JPH0489849A - Vibration-damping and sound-insulating material composition - Google Patents
Vibration-damping and sound-insulating material compositionInfo
- Publication number
- JPH0489849A JPH0489849A JP20553990A JP20553990A JPH0489849A JP H0489849 A JPH0489849 A JP H0489849A JP 20553990 A JP20553990 A JP 20553990A JP 20553990 A JP20553990 A JP 20553990A JP H0489849 A JPH0489849 A JP H0489849A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- sound
- vibration
- parts
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- 238000013016 damping Methods 0.000 title claims abstract description 22
- 239000011810 insulating material Substances 0.000 title claims 2
- 229920001971 elastomer Polymers 0.000 claims abstract description 16
- 239000000853 adhesive Substances 0.000 claims abstract description 8
- 239000000806 elastomer Substances 0.000 claims abstract description 8
- 230000001070 adhesive effect Effects 0.000 claims description 6
- 229920002367 Polyisobutene Polymers 0.000 abstract description 6
- MSFGZHUJTJBYFA-UHFFFAOYSA-M sodium dichloroisocyanurate Chemical compound [Na+].ClN1C(=O)[N-]C(=O)N(Cl)C1=O MSFGZHUJTJBYFA-UHFFFAOYSA-M 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 description 16
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 8
- 238000009413 insulation Methods 0.000 description 8
- 239000005060 rubber Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- -1 liquid paraffin Substances 0.000 description 6
- 238000004898 kneading Methods 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920005549 butyl rubber Polymers 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000010426 asphalt Substances 0.000 description 3
- 239000004566 building material Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000011280 coal tar Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 239000010734 process oil Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- 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 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 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 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 239000004088 foaming agent Substances 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
- 229920005555 halobutyl Polymers 0.000 description 1
- 230000001771 impaired effect Effects 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
- 239000012774 insulation material Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940098695 palmitic acid Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 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
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 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 1
- 229940099259 vaseline Drugs 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Vibration Prevention Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、実用温度領域(−50〜80℃)において、
高いtanδ(損失正接)を有する材料、換言すれば外
部より加えられたエネルギーを吸収してしまう(エネル
ギーロスが大きい)材料を提供するもので、架橋、非架
橋、発泡、非発泡のいずれの形態を問わず、良好な制振
、防振、遮音、吸音、防音、断熱特性を有し、自動車、
内装材、建材、家電機器内装材用途に好適な制振、遮音
材用組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Fields] The present invention is applicable to industrial applications in the practical temperature range (-50 to 80°C).
It provides a material with a high tan δ (loss tangent), in other words, a material that absorbs energy applied from the outside (large energy loss), and can be in any form: crosslinked, non-crosslinked, foamed, or non-foamed It has good vibration damping, anti-vibration, sound insulation, sound absorption, sound insulation, and heat insulation properties regardless of the vehicle,
The present invention relates to a composition for vibration damping and sound insulation materials suitable for interior materials, building materials, and home appliance interior materials.
[従来の技術]
ゴム弾性を有する中〜高反撥ゴム(ブタジェンゴムなど
)系組成物は、本発明組成物に外観、形態を合わせるこ
とが可能であるが、これらは本発明と全く反するエネル
ギーロスの少ない材料で、音、振動を伝搬しやすく、当
該用途には使用できない。[Prior Art] Compositions based on medium to high repulsion rubber (such as butadiene rubber) having rubber elasticity can be made to match the appearance and form of the composition of the present invention, but these compositions cause energy loss, which is completely contrary to the present invention. Due to the small amount of material used, it is easy for sound and vibration to propagate, so it cannot be used for this purpose.
一方、汎用樹脂(PE、PPなど)、高硬度樹脂(PS
、ABS、ナイロンなど)は、本発明の実用温度領域で
はエネルギーロスをほとんど示さず、音、振動を容易に
伝搬し、当該用途には使用できない。On the other hand, general-purpose resins (PE, PP, etc.), high-hardness resins (PS
, ABS, nylon, etc.) exhibit almost no energy loss in the practical temperature range of the present invention, easily propagate sound and vibration, and cannot be used for the purpose concerned.
