JPH02292347A - Vibration-damper composition and vibration-damping laminate - Google Patents
Vibration-damper composition and vibration-damping laminateInfo
- Publication number
- JPH02292347A JPH02292347A JP11223289A JP11223289A JPH02292347A JP H02292347 A JPH02292347 A JP H02292347A JP 11223289 A JP11223289 A JP 11223289A JP 11223289 A JP11223289 A JP 11223289A JP H02292347 A JPH02292347 A JP H02292347A
- Authority
- JP
- Japan
- Prior art keywords
- damping
- vibration
- damping material
- weight
- material composition
- 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.)
- Granted
Links
- 238000013016 damping Methods 0.000 title claims abstract description 103
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 17
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000005977 Ethylene Substances 0.000 claims abstract description 15
- 229920005604 random copolymer Polymers 0.000 claims abstract description 15
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 14
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 5
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 4
- 239000000463 material Substances 0.000 claims description 85
- 229910052751 metal Inorganic materials 0.000 claims description 11
- 239000002184 metal Substances 0.000 claims description 11
- 238000010030 laminating Methods 0.000 claims description 3
- 229920005672 polyolefin resin Polymers 0.000 abstract description 17
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract description 8
- 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 abstract description 8
- 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 abstract description 8
- 239000000758 substrate Substances 0.000 abstract description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 229910052742 iron Inorganic materials 0.000 abstract description 2
- 241000400624 Eucalyptus punctata Species 0.000 abstract 1
- 238000002425 crystallisation Methods 0.000 abstract 1
- 230000008025 crystallization Effects 0.000 abstract 1
- -1 cyclic olefin Chemical class 0.000 description 9
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000010960 cold rolled steel Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 4
- 239000012943 hotmelt Substances 0.000 description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- HLWRUJAIJJEZDL-UHFFFAOYSA-M sodium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate Chemical compound [Na+].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC([O-])=O HLWRUJAIJJEZDL-UHFFFAOYSA-M 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- WWUVJRULCWHUSA-UHFFFAOYSA-N 2-methyl-1-pentene Chemical compound CCCC(C)=C WWUVJRULCWHUSA-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
- 229910000906 Bronze Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 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
- 239000010974 bronze Substances 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- KNDQHSIWLOJIGP-UMRXKNAASA-N (3ar,4s,7r,7as)-rel-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1,3-dione Chemical compound O=C1OC(=O)[C@@H]2[C@H]1[C@]1([H])C=C[C@@]2([H])C1 KNDQHSIWLOJIGP-UMRXKNAASA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- MNUHUVIZSPCLFF-UHFFFAOYSA-N 1-methylhept-6-ene-1,2,4,5-tetracarboxylic acid Chemical compound OC(=O)C(C)C(C(O)=O)CC(C(O)=O)C(C=C)C(O)=O MNUHUVIZSPCLFF-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
- 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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 1
- 125000004810 2-methylpropylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:2])C([H])([H])[*:1] 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- TWCRBBJSQAZZQB-UHFFFAOYSA-N 3-methylidenehexane Chemical compound CCCC(=C)CC TWCRBBJSQAZZQB-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- RYKZRKKEYSRDNF-UHFFFAOYSA-N 3-methylidenepentane Chemical compound CCC(=C)CC RYKZRKKEYSRDNF-UHFFFAOYSA-N 0.000 description 1
- LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 1
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- SUWJESCICIOQHO-UHFFFAOYSA-N 4-methylhex-1-ene Chemical compound CCC(C)CC=C SUWJESCICIOQHO-UHFFFAOYSA-N 0.000 description 1
- OEMSKMUAMXLNKL-UHFFFAOYSA-N 5-methyl-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C)=CCC2C(=O)OC(=O)C12 OEMSKMUAMXLNKL-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920002430 Fibre-reinforced plastic Polymers 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-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
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 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
- NFRQMYYLARDEQA-UHFFFAOYSA-N [cyclohexyl(dimethoxy)silyl]oxymethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCO[Si](OC)(OC)C1CCCCC1 NFRQMYYLARDEQA-UHFFFAOYSA-N 0.000 description 1
- 229920001893 acrylonitrile styrene Polymers 0.000 description 1
- 229920006127 amorphous resin Polymers 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 229920006038 crystalline resin Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011151 fibre-reinforced plastic Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 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
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 238000009774 resonance method Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- NVAZFWGSXWKRIF-UHFFFAOYSA-N triethoxysilyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)OC(=O)C(C)=C NVAZFWGSXWKRIF-UHFFFAOYSA-N 0.000 description 1
- HLOLETUOZGAKMT-UHFFFAOYSA-N trimethoxysilyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)OC(=O)C(C)=C HLOLETUOZGAKMT-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、非晶質プロピレン・エチレンランダム共重合
体等の非品質ポリオレフィン樹脂、又はこの非品質ポリ
オレフィン樹脂を不飽和カルボン酸等でグラフト変成し
たものを主成分とする制振材組成物に関する.
