulting mixture was hot pressed to form a sheet-like restraining material for vibration damping structures with a thickness of 2 mm. Obtained.
なお、数値の単位は重量部である。Note that the units of numerical values are parts by weight.
上記組成を有する各拘束材について下記各項目の試験を
行なった。The following tests were conducted on each restraining material having the above composition.
(al 加工性試験
第1表で示した試料Nal Nm9の組成物についてス
テンレス容器中での溶融・攪拌の容易さと混合物の分散
の程度、成形物の取扱いの容易さについて5段階で評価
した0判定基準は次のとおりである。(Al Workability test The composition of sample Nal Nm9 shown in Table 1 was evaluated on a five-point scale for ease of melting and stirring in a stainless steel container, degree of dispersion of the mixture, and ease of handling of molded products. The criteria are as follows.
(溶融・攪拌性)
5点:容易に溶融し、粘度低く攪拌極めて容易4点:溶
融性、溶融粘度いずれかが普通程度であるが溶融・攪拌
容易
3点:溶融性、溶融粘度とも普通であり溶融・攪拌可能
2点:溶融性、溶融粘度のいずれかが悪く溶融・攪拌に
難がある。(Melting/stirability) 5 points: Easily melted, low viscosity, very easy to stir 4 points: Either meltability or melt viscosity is normal, but easy to melt/stir 3 points: Both meltability and melt viscosity are normal. Yes, melting/stirring possible 2 points: Either meltability or melt viscosity is poor and melting/stirring is difficult.
1点:溶融が悪く、粘度が高く溶融・溶融攪拌が極めて
困難
(分散・取扱性)
5点二分散は均一であり成形品の強度高い4点:分散程
度、成形品強度いずれかが普通程度である。1 point: Poor melting, high viscosity, extremely difficult to melt and stir (dispersion/handling) 5 points: Bidispersion is uniform and the strength of the molded product is high 4 points: Either the degree of dispersion or the strength of the molded product is average It is.
3点:分散程度、成形品強度とも普通
2点二分散程度、成形品強度いずれかが悪く機能上問題
が生じる可能性がある。3 points: The degree of dispersion and the strength of the molded product are generally 2 points.The strength of the molded product is either poor and may cause functional problems.
1点二分散程度、成形品強度いずれも悪く機能上問題が
ある。Both the one-point bidispersity and the strength of the molded product are poor and there are functional problems.
加工性の基準としては、3点以上なら可能という判定で
ある。結果を第2表に示す。As a criterion for workability, it is determined that workability is possible if the workability is 3 or more points. The results are shown in Table 2.
溶融・撹拌性 345535221
分散・取扱性 455541352
(b) 割振性能試験
制振材としてアスファルト系制振シート(「メルシート
」、日本特殊塗料株式会社製厚さ2m)を用い、第1表
の拘束材および従来技術の拘束材をそれぞれ150X3
00 (龍)の鋼板(厚さ0゜8鰭)と組合せて割振構
造体を作成し、各構造体の損失係数を20℃、40℃、
60℃にて測定した。制振材と拘束材の貼合せは鋼板上
に制振材及び拘束材を積層し、150℃×30分の条件
のオーブン中で加熱処理を行い各層を融着させた。損失
係数は機械インピーダンスの共振点よりの半値巾から算
出し、内挿法により20011zの損失係数を求めた。Melting/stirring properties 345535221 Dispersion/handling properties 455541352 (b) Asphalt-based vibration damping sheet ("Melsheet", manufactured by Nippon Tokushu Toyo Co., Ltd., 2 m thick) was used as the vibration damping material in the allocation performance test, and the restraining materials and Conventional restraint material 150X3 each
00 (Dragon) steel plate (thickness: 0°, 8 fins) was used to create an allocation structure, and the loss coefficient of each structure was set at 20°C, 40°C,
Measured at 60°C. To bond the damping material and the restraining material, the damping material and the restraining material were laminated on a steel plate, and heat treatment was performed in an oven at 150° C. for 30 minutes to fuse each layer. The loss coefficient was calculated from the half-width from the resonance point of the mechanical impedance, and the loss coefficient of 20011z was determined by interpolation.
尚、測定周波数範囲は1〜100011zである。測定
結果を第3表に示す。Note that the measurement frequency range is 1 to 100011z. The measurement results are shown in Table 3.
