JP2836068B2 - Damper - Google Patents
DamperInfo
- Publication number
- JP2836068B2 JP2836068B2 JP62157189A JP15718987A JP2836068B2 JP 2836068 B2 JP2836068 B2 JP 2836068B2 JP 62157189 A JP62157189 A JP 62157189A JP 15718987 A JP15718987 A JP 15718987A JP 2836068 B2 JP2836068 B2 JP 2836068B2
- Authority
- JP
- Japan
- Prior art keywords
- damper
- rubber
- viscoelastic body
- present
- viscoelastic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000003860 storage Methods 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 description 36
- 239000005060 rubber Substances 0.000 description 35
- 239000000463 material Substances 0.000 description 18
- 239000000835 fiber Substances 0.000 description 16
- -1 lead and others Chemical class 0.000 description 16
- 230000000694 effects Effects 0.000 description 13
- 239000000314 lubricant Substances 0.000 description 11
- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- 238000002955 isolation Methods 0.000 description 9
- 229920003023 plastic Polymers 0.000 description 9
- 239000004033 plastic Substances 0.000 description 9
- 238000013016 damping Methods 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 239000004014 plasticizer Substances 0.000 description 7
- 239000000945 filler Substances 0.000 description 6
- 239000003190 viscoelastic substance Substances 0.000 description 6
- 238000013329 compounding Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000002759 woven fabric Substances 0.000 description 5
- 229920000459 Nitrile rubber Polymers 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004636 vulcanized rubber Substances 0.000 description 4
- 239000005062 Polybutadiene Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
- 229920001084 poly(chloroprene) Polymers 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Chemical class C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-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
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Chemical class 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 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229920003049 isoprene rubber Polymers 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Chemical class OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920000572 Nylon 6/12 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006235 chlorinated polyethylene elastomer Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 230000005489 elastic deformation Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920006229 ethylene acrylic elastomer Polymers 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 229920005555 halobutyl Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920005594 polymer fiber Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Vibration Prevention Devices (AREA)
- Laminated Bodies (AREA)
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は機器や構造物等の被加震体に取り付けられ、
これらの被加震体に伝達される振動もしくは震動(以
下、振動と略)エネルギーを吸収するダンパー(減衰装
置)に係り、特に未加硫ゴム等の粘性ないし可塑的性質
をダンピング効果として利用することを特徴とするダン
パーに関する。
[従来の技術]
機器や構造物等に加わる地震等による振動を減少させ
るものとして、ダンパーが従来より知られている。ダン
パーは、それを構成する素材のエネルギー吸収能力を利
用して、振動エネルギーを吸収するものであって、鉛等
の金属、その他に現れる塑性効果を利用したものと、オ
イル等の粘性効果を利用したものとに大別される。
[発明が解決しようとする問題点]
塑性効果を利用したダンパーでは、その変形が小さい
