JPH0453837A - Fiber-containing rubber sheet - Google Patents
Fiber-containing rubber sheetInfo
- Publication number
- JPH0453837A JPH0453837A JP16145490A JP16145490A JPH0453837A JP H0453837 A JPH0453837 A JP H0453837A JP 16145490 A JP16145490 A JP 16145490A JP 16145490 A JP16145490 A JP 16145490A JP H0453837 A JPH0453837 A JP H0453837A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- fiber
- rubber sheet
- fibers
- sheet
- 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
- 229920001971 elastomer Polymers 0.000 title claims abstract description 133
- 239000005060 rubber Substances 0.000 title claims abstract description 132
- 239000000835 fiber Substances 0.000 title claims abstract description 58
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 18
- 239000007788 liquid Substances 0.000 claims abstract description 18
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 6
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 6
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 6
- 229920006250 telechelic polymer Polymers 0.000 claims abstract description 5
- 239000000463 material Substances 0.000 claims description 52
- 239000003190 viscoelastic substance Substances 0.000 claims description 36
- -1 polyethylene Polymers 0.000 claims description 25
- 239000000047 product Substances 0.000 claims description 23
- 239000004745 nonwoven fabric Substances 0.000 claims description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 17
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical group N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 10
- 239000003063 flame retardant Substances 0.000 claims description 10
- 230000000452 restraining effect Effects 0.000 claims description 10
- 239000004744 fabric Substances 0.000 claims description 8
- 230000005484 gravity Effects 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 7
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 7
- 229920000573 polyethylene Polymers 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 229920005549 butyl rubber Polymers 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- 229910001220 stainless steel Inorganic materials 0.000 claims description 6
- 239000010935 stainless steel Substances 0.000 claims description 6
- 238000005187 foaming Methods 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 229920000459 Nitrile rubber Polymers 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 238000010030 laminating Methods 0.000 claims description 3
- 239000011133 lead Substances 0.000 claims description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 2
- 229920001897 terpolymer Polymers 0.000 claims description 2
- 239000013066 combination product Substances 0.000 claims 1
- 229940127555 combination product Drugs 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 abstract description 20
- 238000013016 damping Methods 0.000 abstract description 18
- 239000000945 filler Substances 0.000 abstract description 10
- 239000002131 composite material Substances 0.000 abstract description 5
- 239000004088 foaming agent Substances 0.000 abstract description 3
- 239000002657 fibrous material Substances 0.000 description 35
- 238000007906 compression Methods 0.000 description 26
- 230000006835 compression Effects 0.000 description 26
- 230000000694 effects Effects 0.000 description 15
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 238000002156 mixing Methods 0.000 description 11
- 239000005062 Polybutadiene Substances 0.000 description 9
- 229920002857 polybutadiene Polymers 0.000 description 9
- 239000010426 asphalt Substances 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 8
- 238000011084 recovery Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 239000006260 foam Substances 0.000 description 6
- 238000009413 insulation Methods 0.000 description 6
- 239000002075 main ingredient Substances 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 description 5
- 239000011491 glass wool Substances 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000006073 displacement reaction Methods 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 239000012774 insulation material Substances 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 239000011120 plywood Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000035939 shock Effects 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- 229920002978 Vinylon Polymers 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920006328 Styrofoam Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 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
- 239000003054 catalyst Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical class C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 150000002366 halogen compounds Chemical class 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 239000002650 laminated plastic Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000010079 rubber tapping Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008261 styrofoam Substances 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 229940006076 viscoelastic substance Drugs 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 241001441571 Hiodontidae Species 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 208000025174 PANDAS Diseases 0.000 description 1
- 208000021155 Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection Diseases 0.000 description 1
- 240000000220 Panda oleosa Species 0.000 description 1
- 235000016496 Panda oleosa Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920006271 aliphatic hydrocarbon resin Chemical class 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 238000009472 formulation Methods 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
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 235000021384 green leafy vegetables Nutrition 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000007542 hardness measurement Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000005923 long-lasting effect 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
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 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
- 239000000025 natural resin Substances 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229940104181 polyflex Drugs 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 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
- 238000012360 testing method Methods 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、振動や衝撃を緩衝する繊維入りゴムシートに
関する。特に振動や衝撃により、緩衝シート自体に強度
を要求される箇所、或いは強い振動が、常時負荷され且
つメンテナンスし難い箇所に適用されるような用途、例
えば、鋭角的な部位を持った機材の保護材、制振を要す
る筐体、ダクト、給排水管の防音被覆材、精密機器の除
振材、音響関連商品の制振材、建築物の床衝撃音遮断材
又は壁面の透過音遮断材、及び建築物の断熱部材、車輌
、船舶の制振部材、NN波防止用制振部材、静電気防止
制振部材、或いは落石防止材等に応用でき、その振動や
衝撃の緩衝、保護を目的とした繊維入りゴムシートに関
する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a fiber-filled rubber sheet that buffers vibrations and shocks. In particular, applications where the shock absorbing sheet itself is required to be strong due to vibrations and shocks, or where it is constantly exposed to strong vibrations and difficult to maintain, such as protection of equipment with sharp edges. materials, housings that require vibration control, ducts, soundproof coating materials for water supply and drainage pipes, vibration isolating materials for precision equipment, damping materials for acoustic-related products, floor impact sound insulation materials for buildings or transmitted sound insulation materials for walls, and Fibers that can be applied to insulation materials for buildings, vibration damping materials for vehicles and ships, vibration damping materials for preventing NN waves, vibration damping materials for preventing static electricity, materials for preventing rockfall, etc., and are used to buffer and protect vibrations and shocks. Regarding rubber sheets.