又、これらの制振材組成物を金属板等の硬質基材と積層
した制振性積層体に関する。Detailed Description of the Invention [Industrial Application Field] The present invention is directed to non-quality polyolefin resins such as amorphous propylene/ethylene random copolymers, or graft modification of these non-quality polyolefin resins with unsaturated carboxylic acids, etc. This invention relates to a damping material composition containing as a main component. The present invention also relates to a damping laminate in which these damping material compositions are laminated with a hard base material such as a metal plate.
近年、生活の高度化に伴い静かな環境への要求が高まっ
ている。このため、冷蔵庫、洗濯機やクーラー等各種家
庭電気機器、OA機器等の事務機器、そして自動車等に
ついて騒音や振動の少ないものが求められている。又、
マンションやオフィスビル等においても、防音性・防振
性が強く求められている。In recent years, as lifestyles have become more sophisticated, the demand for a quiet environment has increased. For this reason, there is a demand for various household electrical appliances such as refrigerators, washing machines, and air conditioners, office equipment such as OA equipment, and automobiles that produce less noise and vibration. or,
There is also a strong demand for soundproofing and vibrationproofing properties in condominiums, office buildings, etc.
従来、家庭電気機器等からの騒音、振動の防止には、制
振材組成物をシート状に成形した制振材と、金属板等の
硬質基材を積層した制振性積層体が、用いられてきた。Conventionally, to prevent noise and vibration from household electrical equipment, etc., a damping material made by forming a damping material composition into a sheet shape and a damping laminate made by laminating a hard base material such as a metal plate have been used. I've been exposed to it.
従来、制振材組成物としては、制振性能を有する樹脂類
、例えば、ポリ酢酸ビニル、ポリ塩化ビニル、酢酸ビニ
ル・マレイン酸ジエステル・共重合体、塩化ビニル・ア
クリル酸エステル共重合体、エチレン・酢酸ビニル共重
合体、アクリロニトリル・スチレン共重合体、軟質系ポ
リオレフィン、合成ゴム、ポリイソブチレン、環状オレ
フィン系炭化水素樹脂等、及びこれらの樹脂類の組成物
等が用いられてきた。Conventionally, damping material compositions include resins with damping properties, such as polyvinyl acetate, polyvinyl chloride, vinyl acetate/maleic acid ester copolymer, vinyl chloride/acrylic acid ester copolymer, and ethylene. - Vinyl acetate copolymers, acrylonitrile-styrene copolymers, soft polyolefins, synthetic rubbers, polyisobutylene, cyclic olefin hydrocarbon resins, etc., and compositions of these resins have been used.
これらの制振材組成物には、加熱、軟化して金属板等の
硬質基材に積層、接着するホットメルトタイプと、溶剤
に溶かして硬質基材に塗布、積層する溶剤タイプとがあ
る。These damping material compositions include hot-melt types, which are heated and softened to be laminated and adhered to hard substrates such as metal plates, and solvent-type compositions, which are dissolved in a solvent and applied to and laminated on hard substrates.
ホットメル1・タイプは溶剤を使用していないため、溶
剤タイプに比べ作業環境や安全性の面で優れている。こ
のため、近年、ホットメルトタイプの方が多く用いられ
るようになってきた。Hot Mel 1 type does not use solvents, so it is superior to solvent types in terms of working environment and safety. For this reason, hot-melt types have come to be used more frequently in recent years.
しかし、ホットメルトタイブの大半は、制振性能が低い
という欠点があった。又、高温での制振性能に優れてい
る制振材組成物であっても、低温から常温にかけての制
振効果に劣っていた。However, most of the hot melt types have a drawback of low vibration damping performance. Further, even if a damping material composition has excellent damping performance at high temperatures, its damping effect from low temperatures to room temperature is poor.
又、ホットメルトタイプに限らず、制振材組成物には結
晶性樹脂が用いられることが多かった。Furthermore, not only the hot melt type, but also crystalline resins have often been used in damping material compositions.
このため、金属板等の硬質基材と積層し冷却する際、制
振材が体積収縮することがある。このため、従来の制振
性積層体においては、制振材に肉痩が生じたり、硬質基
材との接着が不良になったりするという問題点があった
。For this reason, when laminated with a hard base material such as a metal plate and cooled, the damping material may shrink in volume. For this reason, conventional vibration damping laminates have had problems such as thinning of the damping material and poor adhesion to the hard base material.
本発明は、ホットメットタイブの制振材組成物であって
、0〜60゜Cの幅広い温度範囲で良好な制振性能を示
すものを提供することを目的とする。An object of the present invention is to provide a hotmet type damping material composition that exhibits good damping performance over a wide temperature range of 0 to 60°C.
又、制振性積層体を製造する際の制振材の肉痩や硬質基
材との接着不良を解決することを目的とする。Another object of the present invention is to solve the problem of thinning of the damping material and poor adhesion to the hard base material when producing a damping laminate.