領域では、弾性変形となるため、ダンピング効果が殆ど
現れないという問題がある。
一方、オイル等の粘性効果を利用したダンパーでは、
大きなダンピング効果を得るためには、装置を大型化せ
ざるを得ず、その上、オイルの取扱いや、製品としての
成型加工が難しいなどの問題点がある。しかも、長期使
用時の繊維、保全のための作業が煩雑で、保守管理が容
易ではないという欠点もある。
本発明は、上記従来の問題点を解決し、
できるだけ大きな粘性効果を保つ材料で構成され
その材料の粘性効果(ダンピング効果)を最大限に
発現させる構造であって、
成型加工が簡単
取扱いが簡単
このため、大幅なコストダウンが図れる
という理想的なダンパーを提供することを目的とするも
のである。
[問題点を解決するための手段]
本発明のダンパーは、機器、構造物等の被加震体に取
り付けられ、地震などによる振動を減衰させるためのダ
ンパーであって、網状構造体、波状構造体、ハニカム状
構造体及び織物の少なくとも一つの骨格体と粘弾性体と
を両者が接触した状態で複合させてなり、該粘弾性体の
25℃における50%引張変形時のヒステリシス比h50が0.2
以上であり、かつ、該粘弾性体の、周波数5Hz、歪0.01
%、温度25℃で動的に測定された貯蔵弾性率(E)が、
1(kg/cm2)≦E≦2×104(kg/cm2)であることを特
徴とする。
「作用」
本発明者らは、従来のダンパーの欠点を解消し、前記
〜の特性を備えた理想的な粘性ダンパーについて鋭
意研究を重ねて結果、良好なダンピング効果を得るに
は、繰り返し耐久性、製造コスト、メンテナンス等を総
合的に検討すれば、粘稠性のある粘弾性材料の高減衰性
(高ヒステリシスロス性)を利用するのが最良の方法で
あると判断した。
一方、これらの材料と網目構造体を組合せることによ
って、極めて高減衰のダンパーが得られることを見出
し、本発明を完成させた。
即ち、粘稠性の粘弾性材料は、第2図に示すような応
力−歪曲線を示し、小変形に対しては応力を吸収するこ
とができるものの、大変形に対しては剛性が低下して十
分な強度が発現されない。これに対して、網状構造体、
波状構造体、ハニカム状構造体及び織物は、第3図に示
すような応力−歪曲線を示し、大変形において大きな剛
性を発現することができる。
従って、本発明の如く、これらを複合させることによ
り、小変形から大変形に到る広範な領域で、必要な剛性
を保持しかつ極めて高ロス性でダンピング効果の高いダ
ンパーが提供されるのである。
なお、本発明のダンパーにおいては、骨格体が最も変
形し易い方向が水平方向となるようにするのが好まし
い。例えば網状構造体よりなる骨格体においては、網目
の一本の対角線方向が水平となるように設けるのが好ま
しい。
[実施例]
以下、本発明の実施例について説明する。
本発明のダンパーは、網状構造体、波状構造体、ハニ
カム状構造体及び織物の少なくとも一つの骨格体と粘弾
性体とを両者が接触した状態で複合させてなるものであ
る。
本発明のダンパーの具体的な構成としては、例えば次
のようにして作製されるものが挙げられる。
I 骨格体と粘弾性体とを加圧一体化する。
II 骨格体と粘弾性体とを交互に重ねる。
III 骨格体と粘弾性体とを加圧一体化したものを、骨
格体及び/又は粘弾性体と交互に重ねる。
IV 上記I〜IIIで作製されるものに、更に板状材又は
線状材を積層するなどして組み合せる。
勿論、本発明のダンパーは、その要旨を超えない範囲
で、上記I〜IVの構成に限定されるものではないことは
言うまでもない。
本発明のダンパーで用いられる骨格体は、網状構造
体、波状構造体、ハニカム状構造体及び織物(例えばス
トッキング状のもの)のいずれか一つである。これらの
骨格体の材質としては、特に制限はないが、金属、セラ
ミックス、プラスチックス、FRP、ポリウレタン、綿、
絹等の天然系、ポリアミド、ポリエステル等の合成繊維
が挙げられる。
一方、粘弾性体としては、25℃、50%引張変形時のヒ
ステリシス比(h50)が0.2以上、好ましくは0.3以上の
ものを用いる。なお、引張速度200mm/minで、h50は、第
4図の応力−歪曲線において
の面積比で与えられる。
また、粘弾性体の弾性率は、5Hz、0.01%歪で動的に
測定された貯蔵弾性率Eの25℃における値(E)が、1
≦E≦2×104(Kg/cm2)の範囲、好ましくは5≦E≦
1×104である。
粘弾性材料の引張り破断時における伸びは1%以上あ
ることが好ましく、より好ましくは5%以上、更に好ま
しくは10%以上、特に20%以上あることが好ましい。
このような粘弾性体としては、未加硫ゴム、加硫ゴ
ム、その他前述の特性を有する樹脂、可塑性物質等の中
から上述した特性を有するものが挙げられる。
本発明において、粘弾性体の材料としては、前述のよ
うなヒステリシス比、弾性率特性を有する未加硫ゴム又
は加硫ゴム及びその類似物であることが好ましく、例え
ば、エチレンプロピレンゴム(EPR、EPDM)、ニトリル
ゴム(NBR)、ブチルゴム、ハロゲン化ブチルゴム、ク
ロロプレンゴム(CR)、天然ゴム(NR)、イソプレンゴ
ム(IR)、スチレンブタジエンゴム(SBR)、ブタジエ
ンゴム(BR)、アクリルゴム、エチレン−酢ビゴム(EV
A)、ポリウレタン等の一般ゴム、シリコーンゴム、フ
ッ素ゴム、エチレンアクリルゴム、ポリエステルエラス
トマー、エピクロルヒドリンゴム、塩素化ポリエチレン
等の特殊ゴム、又は熱可塑性エラストマー等が挙げられ
る。なお、粘弾性体が未加硫ゴムの場合には、100℃に
おけるムーニー粘度ML1+4が10以上であることが好まし
い。
これらのゴム材料は単独で用いても、2種以上をブレ
ンドして用いても良い。また、これらのゴム材料には、
各種充填剤、粘着付与剤、滑剤、老化防止剤、可塑剤、
軟化剤、低分子量ポリマー、オイル等、ゴム材料に一般
的な配合剤を混合することにより、目的に応じた硬さ、
ロス特性、耐久性を付与することもできる。特に長期間
に亙り所定の性能を維持するために上記のゴム材料に適
切な老化防止剤、重合禁止剤、スコーチ防止剤等の安定
剤を加えたり、ポリマー自身を水添、その他の変性を行
なうことにより安定化を図ることは極めて有効である。
例えば、骨格体と粘弾性体との接着を行う場合、一般
的には粘弾性体の粘着性を利用した粘着によるのが有利
であるが、この粘着性による接着のために、接着部に必
要な化学結合又は物理結合による網目を導入しても良
い。
本発明の粘弾性体材料としては、上記の物性を有する
未加硫ゴム、加硫ゴムの他に、上記の特性を有する次の
ような物質を利用することもできる。例えば、ポリスチ
レン、ポリエチレン、ポリプロピレン、ABS、ポリ塩化
ビニル、ポリメタクリル酸メチル、ポリカーボネート、
ポリアセタール、ナイロン、塩化ポリエーテル、ポリ四
フッ化エチレン、アセチルセルロース、エチルセルロー
ス等の熱可塑性プラスチック及びこれらのプラスチック
に必要に応じて、次に示す充填剤、可塑剤、軟化剤、粘
着付与剤、オリゴマー滑剤等を配合したものが挙げられ
る。
充填剤: クレー、珪藻土、カーボンブラック、シ
リカ、タルク、硫酸バリウム、炭酸カルシウム、炭酸マ
グネシウム、金属酸化物、マイカ、グラファイト、水酸
化アルミニウム等の鱗片状無機充填剤、各種の金属粉、
木片、ガラス粉、セラミックス粉、粉状ないし粉末ポリ
マー等の粒状ないし粉体状固体充填剤、その他各種の天
然又は人工の短繊維、長繊維(例えば、ワラ、毛、ガラ