なお、比較のために用いた拘束材は、それぞれ次の通り
のものである。The restraining materials used for comparison are as follows.
!1kLIO:厚さ0.8mの鋼板
−11:ブタジェンゴム1001ジアリルフタレート1
00、過酸化物(t−BPB)5、炭酸カルシウム10
0、カーボン5を混練し、ロールで厚さ2鰭のシートと
したもの。! 1kLIO: 0.8m thick steel plate-11: Butadiene rubber 1001 diallyl phthalate 1
00, peroxide (t-BPB) 5, calcium carbonate 10
0. Carbon 5 was kneaded and rolled into a sheet with a thickness of 2 fins.
第3表
1 0.2B 0.330.38
2 0.260.350.37
3 0.250.340.36
4 0.290.370.39
5 0.290.380.39
6“0.110.150.08
790.180.290.30
8” 0.110,120.08
9“0.210.330.35
10” 0.190,330.35
11” 0.180.250.30
なし” 0.10 0.06 0.04*は比較例で
ある。Table 3 1 0.2B 0.330.38 2 0.260.350.37 3 0.250.340.36 4 0.290.370.39 5 0.290.380.39 6"0.110. 150.08 790.180.290.30 8" 0.110,120.08 9"0.210.330.35 10" 0.190,330.35 11" 0.180.250.30 None" 0. 10 0.06 0.04* is a comparative example.
(C) 凹凸板への形状追従試験
前述のアスファルト系割振材および各拘束材を各々巾2
0+n、長さ250 mに切り出し、第1図に示す凹凸
波形状の鋼板上に波の方向と直交するように1ruiし
て150℃×30分の条件でオーブン中で加熱処理を行
い、凹凸形状への追従性を観察した。その結果を第4表
に示す。ただし、判定は隙間なく密着しているものを“
○”、隙間の残ったものを“×”とした。(C) Shape following test on uneven board The above-mentioned asphalt-based distribution material and each restraint material were each
0+n, length 250 m, placed on a steel plate with an uneven corrugated shape shown in Fig. 1 for 1 ru perpendicular to the direction of the waves, and heat-treated in an oven at 150°C for 30 minutes to form an uneven shape. The tracking performance was observed. The results are shown in Table 4. However, the judgment is based on those that are in close contact with each other without any gaps.
○”, and those with gaps remaining were rated “×”.
第4表
拘束材隘 判定 密着状態
1 0 完全密着
2 0 〃
3 0 〃
4 0 〃
50 ”
6” O斜面部の厚み不均一
7“ 0
8” 0
99 × 角部の隙間が大きい
10° X 制振層と拘束層とが密着せず*は比較
例である。Table 4 Restraint material depth Judgment Adhesion condition 1 0 Complete adhesion 2 0 〃 3 0 〃 4 0 〃 50 ” 6” O Non-uniform thickness of sloped part 7 “ 0 8” 0 99 × Large corner gap 10° The damping layer and the restraining layer did not come into close contact with each other.* is a comparative example.
以上(a) (b) (C)の試験結果から判るとおり
、本発明の拘束材は加工性、シート実用強度、割振特性
、凹凸鋼板面への形状追従性が優れており、車輌用サン
ドイッチ型制振構造の拘束材として優れた機能を保有し
ていることが判る。As can be seen from the test results in (a), (b), and (C) above, the restraint material of the present invention has excellent workability, sheet practical strength, distribution characteristics, and shape followability to the uneven steel plate surface, and is suitable for use in sandwich-type vehicles. It can be seen that it has an excellent function as a restraining material for vibration damping structures.