(課題解決のための手段〕
本発明は
(1)(a)非品質プロピレン・エチレンランダム共重
合体であって、数平均分子量が1.000〜20,00
0の範囲であり、且つエチレン含有量が8〜30重量%
のもの、及び/又は、
(b)非品質プロピレン・l−プテンランダム共重合体
であって、数平均分子量が1,000〜20,000の
範囲であり、且つ1−ブテン含有量が10〜60重量%
のもの、
からなる、
制振材組成物、及び、
(2)上記の制振材組成物を硬質基材と積層してなる制
振性積層体に関する。(Means for Solving the Problems) The present invention provides (1) (a) a non-quality propylene/ethylene random copolymer having a number average molecular weight of 1.000 to 20,000;
0 and the ethylene content is 8 to 30% by weight
and/or (b) a non-quality propylene/l-butene random copolymer having a number average molecular weight in the range of 1,000 to 20,000 and a 1-butene content in the range of 10 to 20,000. 60% by weight
The present invention relates to a damping material composition comprising the following: and (2) a damping laminate formed by laminating the above vibration damping material composition on a hard base material.
本発明の制振材組成物は、マンションやオフィスビル等
において、床と床の支柱の間に挿入したり、床の下等に
敷いたりして、衝撃音等の騒音や振動を遮断するのに用
いられる。The damping material composition of the present invention can be inserted between floors and floor supports, or placed under floors, etc. in condominiums, office buildings, etc. to block noise and vibration such as impact sounds. used for.
又、シート状或いはブロック状等の制振材として、金属
板等の硬質基材と積層して、制振性積層体とすることも
できる。Further, as a sheet-shaped or block-shaped vibration damping material, it can be laminated with a hard base material such as a metal plate to form a vibration damping laminate.
本発明の制振性積層体の具体的な構成としては、例えば
、次のようなものがある。Specific configurations of the damping laminate of the present invention include, for example, the following.
即ち、
■硬質基材/制振材
■硬質基材/制振材/硬質基材
■硬質基材/制振材/硬質基材/制振材■硬質基材/制
振材/硬質基材/制振材/硬質基材
等がある。That is, ■Hard base material/damping material ■Hard base material/damping material/hard base material ■Hard base material/damping material/hard base material/damping material ■Hard base material/damping material/hard base material /Vibration damping material/Hard base material, etc.
これらの態様のうち、■にしめすものが最も好適に使用
される。Among these embodiments, the one shown in (1) is most preferably used.
本発明の制振材組成物としては、非品質プロとレン・エ
チレンランダム共重合体、非品質ブロピレン・l−ブテ
ンランダム共重合体及びこれらのランダム共重合体の混
練物等の非品質ポリオレフイン樹脂が用いられる。The vibration damping material composition of the present invention includes non-quality polyolefin resins such as non-quality pro and rene/ethylene random copolymers, non-quality propylene/l-butene random copolymers, and kneaded products of these random copolymers. is used.
上記の非品質ポリオレフィン樹脂は、プロピレン含有量
が40重量%以上である。非品質プロピレン・エチレン
共重合体のエチレン含有量は8〜30重量%の範囲であ
る。又、非晶質プロピレンと1−プテン共重合体の1−
ブテン含有量はlO〜60重量%の範囲である。The non-quality polyolefin resin described above has a propylene content of 40% by weight or more. The ethylene content of non-quality propylene-ethylene copolymers ranges from 8 to 30% by weight. In addition, 1- of amorphous propylene and 1-butene copolymer
Butene content ranges from 10 to 60% by weight.
本発明の制振材組成物においては、動的弾性係数E゛が
、O〜60℃の範囲でlxl07〜5×1 0 ” d
yne/cJの範囲であることが、制振性能と形状保持
性との兼ね合いから好ましい。In the damping material composition of the present invention, the dynamic elastic modulus E' is lxl07 to 5x10''d in the range of 0 to 60°C.
The range of yne/cJ is preferable from the viewpoint of a balance between vibration damping performance and shape retention.
従って、非品質ポリオレフィン樹脂が上記の組成であれ
ば、動的弾性係数E′が、0〜60゜Cの範囲で、I
X 1 0’ 〜5 X 1 0’ dyne/ail
の範囲に入るので、制振材組成物として好適である。Therefore, if the non-quality polyolefin resin has the above composition, the dynamic elastic modulus E' is in the range of 0 to 60°C, and the I
X 1 0' ~ 5 X 1 0' dyne/ail
Since it falls within this range, it is suitable as a vibration damping material composition.
非晶質ポリオレフィン樹脂の数平均分子量は1、000
〜20,000の範囲でなくてはならない。The number average molecular weight of amorphous polyolefin resin is 1,000
Must be in the range ~20,000.
数平均分子量が1、000未満であると、常温でも柔ら
かくなり過ぎるので凝集力が弱くなる。If the number average molecular weight is less than 1,000, it becomes too soft even at room temperature, resulting in weak cohesive force.
このため、硬質基材との接着が不良になりやすいという
問題点が生じる。For this reason, a problem arises in that adhesion to the hard base material tends to be poor.
又、数平均分子量が20,000を超えると、非品質ポ
リオレフィン樹脂はゴム状となり、溶融粘度も高くなる
。このため、非晶質ポリオレフィン樹脂を、厚さ0.
5 fi1程度の薄いシートに予め加工たり、硬質基材
上にドクターナイフ等で流延したりすることが困難にな
る.