(従来の技術)
近年、生活水準の向上により住環境、作業環境の改善が
捉唱されており、特に騒音、振動に対して強い排除要求
が生じている。衝撃緩和材としては例えば、発泡スチロ
ール、発泡ウレタン等の発泡体、ダンボール、中空プラ
スチック積層板、及び空気包含プラスチックシート等が
知られている。(Prior Art) In recent years, improvements in living and working environments have been advocated as living standards have improved, and there has been a strong demand for the elimination of noise and vibrations in particular. For example, foams such as styrofoam and urethane foam, cardboard, hollow plastic laminates, and air-containing plastic sheets are known as impact-reducing materials.
また、防振ゴム、無反発ゴム等やオーディオ機器等に用
いられるインシュレーターの如き制振材も使用されてい
る。更に、遮音材として一般に使用されるものにはグラ
スウール、ロックウール等がある。しかし、騒音、振動
に対して比較的寛容であった方面も近年はより高級指向
が強まり、特に設備機器の高精度化に供い極端に振動を
排除しようとする要求や、建築物や車輌、船舶において
はより静かな空間を特徴とする請求が強くなってきた。Also used are vibration damping materials such as anti-vibration rubber, non-repulsion rubber, and insulators used in audio equipment. Further, glass wool, rock wool, etc. are commonly used as sound insulation materials. However, in recent years, even in areas that were relatively tolerant of noise and vibration, there has been a growing trend toward higher quality equipment, and with the increasing precision of equipment, there is a demand for extreme vibration elimination, and buildings, vehicles, There is a growing demand for ships to feature quieter spaces.
これに対する対策として各方面で様々な研究開発が進め
られているが、それを有効に防止する手段に技術的困難
性が伴い、また多額の費用を費やすため、各方面で低コ
ストで騒音・振動を有効に抑制する手段を待ち望んでい
るのが現状である。Various research and developments are being carried out in various fields as countermeasures against this problem, but effective means of preventing it are technically difficult and require a large amount of money. At present, we are waiting for a means to effectively suppress this.
(発明が解決しようとする課題)
しかし、上記発泡スチロール、発泡ウレタン等の発泡体
、ダンボール、中空プラスチック積層板、及び空気包含
プラスチックシート等の衝l!緩和材は小さな応力でも
容易に変形を受け、衝撃を緩和させることが知られてい
るが、これらは復元力、或いは強度が弱い為に一度圧縮
変形を被ると、復元しにくく、破壊し、又比較的小さな
圧力でも、長期に亘ると消耗が大きくなり、元の厚みを
維持できなくなり、相対的にその効果も低下する等の問
題点があり、その結果その機能を消失してしまうと言う
重大な欠点を有していた。(Problems to be Solved by the Invention) However, the above-mentioned foams such as styrofoam and urethane foam, cardboard, hollow plastic laminates, and air-containing plastic sheets are difficult to overcome. It is known that relaxation materials are easily deformed even under small stress and can alleviate the impact, but because they have low restoring force or strength, once they are compressed and deformed, they are difficult to restore, break, or break. Even if the pressure is relatively small, over a long period of time, the wear and tear becomes large, the original thickness cannot be maintained, and the effectiveness is relatively reduced.As a result, the material loses its function, which is a serious problem. It had some drawbacks.
又、防振ゴム、無反発ゴム等は一般に加硫工程を要する
ためにコストが高く、汎用しにくく、比重が大きいため
重量が増大し、更に弾性率が大きく衝撃エネルギーを充
分吸収し得ながった。又オーディオ機器等に用いられる
インシュレーターの如き制振材は、大量の空気を包含す
る必要があるために高さを充分有さなければならず、構
造が複雑となり高価であると言う欠点を有していた。ま
た、グラスウール、ロックウール等の遮音材は、単独で
は形状を維持することが難しく、他の部材、例えば合板
、石膏ボード、鉛板等を用いる必要があり、且つ充分な
効果を発揮させるためには、空気層が必要となっており
、コスト、工数、スペースの各方面で問題となっていた
。In addition, anti-vibration rubber, non-repulsion rubber, etc. generally require a vulcanization process, making them expensive and difficult to use for general purposes.They also have a high specific gravity, which increases their weight, and they also have a large modulus of elasticity, making them difficult to absorb impact energy. It was. In addition, damping materials such as insulators used in audio equipment, etc. must have sufficient height to contain a large amount of air, and have the disadvantage of being complex and expensive. was. In addition, it is difficult for sound insulating materials such as glass wool and rock wool to maintain their shape when used alone, and it is necessary to use other materials such as plywood, gypsum board, lead plates, etc., and in order to achieve sufficient effect. requires an air layer, which poses problems in terms of cost, man-hours, and space.
従って、従来の粘弾性体は、単独で用いた場合はコスト
高となり、汎用衝撃緩衝シートとしては不適当であり、
硬化後の取扱いがゴム粘弾性体であるが故に製造上の制
約が大きく、作業性が悪くなり、設備等を要すると言う
欠点があった。Therefore, when conventional viscoelastic materials are used alone, they are expensive and unsuitable as general-purpose impact cushioning sheets.
Because it is a rubber viscoelastic material that must be handled after curing, there are significant manufacturing restrictions, poor workability, and the disadvantages of requiring equipment.
本発明の目的は、上記の欠点を解決し、低コストで、制
振遮音効果が高く、かつ複合材の強度も大きく、経年に
渡り寸法変化の小さな、制振、遮音効果を維持できる部
材を提供することにある。The purpose of the present invention is to solve the above-mentioned drawbacks, and to provide a member that is low in cost, has a high vibration damping and sound insulation effect, has a high composite material strength, has small dimensional changes over time, and can maintain vibration damping and sound insulation effects. It is about providing.