第1図は拘束材の形状追従試験に用いた凹凸波形状の鋼
板の形状および寸法を示す図で、(a)は平面図、(b
)は側面図である。
特許出願人 日本ゼオン株式会社
同 本田技研工業株式会社
同 ゼオン化成株式会社
(a)(b)
第1図
手続補正書(膀
昭和63年 2月 3日
特許庁長官/J%Jll 杢■ 夫 殿1、 4q
牛のスリR
昭和62年南犠第296091号
2、 発明の名称
車輌用拘束材
3、 補正をする者
羽生との関係 特許W)、
住所 東京都千代田区丸の内二丁目6番1号名称
日本ゼオン株式会社 他2名
4、代理人
5、 補正命令の日付 昭和 年 月
日6、 補正により増加する発明の数
8、 補正の内容 3+賦の通り補正の内容(
特願昭62−296091号)1、明細書第4頁第19
行から同第5頁第5行までの「ダンマル等の・・・・・
・アセチレン樹脂、Jの記載を、下記のとおりに訂正す
る。
記
ロジンのグリセリンエステル、重合ロジン、部分水添ロ
ジン、不均化ロジン、ペンタエリスリトールエステル等
のロジン誘導体、α−ピネン、β−ピネン、ジペンテン
等をカチオン重合して得られるポリテルペン樹脂、テル
ペンフェノール等のテルペン樹脂変性物、ジシクロペン
タジェン樹脂、脂肪族系石油樹脂又はその酸変性物、芳
香族系石油樹脂、脂肪族芳香旅人重合系石油樹脂、アル
キルフェノール樹脂、
2、 明細書第13頁の、第1表の下の「(1)日本ゼ
オン製、フィントンC−20OL、軟化温度101℃」
を、「(1)日本ゼオン製、フィントンC−20OL(
軟化点:101℃、酸価:17■KOH/gの脂肪族系
石油樹脂)」と訂正する。Figure 1 is a diagram showing the shape and dimensions of the uneven corrugated steel plate used in the shape following test of the restraint material, (a) is a plan view, (b)
) is a side view. Patent Applicants Nippon Zeon Co., Ltd. Honda Motor Co., Ltd. Zeon Kasei Co., Ltd. (a) (b) Figure 1 Procedural Amendment (Bulletin February 3, 1988 Commissioner of the Japan Patent Office/J%Jll Moku ■ Husband) 1, 4q
Cow Pickpocket R Minamisai No. 296091 of 1988 2, Name of the invention: Vehicle restraint material 3, Relationship with Amendator Hanyu Patent W), Address: 2-6-1 Marunouchi, Chiyoda-ku, Tokyo Name
Zeon Co., Ltd. and 2 others 4, agent 5, date of amendment order 6, Showa year, month, day 6, number of inventions increased by amendment 8, content of amendment 3 + content of amendment as per installment (
Patent Application No. 62-296091) 1, Specification page 4, No. 19
From line 5 to line 5 on page 5 of the same page, ``Dammar etc...''
- The description of acetylene resin, J, is corrected as follows. Glycerin ester of rosin, polymerized rosin, partially hydrogenated rosin, disproportionated rosin, rosin derivatives such as pentaerythritol ester, polyterpene resin obtained by cationic polymerization of α-pinene, β-pinene, dipentene, etc., terpene phenol, etc. Terpene resin modified product, dicyclopentadiene resin, aliphatic petroleum resin or its acid modified product, aromatic petroleum resin, aliphatic aromatic polymeric petroleum resin, alkylphenol resin, 2. On page 13 of the specification, "(1) Nippon Zeon, Finton C-20OL, softening temperature 101℃" under Table 1
``(1) Finton C-20OL manufactured by Nippon Zeon (
Softening point: 101℃, acid value: 17■KOH/g aliphatic petroleum resin)'' is corrected.
Claims (1)
れる拘束材であって、粘着付与樹脂100重量部に対し
てエチレン系樹脂3〜100重量部およびガラス繊維3
〜75重量部を少くとも配合してなる組成物で形成され
たことを特徴とする車輌用拘束材。A restraining material that is laminated by sandwiching a damping material on a vibration base material in a vehicle, etc., which contains 3 to 100 parts by weight of ethylene resin and 3 parts by weight of glass fiber per 100 parts by weight of tackifying resin.
A restraining material for a vehicle, characterized in that it is formed from a composition containing at least 75 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29609187A JPH01141143A (en) | 1987-11-26 | 1987-11-26 | Constrained material for vehicle |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29609187A JPH01141143A (en) | 1987-11-26 | 1987-11-26 | Constrained material for vehicle |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01141143A true JPH01141143A (en) | 1989-06-02 |
Family
ID=17829005
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29609187A Pending JPH01141143A (en) | 1987-11-26 | 1987-11-26 | Constrained material for vehicle |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01141143A (en) |
-
1987
- 1987-11-26 JP JP29609187A patent/JPH01141143A/en active Pending
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