非品質ポリオレフィン樹脂の結晶化度は20%以下が好
ましく、10%以下であればより好ましい。結晶化度が
20%を超えると、制振性能が低下したり肉痩の問題が
生じたりするので、好ましくない。Furthermore, when the number average molecular weight exceeds 20,000, the non-quality polyolefin resin becomes rubbery and has a high melt viscosity. For this reason, the amorphous polyolefin resin has a thickness of 0.
5 It becomes difficult to process the sheet in advance into a thin sheet of about fi1 or to cast it onto a hard substrate using a doctor knife or the like. The degree of crystallinity of the non-quality polyolefin resin is preferably 20% or less, more preferably 10% or less. If the degree of crystallinity exceeds 20%, it is not preferable because vibration damping performance may deteriorate or a problem of thinning may occur.
非品質ポリオレフィン樹脂には、プロピレン、エチレン
、1−ブテンの他、2−メチルプロピレン、2−メチル
−1−プテン、2−エチル−lプテン、3−メチルーl
−プテン、l−ペンテン、2−メチル−1−ペンテン、
3−メチル−1−ペンテン、4−メチル−1−ペンテン
、2−エチル−1−ペンテン、3−エチル−1−*ンテ
ン、4ーエチル−1−ペンテン、1−ヘキセン、等を共
重合成分として含んでいても良い。In addition to propylene, ethylene, and 1-butene, non-quality polyolefin resins include 2-methylpropylene, 2-methyl-1-butene, 2-ethyl-1-butene, and 3-methyl-1-butene.
-butene, l-pentene, 2-methyl-1-pentene,
3-methyl-1-pentene, 4-methyl-1-pentene, 2-ethyl-1-pentene, 3-ethyl-1-*entene, 4-ethyl-1-pentene, 1-hexene, etc. as copolymerization components. It may be included.
非品質ポリオレフィン樹脂を製造するには、例えば次の
様な重合方法を用いることができる。塩化チタンを塩化
マグネシウムに担持したものとトリアルキルアルミニウ
ムとからなる触媒の存在下、エチレン或いは1−プテン
を、液化プロピレン中に、水素雰囲気下で導入する等の
重合方法で製造できる。In order to produce a non-quality polyolefin resin, the following polymerization method can be used, for example. It can be produced by a polymerization method such as introducing ethylene or 1-butene into liquefied propylene in a hydrogen atmosphere in the presence of a catalyst consisting of titanium chloride supported on magnesium chloride and trialkyl aluminum.
本発明の制振材組成物としては、不飽和カルボン酸及び
/又はその無水物、或いはシラン系カップリング剤でグ
ラフト変成した非品質ポリオレフィン樹脂も用いること
ができる。As the damping material composition of the present invention, a non-quality polyolefin resin graft-modified with an unsaturated carboxylic acid and/or its anhydride or a silane coupling agent can also be used.
不飽和カルボン酸やシラン系カップリング剤とのグラフ
ト変成により、硬質基剤との接着を更に良好にすること
ができる。Graft modification with an unsaturated carboxylic acid or a silane coupling agent can further improve adhesion to a hard base.
非品質ポリオレフィン樹脂のグラフト率は、0.0f〜
10重量%、中でも0.05〜6重量%の範囲が好まし
い。グラフト変成は、不飽和カルボン酸等と、ラジカル
開始剤の存在下で溶融混練する等の方法で行うことがで
きる。The grafting rate of non-quality polyolefin resin is 0.0f~
10% by weight, preferably in the range of 0.05 to 6% by weight. Graft modification can be carried out by a method such as melt-kneading an unsaturated carboxylic acid or the like in the presence of a radical initiator.
不飽和カルボン酸又はその無水物としては、アクリル酸
、メタクリル酸、マレイン酸、イタコン酸、シトラコン
酸、ビシクロ(2.2.1)ヘブトー2−エンー5.6
−ジカルボン酸、無水イタコン酸、無水シトラコン酸、
無水ハイミック酸、ビシクロ(2,2.2)オクター5
−エンー2,3−ジカルボン酸無水物、4−メチルシク
ロヘキサ−4−エンー1.2−ジカルボン酸無水物、■
,2,3,4.5,8,9.10−オクタヒド口ナフタ
レン−2,3−ジカルボン酸無水物、ビシクロ(2,2
.1)オクター7−エンー2.3.5.6−テトラカル
ボン酸−2.3,5.6−ジ無水物、7−オキサビシク
ロ(2,2.1)へブタ−5−エンー2,3−ジカルボ
ン酸無水物等が挙げられる.これらの内で、無水マレイ
ン酸が特に好ましく使用される.