スファイバー、金属ファイバー、その他各種のポリマー
ファイバー等)等のゴム用あるいは樹脂用充填剤。
充填剤の配合割合は、ゴム100重量部に対し30〜250重
量部とするのが好ましい。
なお、短繊維としては、ガラス、プラスチック、天然
物等の一般の短繊維が用いられる。例えばこれらの短繊
維には次のような特殊な短繊維補強物も含む。短繊維の
配合状態は、加硫可能なゴムに分子中に
を有する熱可塑性ポリマーの短繊維が、フェノールホル
ムアルデヒド系樹脂の初期縮合物を介してグラフトして
いる強化ゴム組成物のように、短繊維がゴムに化学的に
結合して配合されているものが好ましい。上記熱可塑性
ポリマーの微細な短繊維は、融点が190〜235℃、好まし
くは190〜225℃、特に好ましくは200℃〜220℃である。
ナイロン6、ナイロン610、ナイロン12、ナイロン611、
ナイロン612等のナイロン、ポリヘプタメチレン尿素、
ポリウンデカメチレン尿素等のポリ尿素やポリウレタン
等のポリマー分子中に−CONH−基を有する熱可塑性ポリ
マー、特にはナイロンから形成することが好ましく、平
均系が0.05〜0.8μであり、かつ円形断面を有し、最短
繊維長が好ましくは1μm以上で、繊維軸方向に分子が
配列された微細な短繊維の形態で埋封されていることが
好適である。
軟化剤: アロマティック系、ナフテン系、パラフ
ィン系等の各種ゴム用あるいは樹脂用軟化剤。
軟化剤の好ましく配合割合は、ゴム100重量部に対し
5〜150重量部である。
可塑剤: フタル酸エステル、フタル酸混基エステ
ル、脂肪族二塩基酸エステル、グリコールエステル、脂
肪酸エステル、リン酸エステル、ステアリン酸エステル
等の各種エステル系可塑剤、エポキシ系可塑剤、その他
プラスチック用可塑剤又は、フタレート系、アジペート
系、セバケート系、フォスフェート系、ポリエーテル
系、ポリエステル系等のNBR用可塑剤。
可塑剤の好ましい配合割合は、ゴム100重量部に対し
5〜150重量部である。
粘着付与剤: クマロン樹脂、クマロン−インデン
樹脂、フェノールテルペン樹脂、石油系炭化水素、ロジ
ン誘導体等の各種粘着付与剤(タッキファイヤー)。
粘着付与剤の好ましい配合割合は、ゴム100重量部に
対し1〜50重量部である。
オリゴマー: クラウンエーテル、含フッ素オリゴ
マー、ポリブテン、キシレン樹脂、塩化ゴム、ポリエチ
レンワックス、石油樹脂、ロジンエステルゴム、ポリア
ルキレングリコールジアクリレート、液状ゴム(ポリブ
タジエン、スチレン−ブタジエンゴム、ブタジエン−ア
クリロニトリルゴム、ポリクロロプレン等)、シリコー
ン系オリゴマー、ポリ−α−オレフィン等の各種オリゴ
マー。
オリゴマーの好ましい配合割合は、ゴム100重量部に
対し5〜100重量部である。
滑剤: パラフィン、ワックス等の炭化水素系滑
剤、高級脂肪酸、オキシ脂肪酸等の脂肪酸系滑剤、脂肪
酸アミド、アルキレンビス脂肪酸アミド等の脂肪酸アミ
ド系滑剤、脂肪酸低級アルコールエステル、脂肪酸多価
アルコールエステル、脂肪酸ポリグリコールエステル等
のエステル系滑剤、脂肪アルコール、多価アルコール、
ポリグリコール、ポリグリセロール等のアルコール系滑
剤、金属石鹸、混合系滑剤等の各種滑剤。
滑剤の好ましい配合割合は、ゴム100重量部に対し1
〜50重量部である。
本発明において、粘弾性体材料としては、ビチューメ
ン、粘土等の天然物等を用いることもできる。
本発明のダンパーの使用方法としては、
ダンパーの単独使用
各種免震ゴム(緩衝装置)等の積層ゴムとの併用
等、その他いかなる方法であっても良い。
のダンパーの単独使用の場合、粘弾性体の材料によ
っては復元性が小さく、そのままでは時間と共に流動し
てしまうため、長期間になると形状を保持できなくな
る。このため、この場合には、本発明のダンパーは、粘
弾性体の外表面部を加硫ゴムやこの他の材料で被覆する
ことにより、内部の粘弾性体が外部へ流動するのを防ぐ
と共に、ダンパーが大変形するような使用条件に対して
も、ダンパーの外表面部が十分これに追随できるように
する。この場合、外表面部を構成するもの、例えば、外
容器等は、それ自身十分変形できるものであれば材質等
に制限はない。
の免震ゴム等と併用する場合、ダンパーは免震ゴム
と並列に並べても良いし、第1図に示す如く免震ゴム2
の内部に空洞を設け、その部分に本発明のダンパー1を
挿入し、設置するようにしても良い。第1図の如く、ダ
ンパー1を免震ゴム内に設ける場合には、免震ゴム2の
空洞内壁面がダンパーの被覆層として作用するため、上
述の如く、ダンパーの外表面部を被覆する必要はない
が、免震ゴム等と並列使用する場合には、ダンパーに被
覆層を設けて、あるいは設けずに、ダンパーを固体面と
固体面との間に狭み込んで使用するのが有利である。
(なお、第1図中、3はフランジである。)
このような本発明のダンパーは、各種機器、、構造
物、建物などに適用することにより、振動源から各種機
器、構造物、建築物等に伝達される振動エネルギーを効
率的に吸収し、これを大幅に減衰させることができ、防
振、制振、免震に、また防舷材としても極めて有効であ
る。
[発明の効果]
以上詳述した通り、本発明のダンパーは、網状構造
体、波状構造体、ハニカム状構造体及び織物の少なくと
も一つの骨格体と特定のヒステリシス比を有する粘弾性
体とを両者が接触した状態で複合してなるものであっ
て、骨格体の大変形に対する優れた合成と、粘弾性体の
小変形に対する優れた剛性との相乗作用により、小変形
から大変形に到る広範な領域で、極めて優れた剛性及び
高ロス性を発現し、著しく高ダンピング効果を奏するも
のである。
しかも、
成型加工が容易である。
製品の取扱い、施工が簡単である。
メンテナンスが簡単である。
このため、製品のコストダウンが図れる。
減衰効率が高く、装置のコンパクト化が可能であ
る。
等の効果も奏される。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention is mounted on a vibrated body such as equipment or a structure,
The present invention relates to a damper (damping device) that absorbs vibration or vibration (hereinafter abbreviated as vibration) energy transmitted to an object to be vibrated, and particularly utilizes a viscous or plastic property of unvulcanized rubber or the like as a damping effect. A damper characterized by the above-mentioned. [Related Art] A damper has been conventionally known as a device for reducing vibration caused by an earthquake or the like applied to a device or a structure. The damper absorbs vibration energy by