また、ゴム、プラスチックの中間に位置する熱可塑性エ
ラストマー(ウレタンなど)系組成物の中には、一部エ
ネルギーロスを発現し、僅かではあるが音、振動などを
吸収する材料もあるが、本組成物とは比較にならない低
能力であり、実用性を有さない。Additionally, some thermoplastic elastomer (urethane, etc.) compositions, which are located between rubber and plastic, exhibit some energy loss and absorb sound and vibration, albeit slightly. It has a low ability that is incomparable to other compositions and has no practical use.
[発明が解決しようとする問題点]
本発明者等は、自動車内装材、建材、家電機器内装材用
途に優れた制振、遮音、特性を有する組成物を鋭意検討
した結果、広範囲な温度領域において良好な割振性を有
する制振材組成物を見い圧し、本発明に到達した。[Problems to be Solved by the Invention] As a result of intensive research into compositions that have excellent vibration damping, sound insulation, and properties for use in automobile interior materials, building materials, and home appliance interior materials, the present inventors have found that The present invention was developed based on a search for a damping material composition having good damping properties.
[問題を解決するための手段]
すなわち本発明は、(A)600,000以上の数平均
分子量を有するエラストマーの中から選ばれた少なくと
も一種100重量部に対して、軟化剤(B)1〜200
0重量部、粘着剤(C)1〜2000重量部を配合して
なり、かつ10Hzのtanδ(損失正接)のピーク温
度が一50〜80℃の範囲にあり、そのピーク値が2.
0以上を有することを特徴とする制振、遮音付組成物を
提供するものである。[Means for Solving the Problems] That is, the present invention provides 100 parts by weight of at least one type of elastomer (A) having a number average molecular weight of 600,000 or more, and 1 to 10 parts by weight of the softener (B). 200
0 parts by weight and 1 to 2000 parts by weight of adhesive (C), and the peak temperature of tan δ (loss tangent) at 10 Hz is in the range of 150 to 80°C, and the peak value is 2.
The object of the present invention is to provide a vibration-damping and sound-insulating composition characterized in that it has a coefficient of 0 or more.
本発明に使用される(A)成分としては、例えば天然ゴ
ム、インプレンゴム、高CISブタジェンゴム、アクリ
ルニトリルブタジェンゴム、ブチルゴム、ノルボルネン
ゴム、ポリイソブチレンなどが挙げられる。好ましいエ
ラストマーは、イソプレンゴム、ブチルゴム、ノルボル
ネンゴム、ポリイソブチレンなどであり、特に好ましく
はブチルゴム、ポリイソブチレンである。Examples of the component (A) used in the present invention include natural rubber, imprene rubber, high CIS butadiene rubber, acrylonitrile butadiene rubber, butyl rubber, norbornene rubber, and polyisobutylene. Preferred elastomers include isoprene rubber, butyl rubber, norbornene rubber, and polyisobutylene, with butyl rubber and polyisobutylene being particularly preferred.
(A)成分の数平均分子量は600.000以上、好ま
しくはsoo、ooo以上である。数平均分子量が60
0.000未満の場合には、(B)、(C)成分の抱き
込み性が悪くなる。このため混練り加工性が劣るととも
に、十分な量の(B)、(C)成分を添加できず、制振
、遮音性も悪化する。The number average molecular weight of component (A) is 600.000 or more, preferably soo, ooo or more. Number average molecular weight is 60
If it is less than 0.000, the ability to envelop components (B) and (C) will be poor. For this reason, the kneading processability is poor, and sufficient amounts of components (B) and (C) cannot be added, resulting in poor vibration damping and sound insulation properties.