シラン系カップリング剤としては、ビニルトリエトキシ
シラン、メタクリロイルオキシトリメトキシシラン、γ
−メタアクリロイルオキシプロビルトリメトキシシラン
、メタアクリロイルオキシシクロヘキシルトリメトキシ
シラン、T一 タアクリ口イルオキシブロピルトリアセ
チルオキシシラン、メタアクリロイルオキシトリエトキ
シシラン、γ−メタアクリ口イルオキシブ口ビルトリエ
トキシシラン等が挙げられる。Examples of unsaturated carboxylic acids or anhydrides include acrylic acid, methacrylic acid, maleic acid, itaconic acid, citraconic acid, bicyclo(2.2.1) hebuto-2-ene-5.6
- dicarboxylic acid, itaconic anhydride, citraconic anhydride,
Himic anhydride, bicyclo(2,2.2)octa5
-ene-2,3-dicarboxylic anhydride, 4-methylcyclohex-4-ene-1,2-dicarboxylic anhydride, ■
, 2,3,4.5,8,9.10-octahyde-naphthalene-2,3-dicarboxylic anhydride, bicyclo(2,2
.. 1) oct-7-ene-2.3.5.6-tetracarboxylic acid-2.3,5.6-dianhydride, 7-oxabicyclo(2,2.1) to but-5-ene-2,3 - dicarboxylic acid anhydrides, etc. Among these, maleic anhydride is particularly preferably used. Silane coupling agents include vinyltriethoxysilane, methacryloyloxytrimethoxysilane, γ
- methacryloxypropyltrimethoxysilane, methacryloxycyclohexyltrimethoxysilane, T-methacryloyloxypropyltriacetyloxysilane, methacryloxytriethoxysilane, γ-methacryloyloxypropyltriethoxysilane, etc. Can be mentioned.
本発明の制振材組成物としては、非晶質ボリオレフィン
樹脂100重量部に対して、粘着性付与剤5〜100重
量部をブレンドしたものも用い得る。As the damping material composition of the present invention, a composition obtained by blending 5 to 100 parts by weight of a tackifier with 100 parts by weight of an amorphous polyolefin resin may also be used.
粘着性付与剤としては、ガム口ジン、ウッド口ジン、ト
ール油等の天然口ジン、重合口ジン、水添ロジン、マレ
イン化口ジン等の合成口ジン、クマロン・インデン樹脂
、テルペン系樹脂、石油樹脂、フェノール樹脂等が用い
られる。Examples of tackifiers include natural rosin such as gum rosin, wood rosin, tall oil, synthetic rosin such as polymerized rosin, hydrogenated rosin, maleated rosin, coumaron/indene resin, terpene resin, Petroleum resin, phenol resin, etc. are used.
更に、炭酸カルシウム、タルク、マイカ、クレ、珪酸、
石膏、石綿、カーボンブラック、カーボン繊維、金属粉
末、金属繊維等の無機充填剤を添加してもよい。Furthermore, calcium carbonate, talc, mica, clay, silicic acid,
Inorganic fillers such as gypsum, asbestos, carbon black, carbon fiber, metal powder, metal fiber, etc. may be added.
本発明の制振性積層体において、硬質基材として用いら
れる金属板の種類は特に制限されないが、鉄、鋼鉄、合
金鋼、高張力鋼、銅、ステンレス鋼、アルミニウム、ア
ルミニウム合金、燐青銅、青銅、真鍮、鉛などの板が特
に好ましい。In the damping laminate of the present invention, the type of metal plate used as the hard base material is not particularly limited, but may include iron, steel, alloy steel, high-strength steel, copper, stainless steel, aluminum, aluminum alloy, phosphor bronze, Plates of bronze, brass, lead, etc. are particularly preferred.
硬質基材としては、金属板の他、硬質のプラスチックや
繊維強化プラスチックの板やブロック、パーチクルボー
ドや一般の木材、スレート板、セメント板や煉瓦等の無
機材料等も用いることができる。As the hard base material, in addition to metal plates, inorganic materials such as hard plastic or fiber-reinforced plastic plates or blocks, particle boards, general wood, slate boards, cement boards, and bricks can also be used.
又、上記組成物と積層する制振材は、シート状或いはブ
ロック状等の形状の制振材組成物が好ましい。しかし、
制振材組成物を予めシート状或いはブロック状等の形状
に成形したものだけでなく前記制振材組成物を溶融し、
硬質基材の間に流し込んだものであってもよい。Further, the damping material to be laminated with the above composition is preferably a damping material composition in the form of a sheet or a block. but,
In addition to forming the damping material composition into a shape such as a sheet or block in advance, it is also possible to melt the damping material composition,
It may also be poured between hard base materials.
従って、本発明の制振性積層体は、例えば次のようにし
て製造することができる。Therefore, the damping laminate of the present invention can be manufactured, for example, as follows.
上記の制振性組成物を加熱、溶融し、硬質基材の上に流
延し、制振材に成形する。この上から他の硬質基材を重
ね、加熱、圧着するという方法等が可能である。又、上
記の制振材組成物を予め厚さ0.5M程度のシート状の
制振材に加工し、このさ0. 5 mm程度のシート状
の制振材に加工し、この制振材を硬質基材の間に挟んで
加熱、圧着する方法でも製造できる。The above vibration damping composition is heated, melted, and cast onto a hard base material to form a vibration damping material. It is possible to stack another hard base material on top of this, heat it, and press it. Further, the above vibration damping material composition is processed in advance into a sheet-shaped damping material with a thickness of about 0.5M, and this thickness is 0.5M. It can also be manufactured by processing the damping material into a sheet of about 5 mm, sandwiching the damping material between hard base materials, heating and pressing the damping material.
以下に本発明の実施例を示す。 Examples of the present invention are shown below.