using the energy absorption capacity of the material that composes it.It uses the plastic effect that appears in metals such as lead and others, and uses the viscous effect of oil and the like. Are roughly divided into [Problems to be Solved by the Invention] The damper using the plastic effect has a problem that the damping effect hardly appears because the elastic deformation occurs in a region where the deformation is small. On the other hand, in a damper that uses the viscous effect of oil etc.,
In order to obtain a large damping effect, the size of the apparatus must be increased, and further, there are problems such as difficulty in handling oil and molding as a product. In addition, there is a drawback that the operation for maintenance of the fibers during long-term use is complicated, and the maintenance management is not easy. The present invention solves the above-mentioned conventional problems, and is made of a material that maintains a viscous effect as large as possible and has a structure that maximizes the viscous effect (damping effect) of the material. Therefore, it is an object of the present invention to provide an ideal damper that can significantly reduce costs. [Means for Solving the Problems] The damper of the present invention is a damper that is attached to a vibrated body such as a device or a structure, and attenuates vibration due to an earthquake or the like. Body, at least one skeleton of a honeycomb-like structure and a woven fabric and a viscoelastic body in a state where both are in contact with each other,
50% tensile deformation during hysteresis ratio h 50 of at 25 ° C. 0.2
And the viscoelastic body has a frequency of 5 Hz and a strain of 0.01.
%, The storage modulus (E) dynamically measured at a temperature of 25 ° C.
1 (kg / cm 2 ) ≦ E ≦ 2 × 10 4 (kg / cm 2 ). "Action" The present inventors have solved the drawbacks of the conventional damper, and have conducted intensive studies on an ideal viscous damper having the above-mentioned characteristics. From a comprehensive consideration of manufacturing costs, maintenance, and the like, it was determined that the best method was to use the high damping property (high hysteresis loss property) of a viscous viscoelastic material. On the other hand, it has been found that a damper with extremely high attenuation can be obtained by combining these materials with a network structure, and the present invention has been completed. That is, the viscous viscoelastic material exhibits a stress-strain curve as shown in FIG. 2 and can absorb stress for small deformation, but has reduced rigidity for large deformation. And sufficient strength is not developed. On the other hand, a network structure,
The corrugated structure, the honeycomb-shaped structure, and the woven fabric show a stress-strain curve as shown in FIG. 3, and can exhibit large rigidity in large deformation. Therefore, by combining these as in the present invention, it is possible to provide a damper which maintains the required rigidity, has a very high loss property, and has a high damping effect in a wide range from small deformation to large deformation. . In the damper of the present invention, it is preferable that the direction in