(課題を解決するための手段)
本発明者等は、上記の目的を達成するため、低コストで
、厚みも薄く、効果的に衝撃エネルギーを吸収し、復元
性が良好で、且つ材料強度も強いために、長期的に効果
を発揮し、作業性も良好である複合部材について鋭意研
究の結果、衝撃エネルギーの吸収に優れた効果を発揮す
るゴム粘弾性体と、復元力及び圧縮強度、引き裂き強度
等の物性に優れた繊維状物を一体型とすることにより、
ゴム粘弾性体単体よりも強度的に大きな効果があるばか
りでなく、衝撃エネルギーの吸収力も増大する相乗効果
を発揮せしめることが可能となる知見を得、本発明を完
成させるに至ったものである。(Means for Solving the Problems) In order to achieve the above object, the present inventors have developed a material that is low cost, has a small thickness, effectively absorbs impact energy, has good restorability, and has high material strength. As a result of extensive research into composite materials that are strong, long-lasting, and workable, we have found that we have developed a rubber viscoelastic material that is highly effective in absorbing impact energy, as well as restoring force, compressive strength, and tear resistance. By integrating a fibrous material with excellent physical properties such as strength,
The present invention was completed based on the knowledge that the rubber viscoelastic material not only has a greater strength effect than the rubber viscoelastic material alone, but also has a synergistic effect that increases the ability to absorb impact energy. .
即ち、本発明は低コストで、制振、遮音効果が高く、か
つ複合材の強度も大きく、経年に渡り寸法変化の小さな
、制振、遮音効果を維持できる部材について繊維状物の
その厚み方向の一部、若しくは全体にゴム粘弾性体を含
浸させることにより、繊維状物の持つ特性とゴム粘弾性
体の持つ特性双方を存し、更に、ゴム帖弾性体単体以上
の優れた衝撃緩衝効果を発揮し、吸音効果も期待でき、
取り扱いが容易で、かつ圧縮特性、復元性に極めて優れ
る繊維入りゴムシートである。本発明の繊維入りゴムシ
ートは、繊維の持つ引張強度と引き裂き強度とゴム粘弾
性体の有する制振性及び圧縮特性を一つの層内で最大限
に利用したものである。That is, the present invention provides a material that is low in cost, has high vibration damping and sound insulation effects, has high composite material strength, has small dimensional changes over time, and can maintain vibration damping and sound insulation effects in the thickness direction of a fibrous material. By impregnating part or all of the rubber viscoelastic material, it has both the characteristics of fibrous material and the characteristics of the rubber viscoelastic material, and also has a shock-absorbing effect superior to that of the rubber elastic material alone. and can also be expected to have a sound absorption effect.
A fiber-containing rubber sheet that is easy to handle and has excellent compression and recovery properties. The fiber-containing rubber sheet of the present invention makes maximum use of the tensile strength and tear strength of the fibers and the vibration damping and compression properties of the rubber viscoelastic body within one layer.
具体的には、本発明の繊維入りゴムシートは、ポリエス
テル、ポリエチレン、ポリプロピレン、アクリル、ビニ
ロン、レーヨン、ナイロン、ポリアミド等の合成繊維、
麻、絹、綿、パーム等の天然繊維、ステンレス、アルミ
ニウム、鉛、鉄等の金属繊維及びグラスウール、グラス
ファイバー、カーボン、セラミック等の無機繊維の一種
、又は併用物に対して、その厚み方向の一部、若しくは
全体にゴム粘弾性体を含浸させるもの、即ち繊維状物の
網目構造内にゴム粘弾性体が入り込んだゴムシートで、
ゴム粘弾性体が、80℃に加温されても形状を保持し、
20℃の条件下で硬度はC型硬度計(日本ゴム協会規格
S RI S−0101)で0〜20を呈するものであ
る。Specifically, the fiber-containing rubber sheet of the present invention includes synthetic fibers such as polyester, polyethylene, polypropylene, acrylic, vinylon, rayon, nylon, and polyamide;
Natural fibers such as linen, silk, cotton, palm, etc., metal fibers such as stainless steel, aluminum, lead, iron, etc., and inorganic fibers such as glass wool, glass fiber, carbon, ceramic, etc., or combinations thereof, in the thickness direction. A rubber sheet partially or entirely impregnated with a rubber viscoelastic material, that is, a rubber sheet in which the rubber viscoelastic material is embedded in a network structure of fibrous materials.
The rubber viscoelastic body retains its shape even when heated to 80°C,
The hardness exhibits a hardness of 0 to 20 on a C-type hardness meter (Japan Rubber Association Standard S RI S-0101) at 20°C.
ゴム粘弾性体は、上記繊維状物の一種又は併用物に対し
て、その厚み方向の一部、或いは全体に含浸し、次いで
発泡硬化せしめられ、その発泡倍率は、1.1〜10倍
である。The rubber viscoelastic material is impregnated into a part or the entire thickness of one of the above fibrous materials or a combination thereof, and then foamed and cured, and the foaming ratio is 1.1 to 10 times. be.
かかるゴム粘弾性体は、分子の両端に反応基を有するテ
レキリツクポリマーを主成分とし、常温で液状である主
剤と、主剤のテレキリツクポリマーと反応し結合し得る
反応基を1分子当たり2個以上有する硬化剤とを主な主
成分とし、5〜80℃の温度域で硬化されて成り、その
性質は難燃性であり、比重は2.3以上である。Such a rubber viscoelastic material is mainly composed of a telechelic polymer having reactive groups at both ends of the molecule, and contains a base material that is liquid at room temperature and a reactive group that can react and bond with the telechelic polymer of the base material per molecule. The main component is a curing agent having two or more of them, and is cured in a temperature range of 5 to 80°C, and has flame retardant properties and a specific gravity of 2.3 or more.
本発明の繊維入りゴムシートは、上記繊維状物の一種又
は併用物に対して、その厚み方向の一部、或いは全体に
ゴム粘弾性体を含浸して得られた複合部材の片面、若し
くは両面にポリエステル、ポリエチレン、塩化ビニル、
エチレン−酢酸ビニルコポリマー(EVA)等のフィル
ム状物、又はこれらの発泡シート状物、クロロブレンゴ
ム(CR)。The fiber-filled rubber sheet of the present invention is a composite member obtained by impregnating one or both of the above fibrous materials with a rubber viscoelastic material into a part or the entire thickness of the fibrous material. polyester, polyethylene, vinyl chloride,
Film-like products such as ethylene-vinyl acetate copolymer (EVA), foamed sheet-like products thereof, and chloroprene rubber (CR).