実1貢上
制振材組成物として、非晶質プロピレン・エチレンラン
ダム共重合体(Rexene社製、RextacB2A
80、数平均分子tl!7,400(オルトジク口口ベ
ンゼン(ODCB)を溶媒と1, l 3 5°Cで測
定)、エチレン含有量IO重量%)を用いた。この非晶
質プロピレン・エチレン共重合体を加熱、溶融し、ドク
ターナイフを用い一〇、脱脂した冷延鋼板STCC (
厚さ0.5mm,幅20工、長さ270mm)上に流延
し制振材とした。その」二に更に同一の冷延鋼板STC
Cを積層し、160゜C、5 kg/cd、1分の条件
で熱接着して、冷延鋼板/制振材,/冷延鋼板−0.
5 InIII/ O. 2 mffi/ 0. 5
mmの厚さの制振性積層体を作製した。As a vibration damping material composition, an amorphous propylene/ethylene random copolymer (manufactured by Rexene, RextacB2A) was used.
80, number average molecule tl! 7,400 (measured with orthodic benzene (ODCB) as a solvent at 1,135°C, ethylene content IO weight %) was used. This amorphous propylene-ethylene copolymer was heated, melted, and degreased using a doctor knife to produce a cold rolled steel sheet STCC
A vibration damping material was obtained by casting on a material having a thickness of 0.5 mm, a width of 20 mm, and a length of 270 mm. Secondly, the same cold rolled steel sheet STC
C was laminated and thermally bonded under the conditions of 160°C, 5 kg/cd, and 1 minute to form cold rolled steel plate/damping material,/cold rolled steel plate-0.
5 InIII/O. 2mffi/0. 5
A damping laminate having a thickness of mm was produced.
制振性積層体の制振性能は、機械インピーダンスの共振
法で、温度を変えながら損失係数ηを測定することによ
り評価した。測定装置にはブリューエルケアー社製スペ
クトラムアナライザータイプ2032を使用した。測定
温度範囲は0〜90℃とした。データは500Hzでの
値を示す。The damping performance of the damping laminate was evaluated by measuring the loss coefficient η while changing the temperature using a mechanical impedance resonance method. A spectrum analyzer type 2032 manufactured by Brüelkjær was used as the measuring device. The measurement temperature range was 0 to 90°C. Data are shown at 500Hz.
又、制振材組成物の動的粘弾性係数E゛は、東洋ボール
ドウィン社製レオバイブロンMode 1−II Cで
測定した。Further, the dynamic viscoelastic coefficient E' of the damping material composition was measured using a Rheoviblon Mode 1-II C manufactured by Toyo Baldwin.
結果を、第1表及び第1図に示す。The results are shown in Table 1 and FIG.
〔実施例2〕
制振材組成物に、RextacB5A80 (Rexe
ne社製、非晶質プロピレン・エチレンランダム共重合
体、数平均分子量7,300(測定法及び測定条件は実
施例1に同じ)、エチレン含有量20重量%)を用いた
他は、実施例1と同様にして制振性積層体を作製し、損
失係数η及び制振材組成物の動的粘弾性係数E゜を測定
した。[Example 2] RextacB5A80 (Rexe
Example except that an amorphous propylene/ethylene random copolymer manufactured by Ne, Inc., number average molecular weight 7,300 (measurement method and measurement conditions are the same as in Example 1), ethylene content 20% by weight) was used. A damping laminate was prepared in the same manner as in Example 1, and the loss coefficient η and the dynamic viscoelastic coefficient E° of the damping material composition were measured.
結果を、第1表及び第1図に示す。The results are shown in Table 1 and FIG.
〔実施例3〕
制振材組成物として、非晶質プロピレン・1ブテンラン
ダム共重合体(Rexene社製、RextacE5、
数平均分子量9,000(測定法及び測定条件は実施例
1に同じ)、■−ブテン含有量40重量%)を用いた他
は、実施例lと同様にして制振性積層体を作成し、損失
係数η及び制振材組成物の動的粘弾性係数E′を測定し
た。[Example 3] As a damping material composition, amorphous propylene/1-butene random copolymer (manufactured by Rexene, Rextac E5,
A damping laminate was prepared in the same manner as in Example 1, except that the number average molecular weight was 9,000 (the measurement method and conditions were the same as in Example 1), and the -butene content was 40% by weight. , loss coefficient η, and dynamic viscoelastic coefficient E' of the damping material composition were measured.
結果を、第1表及び第1図に示す。The results are shown in Table 1 and FIG.
〔実施例4〕
非品質プロピレン・エチレンランダム共重合体(Rex
ene社製、RextacB2A80)50重量%と、
粘若付与剤(三井石油化学製、ハイレッツTll15)
50重量%を、ブラベンダーで混練しブレンド物を得た
。[Example 4] Non-quality propylene-ethylene random copolymer (Rex
ene, RextacB2A80) 50% by weight,
Viscosity imparting agent (Mitsui Petrochemicals, Highlets Tll15)
50% by weight was kneaded with a Brabender to obtain a blend.
このブレンド物を実施例lと同様に、冷延鋼板上に流延
した。更に別の冷延鋼板を積層し、加熱圧着し、制振性
積層体を作製した。This blend was cast onto a cold rolled steel plate in the same manner as in Example 1. Furthermore, another cold-rolled steel plate was laminated and heat-pressed to produce a vibration-damping laminate.