(B)成分の軟化剤としては、例えばプロセス油、潤滑
油、パラフィン、流動パラフィン、石油アスファルト、
ワセリンなどの石油系軟化剤、コールタール、コールタ
ールピッチなどのコールタール系軟化剤、ヒマシ油、ア
マニ油、ナタネ油、ヤシ油などの脂肪油系軟化剤、トー
ル油、サブ油また蜜ロウ、カルナウバロウ、ラノリンな
どのロウ類、リシノール酸、パルミチン酸、ステアリン
酸、ステアリン酸バイウム、ステアリン酸カルシウム、
ラノリン酸亜鉛などの脂肪酸および脂肪酸塩、石油樹脂
などの合成高分子物質などが挙げられる。これらのうち
、特に好ましいものはナフテニックオイル、アロマティ
ックオイルなどのプロセス油、石油アスファルトである
。Examples of the softening agent (B) include process oil, lubricating oil, paraffin, liquid paraffin, petroleum asphalt,
Petroleum-based softeners such as vaseline, coal tar-based softeners such as coal tar and coal tar pitch, fatty oil-based softeners such as castor oil, linseed oil, rapeseed oil, and coconut oil, tall oil, sub-oil, and beeswax, Carnauba wax, waxes such as lanolin, ricinoleic acid, palmitic acid, stearic acid, baium stearate, calcium stearate,
Examples include fatty acids and fatty acid salts such as zinc lanophosphate, and synthetic polymeric substances such as petroleum resins. Among these, particularly preferred are process oils such as naphthenic oils and aromatic oils, and petroleum asphalt.
(B)成分の軟化剤の配合量は、成分(A)100重量
部に対して1〜2000重量部、好ましくは200〜1
700重量部、さらに好ましくは350〜1500重量
部、特に好ましくは500〜1000重量部である。混
練り加工性の効果を十分得るためには1重量部以上必要
である。2000重量部を超えると、制振、遮音性の低
下とともに組成物の粘度が著しく低下し、加工作業に支
障をきたし好ましくない。The blending amount of the softener (B) is 1 to 2000 parts by weight, preferably 200 to 1 part by weight, per 100 parts by weight of component (A).
The amount is 700 parts by weight, more preferably 350 to 1500 parts by weight, particularly preferably 500 to 1000 parts by weight. In order to sufficiently obtain the effect of kneading processability, 1 part by weight or more is required. If it exceeds 2000 parts by weight, the vibration damping and sound insulation properties will deteriorate and the viscosity of the composition will drop significantly, which will impede processing operations, which is not preferable.
(C)成分の粘着剤としては、ロジン系樹脂、テルペン
系樹脂、テルペン変性系樹脂、脂肪族・芳香族系石油樹
脂、クマロンインデン系樹脂などを挙げることができる
。これらのうち、60℃以上の軟化点を有するものは特
に好ましい。Examples of the adhesive component (C) include rosin resins, terpene resins, terpene modified resins, aliphatic/aromatic petroleum resins, coumaron indene resins, and the like. Among these, those having a softening point of 60° C. or higher are particularly preferred.
(C)成分の粘着剤の配合量は、成分(A)100重量
部に対して1〜2000重量部、好ましくは200〜1
500重量部、さらに好ましくは350〜1200重量
部、特に好ましくは400〜1000重量部である。混
練り加工性の効果を十分得るためには1重量部以上必要
である。2000重量部を超えると粘着性が著しくなり
、加工作業性や後工程作業性が損なわれ好ましくない。The blending amount of the adhesive component (C) is 1 to 2000 parts by weight, preferably 200 to 1 part by weight, per 100 parts by weight of component (A).
The amount is 500 parts by weight, more preferably 350 to 1200 parts by weight, particularly preferably 400 to 1000 parts by weight. In order to sufficiently obtain the effect of kneading processability, 1 part by weight or more is required. If it exceeds 2,000 parts by weight, tackiness becomes significant and processing workability and post-process workability are impaired, which is not preferable.