エチレン−プロピレンターポリマー(EPT)。Ethylene-propylene terpolymer (EPT).
ブチルゴム(IIR)、ニトリルゴム(NR)等のシー
ト状物又はこれらの発泡シート状物、又は不織布、割布
、ガラスクロス、寒冷紗、紙類等のフィルム状物からな
る補強部材の一種又は併用物を積層して形成する。One type or combination of reinforcing members made of sheet materials such as butyl rubber (IIR) and nitrile rubber (NR), or foamed sheet materials thereof, or film materials such as nonwoven fabric, split cloth, glass cloth, cheesecloth, and paper. Formed by laminating.
本発明の繊維入りゴムシートが衝撃緩衝効果に優れるの
は、繊維状物の持つ網目構造にゴム粘弾性物質が入り込
むことにより、ゴム粘弾性物質との接触面積が、平面上
より飛躍的に増大し、これがズリ変形による制振効果の
増大につながり、衝撃エネルギーの吸収性能が増したか
らである。又、圧縮特性においては、繊維状物の網目構
造の中にゴム粘弾性体が入り込むことにより、ゴム粘弾
性体自体の強度を補強することとなり、復元力も増加す
ると考えられる。又コスト面においても、ゴム粘弾性体
を繊維で強化しているため、本発明のシートを加工する
場合には取り扱い作業が非常に容易となり、加工時間、
又は作業時間を短縮する上で非常に効果的であるばかり
でなく、本発明のシートを製造する上においては、長尺
加工が可能であり、コスト的に有利である。又本発明の
施工作業においては被衝撃面に、ゴム粘弾性体自体の粘
着力、或いは接着剤により貼付するだけで、耐衝撃力、
制振性、断熱性等の機能が付与され、しかもゴム粘弾性
体自体の容量も、繊維状物により低減でき、従って低コ
スト化につながるものである。The fiber-filled rubber sheet of the present invention has an excellent shock-absorbing effect because the rubber viscoelastic substance enters the network structure of the fibrous material, so the contact area with the rubber viscoelastic substance is dramatically increased compared to a flat surface. However, this leads to an increase in the damping effect due to shear deformation, and the ability to absorb impact energy increases. In terms of compression properties, it is thought that the penetration of the rubber viscoelastic body into the network structure of the fibrous material reinforces the strength of the rubber viscoelastic body itself, increasing the restoring force. In addition, in terms of cost, since the rubber viscoelastic material is reinforced with fibers, handling work is extremely easy when processing the sheet of the present invention, and processing time and
In addition to being very effective in shortening working time, the sheet of the present invention can be processed into long sheets, which is advantageous in terms of cost. In addition, in the construction work of the present invention, impact resistance,
Functions such as vibration damping and heat insulating properties are imparted, and the capacity of the rubber viscoelastic body itself can be reduced by using the fibrous material, thus leading to cost reduction.
又、ゴム粘弾性体に、難燃剤を配合することにより、本
発明の繊維入りゴムシートに、難燃性の機能付加が可能
であり、或いはゴム粘弾性体に発泡剤を配合することに
より、発泡ゴム粘弾性体に成らしめることが可能であり
、容易に高機能を付加することができる。Furthermore, by blending a flame retardant into the rubber viscoelastic body, it is possible to add a flame retardant function to the fiber-filled rubber sheet of the present invention, or by blending a foaming agent into the rubber viscoelastic body, It can be made into a foamed rubber viscoelastic body, and high functionality can be easily added.
本発明の繊維入りゴムシートの断面構成は、第1図、第
2図に示すように、ポリエステル、ポリエチレン、ポリ
プロピレン、アクリル、ビニロン、レーヨン、ナイロン
、ポリアミド等の合成繊維や麻、絹、綿、パーム等の天
然繊維、ステンレス、アルミニウム、鉛、鉄等の金属繊
維やグラスウール、グラスファイバー、カーボン、セラ
ミック等の無機繊維からなる繊維状物の一種又は併用物
の厚みに対してその厚み方向の一部、若しくは全体に、
ゴム粘弾性体を含浸させ、保護面、或いは振動面に直接
貼り合わせて、この被着面を拘束材として用いるものと
、第3図に示すように、予め拘束材として、ポリエステ
ル、ポリエチレン、塩化ビニル、EVA等のフィルム状
物又はこれらの発泡シート状物、CR,EPT、IIR
等のシート状物又はこれらの発泡シート状物や、不織布
、割布、ガラスクロス、寒冷紗、紙類等のフィルム状物
や、鉄、アルミニウム、鉛、銅、ステンレス等の金属フ
ィルム状物や板状物、合板、単板、コルク、パーティク
ルボード等の木質系拘束材、ホモロメント板、フレキシ
ブルボード、石膏ボード、硅酸カルシウム板、FRP、
セラミックボード等の無機質系拘束材を積層して、保護
面、或いは振動面に貼り合わせて使用するものがあり、
制振特性を上げるためには、第4図に示す如く上下両面
に拘束層を設けることが望ましい。又非常に柔らかい接
触面が要求される場合には、植毛した基材や、ゴムシー
ト等を拘束材としたり、拘束材面に貼り付けてもよい。As shown in FIGS. 1 and 2, the cross-sectional structure of the fiber-filled rubber sheet of the present invention includes synthetic fibers such as polyester, polyethylene, polypropylene, acrylic, vinylon, rayon, nylon, polyamide, hemp, silk, cotton, etc. One type of fibrous material or a combination of fibrous materials, such as natural fibers such as palm, metal fibers such as stainless steel, aluminum, lead, and iron, and inorganic fibers such as glass wool, glass fiber, carbon, and ceramics, in the thickness direction. part or the whole,
There are two types of rubber viscoelastic materials that are impregnated with a rubber viscoelastic material and bonded directly to a protective surface or a vibration surface, and this adhered surface is used as a restraining material. Film-like materials such as vinyl and EVA, or foamed sheet-like materials thereof, CR, EPT, IIR
sheet-like materials such as or foamed sheet-like materials thereof, film-like materials such as non-woven fabric, split cloth, glass cloth, cheesecloth, paper, etc., metal film-like materials and plates such as iron, aluminum, lead, copper, stainless steel, etc. wooden restraining materials such as plywood, veneer, cork, particle board, homoloment board, flexible board, plaster board, calcium silicate board, FRP,
There are products that are used by laminating inorganic restraining materials such as ceramic boards and bonding them to the protective surface or vibration surface.