which the skeleton is most easily deformed is the horizontal direction. For example, in a skeletal body composed of a net-like structure, it is preferable that one mesh is provided so that the diagonal direction is horizontal. [Example] Hereinafter, an example of the present invention will be described. The damper of the present invention is obtained by combining at least one skeleton of a net-like structure, a wavy structure, a honeycomb-like structure, and a woven fabric with a viscoelastic body in a state where both are in contact with each other. As a specific configuration of the damper of the present invention, for example, a damper manufactured as follows is exemplified. I The skeleton and the viscoelastic body are integrated under pressure. II The skeletal body and the viscoelastic body are alternately stacked. III A skeletal body and a viscoelastic body that are integrated under pressure are alternately stacked with the skeletal body and / or the viscoelastic body. IV A plate-like material or a wire-like material is further combined with the material produced in the above I-III. Of course, it goes without saying that the damper of the present invention is not limited to the configurations I to IV described above without departing from the gist thereof. The skeleton used in the damper of the present invention is any one of a net-like structure, a wavy structure, a honeycomb-like structure, and a woven fabric (for example, a stocking-like one). There is no particular limitation on the material of these skeletons, but metals, ceramics, plastics, FRP, polyurethane, cotton,
Examples include natural fibers such as silk and synthetic fibers such as polyamide and polyester. On the other hand, as the viscoelastic body, one having a hysteresis ratio (h 50 ) at 25 ° C. and 50% tensile deformation of 0.2 or more, preferably 0.3 or more is used. Incidentally, at a tensile speed of 200 mm / min, h 50, the stress of FIG. 4 - in strain curve Given by the area ratio of In addition, the elastic modulus of the viscoelastic body is such that the value (E) at 25 ° C. of the storage elastic modulus E dynamically measured at 5 Hz and 0.01% strain is 1
≦ E ≦ 2 × 10 4 (Kg / cm 2 ), preferably 5 ≦ E ≦
It is 1 × 10 4 . The elongation of the viscoelastic material at the time of tensile break is preferably 1% or more, more preferably 5% or more, further preferably 10% or more, and particularly preferably 20% or more. Examples of such a viscoelastic body include unvulcanized rubber, vulcanized rubber, a resin having the above-mentioned properties, a plastic substance, and the like, which have the above-mentioned properties. In the present invention, as the material of the viscoelastic body, it is preferable that the above-mentioned hysteresis ratio, unvulcanized rubber having elasticity characteristics or vulcanized rubber and the like, for example, ethylene propylene rubber (EPR, EPDM), nitrile rubber (NBR), butyl rubber, halogenated butyl rubber, chloroprene rubber (CR), natural rubber (NR), isoprene rubber (IR), styrene butadiene rubber (SBR), butadiene rubber (BR), acrylic rubber, ethylene -Vinegar rubber (EV