この制振性積層体の損失係数η、及び制振材組成物の動
的粘弾性係数E゛を実施例1と同様にして測定した。The loss coefficient η of this damping laminate and the dynamic viscoelastic coefficient E′ of the damping material composition were measured in the same manner as in Example 1.
結果を、第1表及び第1図に示す。The results are shown in Table 1 and FIG.
〔実施例5〕
非品質プロピレン・エチレンランダム共重合体(Rex
ene社製、RextacB2A80)100重量部、
無水マレイン酸1重量部、及びラジカル開始剤としてラ
ウロイルパーオキサイド0. 0 0 2重量部を溶融
混練し、無水マレイン酸グラフト共重合物を得た。[Example 5] Non-quality propylene-ethylene random copolymer (Rex
ene, RextacB2A80) 100 parts by weight,
1 part by weight of maleic anhydride and 0.0 parts by weight of lauroyl peroxide as a radical initiator. 0 0 2 parts by weight were melt-kneaded to obtain a maleic anhydride graft copolymer.
この無水マレイン酸グラフト共重合物を制振材に用い、
実施例lと同様にして制振性積層体を作成し、制振性積
層体の損失係数η及び制振材組成物の動的粘弾性係数E
゜を測定した。Using this maleic anhydride graft copolymer as a vibration damping material,
A damping laminate was prepared in the same manner as in Example 1, and the loss coefficient η of the damping laminate and the dynamic viscoelastic coefficient E of the damping material composition were determined.
° was measured.
結果を、第1表に示す。The results are shown in Table 1.
〔比較例1〕
結晶性ボリブロピレン樹脂(宇部興産製ブロックポリプ
ロピレンJ 7 0 1 H)をマレイン化したものを
制振材に用いた他は、実施例lと同様にして制振性積層
体を作成し、損失係数η及び樹脂層の動的粘弾性係数E
゛を測定した。[Comparative Example 1] A damping laminate was prepared in the same manner as in Example 1, except that a maleated crystalline polypropylene resin (Block Polypropylene J 7 0 1 H manufactured by Ube Industries) was used as the damping material. and the loss coefficient η and the dynamic viscoelastic coefficient E of the resin layer
was measured.
結果を、第1表及び第1図に示す。The results are shown in Table 1 and FIG.
実施例1〜5の制振性積層体においては、制振材組成物
の動的粘弾性係数E゛は、0℃では2.1×108〜4
.9X10’の範囲である。又、60℃では、2.3〜
107〜8XlO’の範囲である。In the damping laminates of Examples 1 to 5, the dynamic viscoelastic coefficient E' of the damping material composition was 2.1 x 108 to 4 at 0°C.
.. The range is 9x10'. Also, at 60℃, 2.3~
It is in the range of 107 to 8XlO'.
従って、0℃及び60℃のいづれにおいても、好ましい
動的粘弾性係数の範囲であるIXIO’〜5 X 1
0 9dyne/c/の間に収まっている。Therefore, both at 0°C and 60°C, the dynamic viscoelastic coefficient falls within the preferred range of IXIO' to 5
It falls between 0.9 dyne/c/.
制振性積層体の損失係数ηを本実施例の条件で測定温度
を変化させて測定した場合、η≧0. 1の温度範囲が
、制振性積層体の制振性能が良好な温度範囲である。実
施例1〜5の制振性猜層体においては、この温度範囲も
27〜60℃乃至0℃〜60℃と、室温付近を中心に広
《分布している。When the loss coefficient η of the damping laminate is measured under the conditions of this example while changing the measurement temperature, η≧0. The temperature range No. 1 is the temperature range in which the damping performance of the vibration damping laminate is good. In the damping layer bodies of Examples 1 to 5, this temperature range is also widely distributed around room temperature, from 27 to 60°C to 0°C to 60°C.
このことから、本発明の制振性積層体は、特に室温付近
で優れた制振性能を持つことが判る。This shows that the vibration damping laminate of the present invention has excellent vibration damping performance especially near room temperature.
本発明の制振材組成物は、特定の分子量の非晶質ポリオ
レフィン樹脂或いはその組成物を主成分とする。このた
め、常温付近での制振性能及び形状保持性に優れている
。従って、各種の制振材や遮音材に用いるのに好適であ
る。The damping material composition of the present invention has an amorphous polyolefin resin having a specific molecular weight or a composition thereof as a main component. Therefore, it has excellent vibration damping performance and shape retention near room temperature. Therefore, it is suitable for use in various vibration damping materials and sound insulation materials.
又、この制振材組成物は溶融粘度が低い。従って、加熱
溶融して硬質基村上に流延したり、シート状に成形した
りすることが容易である。Moreover, this damping material composition has a low melt viscosity. Therefore, it is easy to heat and melt it and cast it onto a hard substrate, or to form it into a sheet.
又、この制振材組成物は非晶質の樹脂なので、制振性積
層体材の製造の際、制振材が肉痩したり、金属板との接
着が不良となったりすることがない。In addition, since this damping material composition is an amorphous resin, the damping material will not become thin or have poor adhesion to the metal plate when producing the damping laminate material. .