In order to improve vibration damping characteristics, it is desirable to provide constraining layers on both the upper and lower surfaces as shown in FIG. If a very soft contact surface is required, a flocked base material, a rubber sheet, or the like may be used as the restraining material, or it may be attached to the restraining material surface.
即ち、繊維状物2全体にゴム粘弾性体1が含浸され、被
衝撃面4に貼付された本発明の繊維入りゴムシートの一
例の断面を第1図に、また繊維状物2の一部にゴム粘弾
性体lが含浸され、被衝撃面4に貼付されたものを第2
図に示し、更に繊維状物2の一部にゴム粘弾性体1が含
浸され、拘束材層(ポリエステルフィルム)3を積層し
、被衝撃面4に貼付したものを第3図に、繊維状物20
一部にゴム粘弾性体1が含浸され、その両面に拘束材層
3(有孔鉄板)5が積層され、被衝撃面4に貼付したも
のを第4図に示す。That is, FIG. 1 shows a cross section of an example of a fiber-filled rubber sheet of the present invention in which the entire fibrous material 2 is impregnated with the rubber viscoelastic material 1 and is attached to the impact surface 4, and a portion of the fibrous material 2 is shown in FIG. is impregnated with rubber viscoelastic material l and attached to the impact surface 4.
The fibrous material 2 shown in FIG. thing 20
A part of the rubber viscoelastic body 1 is impregnated, and a restraining material layer 3 (perforated iron plate) 5 is laminated on both sides of the rubber viscoelastic body 1, which is attached to the impact surface 4, as shown in FIG.
ゴム粘弾性体は、ホットメルトタイプ、水系、或いは溶
剤系ディスバージョンタイプ、反応型液状物を硬化反応
せしめて得られるタイプ、油膨潤型ポリマー粉末を可塑
剤中に分散したエラストマーを得るタイプの4つに大別
されるが、本発明を達成する上では、何れのタイプも適
用し得る。それらは、各々個有の特徴を有するが、特に
反応型液状物を硬化反応せしめて得られる架橋粘弾性体
は温度変化による対応も幅広い温度範囲で可能であり、
特に常温反応性を有するポリマーを使用して得られる粘
弾性体は製造工程中で加熱に要するエネルギーや乾燥に
要するエネルギーが不要であるだけでなく、乾燥工程中
で溶剤回収に要する設備が不要であり、水分等による製
造設備の腐食もない点で優れる。There are four types of rubber viscoelastic bodies: hot melt type, water-based or solvent-based dispersion type, type obtained by curing a reactive liquid, and type obtained by obtaining an elastomer by dispersing oil-swellable polymer powder in a plasticizer. However, any type can be applied to achieve the present invention. Each of them has its own unique characteristics, but in particular, crosslinked viscoelastic bodies obtained by curing reactive liquid substances can respond to temperature changes over a wide temperature range.
In particular, viscoelastic bodies obtained using polymers that are reactive at room temperature not only require no energy for heating or drying during the manufacturing process, but also do not require equipment for recovering solvents during the drying process. It is excellent in that there is no corrosion of manufacturing equipment due to moisture, etc.
架橋粘弾性体の中でも次の条件を具備する物質は、本発
明に適用する粘弾性体としては特に望ましいものである
。即ち、本発明で称されるゴム粘弾性体とは、常温で液
状であり、且つ常温で反応した後の硬化物質が、80℃
に加温されても形状を維持し、20℃の条件下で硬度が
、C型硬度計(日本ゴム協会規格S RI S−010
1)で50以下である条件を満足するものである。上記
条件を満足し得る反応性物質としては、例えば第1表に
示す官能基を有する液状ゴムと架橋剤の組合せがある。Among crosslinked viscoelastic bodies, substances that meet the following conditions are particularly desirable as viscoelastic bodies to be applied to the present invention. That is, the rubber viscoelastic material referred to in the present invention is liquid at room temperature, and the cured material after reacting at room temperature is 80°C.
It maintains its shape even when heated to
1) satisfies the condition of 50 or less. Examples of reactive substances that can satisfy the above conditions include combinations of a liquid rubber having a functional group and a crosslinking agent as shown in Table 1.