A), general rubber such as polyurethane, silicone rubber, fluorine rubber, ethylene acrylic rubber, polyester elastomer, special rubber such as epichlorohydrin rubber, chlorinated polyethylene, or thermoplastic elastomer. When the viscoelastic body is an unvulcanized rubber, the Mooney viscosity ML 1 + 4 at 100 ° C. is preferably 10 or more. These rubber materials may be used alone or as a blend of two or more. In addition, these rubber materials include
Various fillers, tackifiers, lubricants, anti-aging agents, plasticizers,
By mixing a general compounding agent into a rubber material such as a softening agent, a low molecular weight polymer, an oil, etc., the hardness according to the purpose,
Loss characteristics and durability can also be imparted. Particularly, in order to maintain a predetermined performance over a long period of time, a suitable stabilizer such as an antioxidant, a polymerization inhibitor or an anti-scorch agent is added to the above rubber material, or the polymer itself is hydrogenated or otherwise modified. It is extremely effective to achieve stabilization. For example, when bonding a skeleton body and a viscoelastic body, it is generally advantageous to use adhesion using the tackiness of the viscoelastic body. You may introduce | transduce the network by a natural chemical bond or a physical bond. As the viscoelastic material of the present invention, in addition to the unvulcanized rubber and the vulcanized rubber having the above-mentioned physical properties, the following substances having the above-mentioned properties can be used. For example, polystyrene, polyethylene, polypropylene, ABS, polyvinyl chloride, polymethyl methacrylate, polycarbonate,
Thermoplastics such as polyacetal, nylon, chlorinated polyether, polytetrafluoroethylene, acetylcellulose, ethylcellulose, etc., and if necessary for these plastics, the following fillers, plasticizers, softeners, tackifiers, oligomers Those containing a lubricant or the like are included. Fillers: clay, diatomaceous earth, carbon black, silica, talc, barium sulfate, calcium carbonate, magnesium carbonate, metal oxides, mica, graphite, flaky inorganic fillers such as aluminum hydroxide, various metal powders,
Wood chips, glass powder, ceramic powder, granular or powdered solid fillers such as powdery or powdered polymers, and other various natural or artificial short fibers and long fibers (eg, straw, wool, glass fiber, metal fiber, etc.) Fillers for rubber or resin such as various polymer fibers). The compounding ratio of the filler is preferably 30 to 250 parts by weight based on 100 parts by weight of the rubber. As the short fibers, general short fibers such as glass, plastic, and natural products are used. For example, these short fibers also include the following special short fiber reinforcements. The compounding state of the short fiber is determined by As in the case of a reinforced rubber composition in which short fibers of a thermoplastic polymer having a graft are grafted via an initial condensate of a phenol formaldehyde resin, those in which short fibers are chemically bonded to rubber are compounded. preferable. The fine short fibers of the thermoplastic polymer have a melting point of 190 to 235 ° C, preferably 190 to 225 ° C, particularly preferably 200 to 220 ° C.