さらに、本発明の制振材組成物には、上記物質以外に必
要に応じて、炭酸カルシウム、タルク、クレー、シリカ
、マイカ、カーボンブラックなどの無機充填剤、さらに
酸化防止剤、紫外線吸収剤などの安定剤を添加してもよ
い。Furthermore, in addition to the above-mentioned substances, the vibration damping material composition of the present invention may optionally contain inorganic fillers such as calcium carbonate, talc, clay, silica, mica, and carbon black, as well as antioxidants and ultraviolet absorbers. Stabilizers may also be added.
また、本発明の制振材組成物には、制振性能を所定のレ
ベルより低下させない限りにおいて、加硫剤や発泡剤を
添加してもよく、さらには他のエラストマー、例えば乳
化または溶液重合高スチレン(ST50%以上)型スチ
レン−ブタジェン共重合ゴム、クロロプレンゴム、アク
リル系ゴム、ハロゲン化ブチルゴム、スチレン−ブタジ
ェンゴム、エチレン−プロピレン系ゴム、溶液重合スチ
レン−ブタジェンゴム、1.2−ポリブタジェン、芳香
族ビニル化合物−共役ジエンブロック共重合体、エチレ
ン−酢酸ビニル共重合体、ポリブテン1、ポリエチレン
、アタクチックポリプロピレンアイオノマー、スチレン
系樹脂などの一種または二種以上を混合してもよい。Further, the vibration damping material composition of the present invention may contain a vulcanizing agent or a foaming agent, as long as it does not reduce the damping performance below a predetermined level, and may also contain other elastomers, such as emulsified or solution polymerized elastomers. High styrene (ST50% or more) type styrene-butadiene copolymer rubber, chloroprene rubber, acrylic rubber, halogenated butyl rubber, styrene-butadiene rubber, ethylene-propylene rubber, solution polymerized styrene-butadiene rubber, 1,2-polybutadiene, aromatic One or more of vinyl compound-conjugated diene block copolymers, ethylene-vinyl acetate copolymers, polybutene 1, polyethylene, atactic polypropylene ionomers, styrene resins, etc. may be mixed.
また、上記(A)、(B)、(C)の配合組成物は、l
OH2のtanδ(損失正接)のピーク温度が一50〜
80℃、好ましくは0〜70℃、さらに好ましくは10
〜60℃の範囲にあり、かつそのピーク値が2.0以上
、好ましくは、2.5以上、さらに好ましくは3〜7の
ものである。In addition, the blended compositions of (A), (B), and (C) above are l
The peak temperature of tan δ (loss tangent) of OH2 is 150~
80°C, preferably 0 to 70°C, more preferably 10
-60°C, and has a peak value of 2.0 or more, preferably 2.5 or more, and more preferably 3-7.
本発明の制振材組成物の各成分は、熱ロール、加圧式ニ
ーダ−バンバリーミキサ−1押出機、プラネタリ−ミキ
サーなどを用いて加熱下において混合され、またカレン
ダーロールや押出機を用いてンート状に成形したり、射
出成形機で所望の形状に成形することができる。Each component of the damping material composition of the present invention is mixed under heat using a heat roll, a pressure kneader-Banbury mixer-1 extruder, a planetary mixer, etc., and is then mixed using a calender roll or an extruder. It can be molded into a desired shape using an injection molding machine.
[実 施 例]
以下、実施例によって本発明を具体的に説明するが、実
施例によって本発明の範囲が制限されるものではない。[Examples] Hereinafter, the present invention will be specifically explained using Examples, but the scope of the present invention is not limited by the Examples.
なお実施例、比較例において、tanδ(損失正接)は
、動的粘弾性測定装置(PL−DMTA。In Examples and Comparative Examples, tan δ (loss tangent) was measured using a dynamic viscoelasticity measuring device (PL-DMTA).
ポリマーラボラドリース製)を用い、lOH2の周波数
域で一100〜100℃の雰囲気温度下にピーク温度と
ピーク値を測定した。評価は一50〜80°Cのなかに
ピークを有し、かつピーク値が2゜0以上の組成物を[
良:○コと判定、これより外れる組成物を[不良:×コ
と判定した。The peak temperature and peak value were measured at an ambient temperature of -100 to 100[deg.] C. in the 1OH2 frequency range. The evaluation was conducted on compositions that had a peak between -50 and 80°C and a peak value of 2°C or more.