第1表
液状ゴムの官能基
OH
架橋剤の官能基
NGO
υ
金N酸化物、−011,−NGO
R2
金属酸化物、 −NGOパーオキサイド多情ハロゲン化
合物(−Br)
NGO
0)1.−NH,、−NHR−COOR−5Rr
NRz、 −NHR,−Nl(z、全8M化物C−0R
鳳
NH2
これらは、常温反応性の硬化速度のコントロールの容易
さ、コスト面、入手の容易さ等を含めて考慮すると、特
に水酸基を末端に有し、主鎖をポリブタジェン、水素添
加ポリブタジェン、ポリブタジェン−ニトリル、ポリブ
タジェン−スチレン、イソプレン等や、ポリエーテルポ
リオール、ポリエステルポリオール、ウレタンアクリル
ポリオール、アニリン誘導体ポリオール等を単独、若し
くは併用して用いるのが望ましく、又、難燃性を付与す
るために、水酸基末端液状クロロブレンゴムを添加、或
いは単独で用いるのが望ましい。又、前記反応性物質の
硬化剤としては、イソシアネート系硬化剤が好適であり
、一分子当たり二個以上のインシアネート基を存するこ
とが必要である。Table 1 Functional group OH of liquid rubber Functional group of crosslinking agent NGO υ Gold N oxide, -011, -NGO R2 Metal oxide, -NGO peroxide polyvalent halogen compound (-Br) NGO 0)1. -NH,, -NHR-COOR-5Rr NRz, -NHR, -Nl(z, all 8M compound C-0R OtoriNH2 In particular, polyols with a hydroxyl group at the end and a main chain such as polybutadiene, hydrogenated polybutadiene, polybutadiene-nitrile, polybutadiene-styrene, isoprene, etc., polyether polyols, polyester polyols, urethane acrylic polyols, aniline derivative polyols, etc. It is desirable to use these alone or in combination, and in order to impart flame retardancy, it is desirable to add hydroxyl group-terminated liquid chloroprene rubber or to use it alone.Also, as a curing agent for the above-mentioned reactive substance As such, isocyanate-based curing agents are suitable, and it is necessary that two or more incyanate groups exist per molecule.
その具体例としては、トルイレンジイソシアネート、ジ
フェニルメタンジイソシアネート、ヘキサメチレンジイ
ソシアネート、イソホロンジイソシアネート、両末端に
イソシアネート基を有するプレポリマーを挙げることが
でき、単独、若しくは併用して用いることもできる。又
、イソシアネート系硬化剤は、配合比率、及び粘性等の
問題で可塑剤と混合して用いることもできるが、可塑剤
は、脱水処理したものであることとイソシアネート基と
反応しないことが必要である。上記の常温反応せしめる
上での必須成分のみの組み合せで本発明を満足し得るゴ
ム粘弾性体を得ることもできるが、コスト面、作業性面
、物性向上の面で更に各種の添加剤を加えることより、
幅広い安定したゴム粘弾性体を得ることができる。Specific examples thereof include toluylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, and prepolymers having isocyanate groups at both ends, which can be used alone or in combination. Also, isocyanate curing agents can be used in combination with plasticizers due to problems such as blending ratio and viscosity, but the plasticizers must be dehydrated and must not react with isocyanate groups. be. Although it is possible to obtain a rubber viscoelastic body that satisfies the present invention by combining only the essential components for the room-temperature reaction described above, various additives may be added in order to improve cost, workability, and physical properties. Above all,
A wide range of stable rubber viscoelastic bodies can be obtained.
本発明のゴム粘弾性体を満足し得る添加剤には、例えば
可塑剤、充填剤、瀝青物、粘着付与樹脂、老化防止剤、
防カビ剤、難燃材、触媒、界面活性剤、カップリング剤
、水等の発泡剤或いは消泡剤等が含まれ、その配合量は
可塑剤50〜300 phr、充填剤10〜500 p
hr 、 ’1m青物20〜300 phr 、粘着付
与樹脂0〜100 phrが好ましい。Additives that can satisfy the rubber viscoelastic body of the present invention include, for example, plasticizers, fillers, bituminous substances, tackifying resins, anti-aging agents,
Contains anti-mold agents, flame retardants, catalysts, surfactants, coupling agents, foaming agents such as water, anti-foaming agents, etc., and the blending amounts are 50-300 phr of plasticizer and 10-500 phr of filler.
hr, '1m greens 20-300 phr, and tackifying resin 0-100 phr are preferred.
可塑剤は、粘度調整、作業性調整、ゴム粘弾性体の物性
調整、難燃性の付与等を目的として配合されるものであ
り、50〜300 phr量の添加に依り所望の物性を
得る。300 phr以上では、可塑剤のブリードに依
り形状維持力が低下し、即ち復元力が劣り、一方、50
phr以下では上記目的が達成できない。The plasticizer is blended for the purpose of adjusting the viscosity, adjusting the workability, adjusting the physical properties of the rubber viscoelastic body, imparting flame retardance, etc., and obtains the desired physical properties by adding it in an amount of 50 to 300 phr. Above 300 phr, the shape retention is reduced due to plasticizer bleed, that is, the restoring force is poor;
If the amount is less than phr, the above purpose cannot be achieved.
可塑剤としては、例えばナフテン系オイル、パラフィン
系オイル、アロマチック系オイル、ひまし油、綿実油、
パインオイル、トール油、フタル酸誘導体、マレイン酸
誘導体、官能基を有さない液状ゴム等があり、単独又は
併用して用いることができる。又、難燃性を要する場合
には、ハロゲン化合物系、リン化合物系可塑剤を単独、
又は併用して使用することにより難燃性を付与すること
もできる。Examples of plasticizers include naphthenic oil, paraffinic oil, aromatic oil, castor oil, cottonseed oil,
Examples include pine oil, tall oil, phthalic acid derivatives, maleic acid derivatives, and liquid rubbers without functional groups, which can be used alone or in combination. In addition, if flame retardancy is required, halogen compound-based or phosphorus compound-based plasticizers may be used alone or
Alternatively, flame retardancy can be imparted by using them in combination.
瀝青物としては、例えばストレートアスファルト、プロ
ニアスフアルド、タール等があり、所望のゴム粘弾性体
を得るために、20〜300 phrの量の添加が望ま
しく、予め粘着付与樹脂や、可塑剤等で改質して使用す
ることもできる。Examples of bituminous substances include straight asphalt, proniasphald, tar, etc. In order to obtain the desired rubber viscoelastic body, it is desirable to add 20 to 300 phr of the bituminous material. It can also be modified and used.