Nylon 6, Nylon 610, Nylon 12, Nylon 611,
Nylon such as nylon 612, polyheptamethylene urea,
It is preferable to form a thermoplastic polymer having a -CONH- group in a polymer molecule such as polyurea such as polyundecamethylene urea or polyurethane, particularly nylon, the average system is 0.05 to 0.8 μm, and a circular cross section. It is preferable that the shortest fiber length is preferably 1 μm or more, and it is embedded in the form of fine short fibers in which molecules are arranged in the fiber axis direction. Softeners: Softeners for various rubbers or resins, such as aromatic, naphthenic and paraffinic. The preferred mixing ratio of the softener is 5 to 150 parts by weight based on 100 parts by weight of rubber. Plasticizers: Various ester-based plasticizers such as phthalic acid ester, phthalic acid mixed ester, aliphatic dibasic acid ester, glycol ester, fatty acid ester, phosphate ester, stearic acid ester, epoxy-based plasticizer, and other plastic plastics Or NBR plasticizers such as phthalate, adipate, sebacate, phosphate, polyether and polyester. A preferable mixing ratio of the plasticizer is 5 to 150 parts by weight based on 100 parts by weight of the rubber. Tackifiers: Various tackifiers (tackifiers) such as coumarone resin, coumarone-indene resin, phenol terpene resin, petroleum hydrocarbons, and rosin derivatives. A preferable mixing ratio of the tackifier is 1 to 50 parts by weight based on 100 parts by weight of the rubber. Oligomer: Crown ether, fluorinated oligomer, polybutene, xylene resin, chlorinated rubber, polyethylene wax, petroleum resin, rosin ester rubber, polyalkylene glycol diacrylate, liquid rubber (polybutadiene, styrene-butadiene rubber, butadiene-acrylonitrile rubber, polychloroprene Various oligomers such as silicone-based oligomers and poly-α-olefins. A preferred compounding ratio of the oligomer is 5 to 100 parts by weight based on 100 parts by weight of the rubber. Lubricants: hydrocarbon lubricants such as paraffin and wax, fatty acid lubricants such as higher fatty acids and oxy fatty acids, fatty acid amide lubricants such as fatty acid amides and alkylene bis fatty acid amides, fatty acid lower alcohol esters, fatty acid polyhydric alcohol esters, and fatty acid poly Ester lubricants such as glycol esters, fatty alcohols, polyhydric alcohols,
Various lubricants such as alcohol-based lubricants such as polyglycol and polyglycerol, metal soaps, and mixed lubricants. The preferred compounding ratio of the lubricant is 1 to 100 parts by weight of rubber.
5050 parts by weight. In the present invention, natural materials such as bitumen and clay can be used as the viscoelastic material. As a method of using the damper of the present invention, any other method such as a single use of the damper, a combined use with a laminated rubber such as various seismic isolation rubbers (buffers) and the like may be used. When the damper is used alone, the restoring property is small depending on the material of the viscoelastic body, and the damper flows with time as it is, so that the shape cannot be maintained over a long period of time. For this reason, in this case, the damper of the present invention prevents the internal viscoelastic body from flowing outside by coating the outer surface of the viscoelastic body with vulcanized rubber or another material. In addition, the outer surface of the damper can sufficiently follow the use condition under which the damper is greatly deformed. In this case, the material constituting the outer surface portion, for example, the outer container is not limited as long as it can sufficiently deform itself. When used together with the seismic isolation rubber, etc., the damper may be arranged in parallel with the seismic isolation rubber, or as shown in FIG.
May be provided with a cavity inside, and the damper 1 of the present invention may be inserted into the cavity and installed. As shown in FIG. 1, when the damper 1 is provided in the seismic isolation rubber, since the inner wall surface of the cavity of the seismic isolation rubber 2 acts as a coating layer for the damper, it is necessary to cover the outer surface of the damper as described above. However, when used in parallel with seismic isolation rubber, etc., it is advantageous to use the damper narrowed between solid surfaces, with or without a coating layer on the damper. is there.
(Note that in FIG. 1, reference numeral 3 denotes a flange.) Such a damper of the present invention is applied to various devices, structures, buildings, and the like, so that various devices, structures, and buildings can be used from a vibration source. It can efficiently absorb the vibration energy transmitted to the vehicle, etc., and greatly attenuate it, which is extremely effective for vibration isolation, vibration suppression, seismic isolation, and as a fender. [Effects of the Invention] As described above in detail, the damper of the present invention includes both a viscoelastic body having a specific hysteresis ratio and at least one skeleton body of a network structure, a wavy structure, a honeycomb structure, and a woven fabric. Are in contact with each other, and by the synergistic effect of excellent synthesis for large deformation of skeleton and excellent rigidity for small deformation of viscoelastic body, a wide range from small deformation to large deformation In such a region, extremely excellent rigidity and high loss properties are exhibited, and a remarkably high damping effect is exhibited. In addition, molding is easy. Easy handling and construction of products. Easy maintenance. Therefore, the cost of the product can be reduced. The attenuation efficiency is high and the device can be made compact. And the like.