Good: It was judged as ○, and compositions that deviated from this were judged as [Poor: ×].
制振性は、JIS M329−83 5・10防振性
に準拠した。The vibration damping properties were based on JIS M329-83 5.10 vibration damping properties.
すなわち、200X20mmの試験板の上に、170X
20mmの試料シート*1)の縦方向、横方向をそれぞ
れ合わせ、鋼板からなる試験板の一端より30.mmあ
けて乗せて焼付けた後、室温まで放冷したものを試験片
とする。That is, on a 200X20mm test plate, 170X
A 20mm sample sheet*1) was aligned vertically and horizontally, and 30mm was inserted from one end of the test plate made of steel plate. After baking the test pieces after placing them at a distance of 1 mm, the test pieces were left to cool to room temperature.
料)試料シートは、1.5關厚アスファルト制振材/1
a+m厚本発明組成物/2mm厚樹脂系シート(日本合
成ゴム製、特開昭62−288647に準拠)の積層シ
ートとし、0゜8mm鋼板に貼り合わせ焼付けた。Material) The sample sheet is 1.5 thick asphalt vibration damping material/1
A laminated sheet of a+m thick composition of the present invention/2 mm thick resin sheet (manufactured by Japan Synthetic Rubber Co., Ltd., in accordance with JP-A-62-288647) was laminated and baked on a 0°8 mm steel plate.
次に、試料を焼付けていない方の試験板の端を試験器に
しっかり固定し、恒温槽にて40℃に保つ。電磁加振器
に130〜140Hzの電流を流して板を共振させ、次
の振幅が最大となるときの周波数を測定する。次に、そ
の両側で振幅が1/FΣになる点の周波数を測定する。Next, the end of the test plate on which the sample is not baked is firmly fixed in the tester and kept at 40°C in a constant temperature bath. A current of 130 to 140 Hz is applied to the electromagnetic exciter to cause the plate to resonate, and the frequency at which the next amplitude reaches its maximum is measured. Next, the frequency at the point where the amplitude becomes 1/FΣ on both sides is measured.
次の式により防振係数を算出する。Calculate the vibration isolation coefficient using the following formula.
ここに d:防振係数
fo:共振点の周波数Hz
fl、f2:共振点の両側で振幅が共振点のピーク値の
1/、I’Σとなる
周波数Hzf2>fl
(評 価)
0:d=0.4以上
△:d=0.4〜0.3
X:d=0.3未満
混練加工性は、ロール、バンバリー、ニーター押出機、
プラネタリ−ミキサー混練時のコンパウンドのまとまり
性により評価し、まとまり性良好組成物は[◎コ、やや
良好は[○コ、不良は[×]とした。Here, d: Anti-vibration coefficient fo: Frequency at the resonance point Hz fl, f2: Frequency at which the amplitude on both sides of the resonance point is 1/I'Σ of the peak value at the resonance point Hzf2>fl (Evaluation) 0: d = 0.4 or more △: d = 0.4 to 0.3
The cohesiveness of the compound during kneading with a planetary mixer was evaluated, and compositions with good cohesiveness were rated as ``◎'', those that were somewhat good were rated as [○], and those that were poor were rated as [x].
実施例1.2.5.6
(A)成分のブチルゴム、ポリイソブチレン(ビスタネ
ックスMML−14Q、エクソン化学製)、(B)成分
のナフテン系オイル、(C)成分のクリアロン(P−9
0、安原油脂製)、ニスクロン(G−90、新日鉄化学
製)、およびその他の配合剤を表−1に示す配合割合で
5にプラネタリ−ミキサーにより混練し、プレス機によ
り所定厚さに調整し、サンプルを得た。そのテスト結果
を表−1に示した。Example 1.2.5.6 (A) component butyl rubber, polyisobutylene (Vistanex MML-14Q, manufactured by Exxon Chemical), (B) component naphthenic oil, (C) component Clearon (P-9)
0, cheap crude oil), Niscrone (G-90, made by Nippon Steel Chemical Co., Ltd.), and other compounding agents were kneaded into 5 using a planetary mixer in the proportions shown in Table 1, and the mixture was adjusted to a predetermined thickness using a press. , obtained the sample. The test results are shown in Table-1.