粘着付与樹脂としては、例えば天然樹脂、ロジン、変性
ロジン、ロジン及び変性ロジンの誘導体、ポリテルペン
樹脂、テルペン変性体、脂肪族系炭化水素樹脂、シクロ
ペンタジェン系樹脂、芳香族系石油樹脂、フェノール樹
脂、アルキルフェノール−アセチレン樹脂、キシレン樹
脂、クマロン−インデン樹脂、ビニルトルエン−αメチ
ルスチレン共重合体等を0〜100 phr量で単独、
又は併用して添加することにより、繊維への密着力を高
めることができる。Examples of tackifying resins include natural resins, rosins, modified rosins, derivatives of rosins and modified rosins, polyterpene resins, modified terpenes, aliphatic hydrocarbon resins, cyclopentadiene resins, aromatic petroleum resins, and phenolic resins. , alkylphenol-acetylene resin, xylene resin, coumaron-indene resin, vinyltoluene-α-methylstyrene copolymer, etc. alone in an amount of 0 to 100 phr,
Alternatively, by adding them in combination, the adhesion to the fibers can be increased.
充填剤は、約500 phr程度の添加も可能であるが
作業性、物性の点から10〜100 phrの添加が望
ましく、添加により振動減衰性、遮音性、難燃性の改善
に効果があり、主剤/硬化剤の配合比率の調整、粘度の
調整、配合コストダウンを図る目的で使用するものであ
り、ゴム及び塗料関係で一般に使用されるものが好まし
く、例えば、マイカ、グラファイト、ヒル石、タルク、
クレー等の鱗片状無機粉体、炭酸カルシウム、微粉シリ
カ、カーボン、炭酸マグネシウム、水酸化アルミニウム
、アスベスト等の汎用充填剤を単独、若しくは併用して
使用できる。The filler can be added in an amount of about 500 phr, but from the viewpoint of workability and physical properties, it is preferable to add the filler in an amount of 10 to 100 phr.Addition of the filler is effective in improving vibration damping properties, sound insulation properties, and flame retardancy. It is used for the purpose of adjusting the blending ratio of main ingredient/curing agent, adjusting viscosity, and reducing blending costs, and preferably those commonly used in rubber and coatings, such as mica, graphite, vermiculite, and talc. ,
Scale-like inorganic powder such as clay, general-purpose fillers such as calcium carbonate, finely divided silica, carbon, magnesium carbonate, aluminum hydroxide, and asbestos can be used alone or in combination.
また、充填剤にフェライト粉、金属粉、硫酸バリウムを
200 phr以上に加えることにより、比重を2.3
以上とすることができ、高比重シートを得ることができ
る。比重が高ければ高い程、つまり面密度が高ければ高
い程、振動を伝えにくくなるが、粘度や配合比の作業性
及び硬化物の物性を考え合わせると300〜500 p
hrの添加が望ましい。In addition, by adding ferrite powder, metal powder, and barium sulfate to the filler at 200 phr or more, the specific gravity can be reduced to 2.3.
The above can be used, and a high specific gravity sheet can be obtained. The higher the specific gravity, that is, the higher the areal density, the more difficult it is to transmit vibrations, but considering the workability of viscosity and blending ratio, and the physical properties of the cured product, it is 300 to 500 p.
It is desirable to add hr.
一方、本発明のゴム粘弾性体の主成分を、水酸基末端液
状クロロプレンゴムに置換せしめたり、難燃性可塑剤で
ある塩化パラフィンを50〜200phr 、難燃剤で
ある水酸化アルミニウムを50〜200 phr置換せ
しめることにより、難燃性ゴム粘弾性体を得ることがで
き、更に酸化アンチモンやホウ酸亜鉛等を5〜10 p
hr添加することにより、より高い難燃化が可能となる
。また、各々の配合量を多くすると難燃効果も大きくな
るが、コスト、作業性を考慮すると上記配合量が望まし
い。On the other hand, the main components of the rubber viscoelastic body of the present invention are replaced with hydroxyl group-terminated liquid chloroprene rubber, 50 to 200 phr of chlorinated paraffin, which is a flame retardant plasticizer, and 50 to 200 phr, aluminum hydroxide, which is a flame retardant. By substitution, a flame-retardant rubber viscoelastic body can be obtained, and 5 to 10 p of antimony oxide, zinc borate, etc.
By adding hr, higher flame retardance can be achieved. Further, the flame retardant effect increases as the amount of each compounded increases, but the above-mentioned amounts are desirable in consideration of cost and workability.
また、水や低級アルコールを、1〜5 phr添加する
ことにより、発泡ゴム粘弾性体を得ることができるが、
多量に配合すると10倍以上の高い発泡倍率を示し、復
元性や形状維持性に問題が起き不適当であり、少量すぎ
ると10%以下の発泡倍率となり、発泡させることによ
るコスト、振動減衰性の効果を発揮することができず好
ましくない。In addition, a foamed rubber viscoelastic body can be obtained by adding 1 to 5 phr of water or lower alcohol.
If too large a quantity is added, the foaming ratio will be as high as 10 times or more, causing problems with recovery and shape retention, making it inappropriate. If too small a quantity is added, the foaming ratio will be less than 10%, which will reduce the cost of foaming and reduce vibration damping properties. It is undesirable because it cannot be effective.
以上、ゴム粘弾性体について述べたが、粘弾性体の硬度
については、非常に圧縮応力や衝l!緩衝力、復元性に
与える影響も太き(、目的、用途に応じて上記した材料
を選ぶ必要がある。As mentioned above, the rubber viscoelastic body has been described, but the hardness of the viscoelastic body is affected by compressive stress and impact! The materials mentioned above must be selected depending on the purpose and use, as they have a significant influence on the buffering force and restorability.