第1図は、実施例1〜5及び比較例lの制振性積層体の
損失係数ηと温度との関係を示す。
● 実左例1
Φ // 2
温度 (C’)
第1図 損失係数(η)と温度の関係FIG. 1 shows the relationship between the loss coefficient η and temperature of the damping laminates of Examples 1 to 5 and Comparative Example 1. ● Actual left example 1 Φ // 2 Temperature (C') Figure 1 Relationship between loss coefficient (η) and temperature
Claims (6)
合体であって、数平均分子量が1,000〜20,00
0の範囲であり、且つエチレン含有量が8〜30重量%
のもの、及び/又は、 (b)非晶質プロピレン・1−ブテンランダム共重合体
であって、数平均分子量が1,000〜20,000の
範囲であり、且つ1−ブテン含有量が10〜60重量%
のものからなる、 制振材組成物。(1) (a) Amorphous propylene/ethylene random copolymer with a number average molecular weight of 1,000 to 20,00
0 and the ethylene content is 8 to 30% by weight
and/or (b) an amorphous propylene/1-butene random copolymer with a number average molecular weight in the range of 1,000 to 20,000 and a 1-butene content of 10 ~60% by weight
A damping material composition consisting of.
ト変成されている、特許請求の範囲第1項に記載の制振
材組成物。(2) The damping material composition according to claim 1, which is graft-modified with an unsaturated carboxylic acid and/or its anhydride.
る、特許請求の範囲第1項に記載の制振材。(3) The damping material according to claim 1, which is graft-modified with a silane coupling agent.
項に記載の制振材組成物・・・・・100重量部(b)
粘着性付与剤・・・・・・5〜100重量部からなる制
振材組成物。(4) (a) Claim 1, 2, or 3
Damping material composition described in Section 100 parts by weight (b)
A vibration damping material composition comprising 5 to 100 parts by weight of tackifier.
4項に記載の制振材組成物を硬質基材と積層してなる制
振性積層体。(5) A vibration-damping laminate obtained by laminating the damping material composition according to claim 1, 2, 3, or 4 on a hard base material.
記載の制振性積層体。(6) The vibration damping laminate according to claim 5, wherein the hard base material is a metal plate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1112232A JP2583124B2 (en) | 1989-05-02 | 1989-05-02 | Damping material composition and damping laminate using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1112232A JP2583124B2 (en) | 1989-05-02 | 1989-05-02 | Damping material composition and damping laminate using the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02292347A true JPH02292347A (en) | 1990-12-03 |
JP2583124B2 JP2583124B2 (en) | 1997-02-19 |
Family
ID=14581551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1112232A Expired - Fee Related JP2583124B2 (en) | 1989-05-02 | 1989-05-02 | Damping material composition and damping laminate using the same |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998049245A1 (en) * | 1997-04-29 | 1998-11-05 | Dupont Canada Inc. | Moisture resistant coated metal substrates |
JP2007224100A (en) * | 2006-02-22 | 2007-09-06 | Yasuhara Chemical Co Ltd | Hot melt composition and mat and carpet |
CN108219295A (en) * | 2016-12-09 | 2018-06-29 | 富比食品包装有限公司 | Polypropene composition, polypropylene film-making material and its manufacturing method and secondary forming body |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60238343A (en) * | 1984-05-11 | 1985-11-27 | Mitsui Petrochem Ind Ltd | Vibrator damper |
JPS6264844A (en) * | 1985-09-18 | 1987-03-23 | Ube Ind Ltd | Vibration-damping material composition and composite material thereof |
JPS6390550A (en) * | 1986-10-06 | 1988-04-21 | Mitsui Petrochem Ind Ltd | Vibration-damping material |
JPS6479249A (en) * | 1984-08-31 | 1989-03-24 | Ube Industries | Laminate comprising adhesive polyolefin composition and another material |
-
1989
- 1989-05-02 JP JP1112232A patent/JP2583124B2/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60238343A (en) * | 1984-05-11 | 1985-11-27 | Mitsui Petrochem Ind Ltd | Vibrator damper |
JPS6479249A (en) * | 1984-08-31 | 1989-03-24 | Ube Industries | Laminate comprising adhesive polyolefin composition and another material |
JPS6264844A (en) * | 1985-09-18 | 1987-03-23 | Ube Ind Ltd | Vibration-damping material composition and composite material thereof |
JPS6390550A (en) * | 1986-10-06 | 1988-04-21 | Mitsui Petrochem Ind Ltd | Vibration-damping material |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998049245A1 (en) * | 1997-04-29 | 1998-11-05 | Dupont Canada Inc. | Moisture resistant coated metal substrates |
JP2007224100A (en) * | 2006-02-22 | 2007-09-06 | Yasuhara Chemical Co Ltd | Hot melt composition and mat and carpet |
CN108219295A (en) * | 2016-12-09 | 2018-06-29 | 富比食品包装有限公司 | Polypropene composition, polypropylene film-making material and its manufacturing method and secondary forming body |
Also Published As
Publication number | Publication date |
---|---|
JP2583124B2 (en) | 1997-02-19 |
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