実施例3.4
(A)成分のポリイソブチレン(ビスタネックスMML
−14Q、エクソン化学製)、ノルボルネンゴム(NS
X2OB、日本ゼオン製)、(B)成分のナフテン系オ
イル、(C)成分のクリアロン(P−90、安原油脂製
)、およびその他の配合剤を表−1に示す配合割合で3
℃ニーダ−により混練し、プレス機により所定厚さに調
整し、サンプルを得た。そのテスト結果を表−1に示し
た。Example 3.4 Component (A) polyisobutylene (Vistanex MML
-14Q, manufactured by Exxon Chemical), norbornene rubber (NS
X2OB, manufactured by Nippon Zeon), (B) component naphthenic oil, (C) component Clearon (P-90, manufactured by Yasushi Oil), and other compounding agents in the proportions shown in Table 1.
The mixture was kneaded using a °C kneader and adjusted to a predetermined thickness using a press to obtain a sample. The test results are shown in Table-1.
比較例1〜6
各成分の種類、量などを変化させた以外は実施例1と同
様にした。結果を表−2に示す。Comparative Examples 1 to 6 Comparative Examples 1 to 6 were carried out in the same manner as in Example 1 except that the types and amounts of each component were changed. The results are shown in Table-2.
比較例1は、粘着剤の量が本特許請求の範囲を超えるも
のであり、tanδピーク値、防振係数において欠点を
有している。In Comparative Example 1, the amount of adhesive exceeds the scope of the claims of the present invention, and it has drawbacks in tan δ peak value and vibration damping coefficient.
比較例2は、軟化剤の量が本特許請求の範囲を超えるも
のであり、ニーダ−およびプラネタリ−ミキサーで加工
できず、均一な組成物が得られなかった。In Comparative Example 2, the amount of softener exceeded the range claimed in the present invention, and therefore it could not be processed using a kneader or a planetary mixer, and a uniform composition could not be obtained.
比較例3は、粘着剤の量が本特許請求の範囲未満のもの
であり、tanδピーク温度が低く、防振係数、混線加
工性に劣ることがわかる。It can be seen that in Comparative Example 3, the amount of adhesive was less than the claimed range of the present invention, the tan δ peak temperature was low, and the vibration damping coefficient and crosstalk processability were poor.
比較例4.5.6は、エラストマーの平均分子量が本特
許請求の範囲未満のものであり、これらはいずれもta
nδピーク値と防振係数を満足していない。In Comparative Examples 4.5.6, the average molecular weight of the elastomer is less than the claimed range of the present invention, and these are all ta
The nδ peak value and vibration damping coefficient are not satisfied.
以上表−1により、実施例は混練加工性、tanδ(損
失正接)のピーク温度およびピーク値のいずれも満足し
、優れた物性を有する組成物であるのに対し、比較例は
いずれかの評価で欠点を有し、満足できるものではない
。As shown in Table 1 above, the composition of the example satisfies both the kneading processability and the peak temperature and peak value of tan δ (loss tangent), and has excellent physical properties, whereas the comparative example is a composition that has excellent physical properties. It has some drawbacks and is not satisfactory.