【図面の簡単な説明】
第1図は本発明のダンパーの使用例を示す縦断面図、第
2図は粘弾性材料の応力−歪曲線、第3図は骨格体の応
力−歪曲線、第4図は材料の応力−歪曲線である。
1……ダンパー、2……免震ゴム。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a longitudinal sectional view showing an example of use of a damper of the present invention, FIG. 2 is a stress-strain curve of a viscoelastic material, FIG. FIG. 4 is a stress-strain curve of the material. 1 ... Damper, 2 ... Seismic isolation rubber.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭62−83139(JP,A) 特開 昭62−74637(JP,A) ────────────────────────────────────────────────── ─── Continuation of front page (56) References JP-A-62-83139 (JP, A) JP-A-62-74637 (JP, A)
Claims (1)
どによる振動を減衰させるためのダンパーであって、網
状構造体、波状構造体、ハニカム状構造体及び織物の少
なくとも一つの骨格体と粘弾性体とを両者が接触した状
態で複合させてなり、該粘弾性体の25℃における50%引
張変形時のヒステリシス比h50が0.2以上であり、かつ、
該粘弾性体の、周波数5Hz、歪0.01%、温度25℃で動的
に測定された貯蔵弾性率(E)が、1(kg/cm2)≦E≦
2×104(kg/cm2)であることを特徴とするダンパー。(57) [Claims] A damper attached to an object to be shaken such as a device or a structure to attenuate vibrations caused by an earthquake or the like. The damper includes at least one skeleton of a net-like structure, a wavy structure, a honeycomb-like structure, and a fabric. The elastic body and the two are combined in a state where they are in contact with each other, the viscoelastic body has a hysteresis ratio h 50 at 50 ° C. at 50% tensile deformation of 0.2 or more, and
The storage elastic modulus (E) of the viscoelastic body dynamically measured at a frequency of 5 Hz, a strain of 0.01% and a temperature of 25 ° C. is 1 (kg / cm 2 ) ≦ E ≦
A damper characterized by 2 × 10 4 (kg / cm 2 ).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62157189A JP2836068B2 (en) | 1987-06-24 | 1987-06-24 | Damper |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62157189A JP2836068B2 (en) | 1987-06-24 | 1987-06-24 | Damper |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63319129A JPS63319129A (en) | 1988-12-27 |
| JP2836068B2 true JP2836068B2 (en) | 1998-12-14 |
Family
ID=15644146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62157189A Expired - Fee Related JP2836068B2 (en) | 1987-06-24 | 1987-06-24 | Damper |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2836068B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002070200A (en) * | 2000-08-30 | 2002-03-08 | Toyo Constr Co Ltd | Vibration control structure for building and construction method therefor |
| CN101896734B (en) * | 2007-10-30 | 2013-01-16 | 株式会社普利司通 | Composition for plug in base-isolated structure, plug for base-isolated structure, and base-isolated structure |
| JP2009108200A (en) * | 2007-10-30 | 2009-05-21 | Bridgestone Corp | Elastomer composition for plug in base isolation structure, composition for plug in base isolation structure, plug in base isolation structure, and base isolation structure |
| JP2011149476A (en) * | 2010-01-20 | 2011-08-04 | Bridgestone Corp | Vibration control damper |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57194506U (en) * | 1981-06-05 | 1982-12-09 | ||
| JPS5950688U (en) * | 1982-09-28 | 1984-04-03 | 昭和電線電纜株式会社 | damping surface plate |
| JPS5958109U (en) * | 1982-10-12 | 1984-04-16 | オ−ツタイヤ株式会社 | Seismic isolation structure |
| JPH0622958B2 (en) * | 1985-04-03 | 1994-03-30 | 株式会社ブリヂストン | Laminated structure |
| JPS6274637A (en) * | 1985-09-30 | 1987-04-06 | マニユフアクツユ−ル・アルサシエン・ド・カウチユ・イスタブリツシユマン・ロラン・エス・ア | Vibration damper |
| JPH0729395B2 (en) * | 1985-10-09 | 1995-04-05 | 株式会社ブリヂストン | Seismic isolation structure |
| JPS6394831A (en) * | 1986-10-09 | 1988-04-25 | 三菱電機株式会社 | Vibration-damping panel |
| JPS63308154A (en) * | 1987-06-10 | 1988-12-15 | ゼオン化成株式会社 | Soundproof floor material |
-
1987
- 1987-06-24 JP JP62157189A patent/JP2836068B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63319129A (en) | 1988-12-27 |
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