以下余白
[発明の効果]
本発明の組成物は、実用温度領域(−50〜80℃)に
おいて外部より加えられたエネルギーを吸収する能力に
優れ、架橋、非架橋、発泡、非発泡の形態を問わず、良
好な制振、遮音、吸音、防音、断熱特性を有し、自動車
内装材、建材(床裏打ち、壁、天井材など)、家電、O
A機器内装材など広範な用途にわたって有用でき、産業
上の利用価値は極めて大きい。Margins below [Effects of the Invention] The composition of the present invention has an excellent ability to absorb energy applied from the outside in the practical temperature range (-50 to 80°C), and has crosslinked, non-crosslinked, foamed, and non-foamed forms. It has good vibration damping, sound insulation, sound absorption, soundproofing, and heat insulation properties, and can be used as automobile interior materials, building materials (floor lining, walls, ceiling materials, etc.), home appliances,
A: It can be used in a wide range of applications, such as equipment interior materials, and has extremely high industrial value.
特許出願人 日本合成ゴム株式会社Patent applicant: Japan Synthetic Rubber Co., Ltd.
Claims (1)
ストマーの少なくとも一種100重量部に対して、軟化
剤(B)1〜2000重量部、粘着剤(C)1〜200
0重量部を配合してなり、かつ10Hzのtanδ(損
失正接)のピーク温度が−50〜80℃の範囲にあり、
そのピーク値が2.0以上であることを特徴とする制振
、遮音材組成物。(A) 100 parts by weight of at least one type of elastomer having a number average molecular weight of 600,000 or more, 1 to 2000 parts by weight of the softener (B), and 1 to 200 parts by weight of the adhesive (C).
0 parts by weight, and the peak temperature of tan δ (loss tangent) at 10 Hz is in the range of -50 to 80 °C,
A vibration damping and sound insulating material composition characterized in that its peak value is 2.0 or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20553990A JP2861320B2 (en) | 1990-08-02 | 1990-08-02 | Vibration control and sound insulation composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20553990A JP2861320B2 (en) | 1990-08-02 | 1990-08-02 | Vibration control and sound insulation composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0489849A true JPH0489849A (en) | 1992-03-24 |
JP2861320B2 JP2861320B2 (en) | 1999-02-24 |
Family
ID=16508569
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20553990A Expired - Lifetime JP2861320B2 (en) | 1990-08-02 | 1990-08-02 | Vibration control and sound insulation composition |
Country Status (1)
Country | Link |
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JP (1) | JP2861320B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003060005A1 (en) * | 2001-12-27 | 2003-07-24 | Cci Corporation | Vibration-damping composition and vibration-damping structure |
WO2009087934A1 (en) * | 2008-01-07 | 2009-07-16 | Nitto Denko Corporation | Vibration-damping reinforcing composition, vibration-damping reinforcing member, and vibration-damping reinforcing method for thin plate |
JP2015086344A (en) * | 2013-11-01 | 2015-05-07 | 住友ゴム工業株式会社 | Rubber composition for tire sound absorption member |
WO2018061861A1 (en) * | 2016-09-27 | 2018-04-05 | 株式会社クラレ | Intermediate film for laminated glass |
-
1990
- 1990-08-02 JP JP20553990A patent/JP2861320B2/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003060005A1 (en) * | 2001-12-27 | 2003-07-24 | Cci Corporation | Vibration-damping composition and vibration-damping structure |
WO2009087934A1 (en) * | 2008-01-07 | 2009-07-16 | Nitto Denko Corporation | Vibration-damping reinforcing composition, vibration-damping reinforcing member, and vibration-damping reinforcing method for thin plate |
JP2009161659A (en) * | 2008-01-07 | 2009-07-23 | Nitto Denko Corp | Damping and reinforcing composition, damping and reinforcing material and method for damping and reinforcing thin plate |
US8298673B2 (en) | 2008-01-07 | 2012-10-30 | Nitto Denko Corporation | Vibration-damping reinforcement composition, vibration-damping reinforcement material, and method for vibration damping and reinforcement of thin sheet |
JP2015086344A (en) * | 2013-11-01 | 2015-05-07 | 住友ゴム工業株式会社 | Rubber composition for tire sound absorption member |
WO2018061861A1 (en) * | 2016-09-27 | 2018-04-05 | 株式会社クラレ | Intermediate film for laminated glass |
Also Published As
Publication number | Publication date |
---|---|
JP2861320B2 (en) | 1999-02-24 |
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