本発明で用いる繊維状物とは、ポリエステル、ポリエチ
レン、ポリプロピレン、アクリル、ビニロン、レーヨン
、ナイロン、ポリアミド等の合成繊維や紐、綿、パーム
等の天然繊維、ステンレス、アルミニウム、鉄等の金属
繊維やグラスウール、グラスファイバー、カーボン、セ
ラミック等の無機繊維からなる繊維状物の一種又は併用
したものを称し、かかる繊維状物自体が、中空であるも
のや、SBR等の樹脂コーティングしたものであっても
よい。又、厚みは、所望する緩衝シートの厚みにより、
任意に選ぶことができるが、コスト面を考えると、14
m〜4■の厚みが望ましい。又この繊維状物の片面にポ
リエステル、EVA、ポリエチレンのフィルムラミネー
トや、これらの発泡体やウレタン発泡物を積層してもよ
い。The fibrous materials used in the present invention include synthetic fibers and strings such as polyester, polyethylene, polypropylene, acrylic, vinylon, rayon, nylon, and polyamide, natural fibers such as cotton and palm, metal fibers such as stainless steel, aluminum, and iron. Refers to one type of fibrous material or a combination of inorganic fibers such as glass wool, glass fiber, carbon, and ceramic, even if the fibrous material itself is hollow or coated with a resin such as SBR. good. Also, the thickness depends on the desired thickness of the buffer sheet.
You can choose arbitrarily, but considering the cost, 14
A thickness of m to 4 cm is desirable. Further, a film laminate of polyester, EVA, or polyethylene, a foam thereof, or a urethane foam may be laminated on one side of this fibrous material.
繊維状物の厚み方向の一部、若しくは全体にゴム粘弾性
体を含浸させた緩衝シートの片面、若しくは両面に積層
するフィルム状物は、拘束材としても働き、その具体例
を挙げると、ポリエステル、ポリエチレン、塩化ビニル
、EVA等のフィルム状物又はこれらの発泡シート状物
、CR,EPT。A film-like material laminated on one or both sides of a buffer sheet in which part or all of the thickness of the fibrous material is impregnated with a rubber viscoelastic material also acts as a restraining material. , film-like materials such as polyethylene, vinyl chloride, EVA, or foamed sheet-like materials thereof, CR, EPT.
IIR等のシート状物又はこれらの発泡シート状物又は
不織布、割布、ガラスクロス、寒冷紗、紙類等のフィル
ム状物や、鉄、銅、アルミニウム、鉛、ステンレス等の
金属フィルム状物を用いることができ、第4図の如く化
粧加工の有無形状、穴の有無に拘らず使用できるが、可
能な限りヤング率の高い材質が好ましい。Use sheet-like materials such as IIR, foamed sheet-like materials thereof, film-like materials such as non-woven fabric, split cloth, glass cloth, cheesecloth, paper, etc., and metal film-like materials such as iron, copper, aluminum, lead, stainless steel, etc. As shown in FIG. 4, it can be used regardless of whether or not it has a decorative finish, shape, or hole, but it is preferable to use a material with as high a Young's modulus as possible.
(実施例及び比較例)
本発明を実施例及び比較例により詳述し、後述する評価
方法を用いて評価し、結果を第2表に示した。(Examples and Comparative Examples) The present invention will be explained in detail using Examples and Comparative Examples, and evaluated using the evaluation method described below. The results are shown in Table 2.
実JJL上
水酸基末端液状ポリブタジェン、アスファルト、可塑剤
を基本成分とする主剤とイソシアネート基を1分子当た
り2個以上有する硬化剤を混合したゴム粘弾性体を、繊
維状物の一例である不織布の全体へ含浸させ、硬化反応
せしめて繊維入りゴムシートを得る。該シートは良好な
圧縮特性や復元性を示す。又、木質仕上げ床に適用して
も充分な性能を示すものである。A rubber viscoelastic body prepared by mixing a main ingredient consisting of hydroxyl group-terminated liquid polybutadiene, asphalt, and a plasticizer with a curing agent having two or more isocyanate groups per molecule is used as a whole nonwoven fabric, which is an example of a fibrous material. A rubber sheet containing fibers is obtained by impregnating the fiber into a rubber sheet and subjecting it to a curing reaction. The sheet exhibits good compression properties and recovery properties. It also shows sufficient performance even when applied to wooden finished floors.
裏旌班I
水酸基末端液状ポリブタジェン、アスファルト、可塑剤
を基本成分とする主剤とイソシアネート基を1分子当た
り二個以上有する硬化剤を混合したゴム粘弾性体を、繊
維状物の一例である不織布の厚み方向の一部へ含浸させ
、硬化反応せしめて繊維入りゴムシートを得る。該シー
トは、良好な圧縮特性や復元性を示す。木質仕上げ床に
適用しても充分な性能を示すものである。Urajoban I A rubber viscoelastic material prepared by mixing a main ingredient consisting of hydroxyl-terminated liquid polybutadiene, asphalt, and a plasticizer, and a curing agent having two or more isocyanate groups per molecule, is used as a nonwoven fabric, which is an example of a fibrous material. A part of the thickness is impregnated and a curing reaction is performed to obtain a fiber-filled rubber sheet. The sheet exhibits good compression properties and recovery properties. It shows sufficient performance even when applied to wooden finished floors.
1隻貫主
水酸基末端液状ポリブタジェン、アスファルト、難燃性
可塑剤を基本成分とした主剤とイソシアネート基を1分
子当たり二個以上有する硬化剤を混合したゴム粘弾性体
を、繊維状物の一例である不織布全体へ含浸させ、硬化
反応せしめて繊維入りゴムシートを得る。該シートも良
好な圧縮特性や復元性を示すと同時に、良好な難燃性を
有する。An example of a fibrous material is a rubber viscoelastic material that is a mixture of a main component consisting of a single main hydroxyl group-terminated liquid polybutadiene, asphalt, and a flame-retardant plasticizer, and a curing agent having two or more isocyanate groups per molecule. The entire nonwoven fabric is impregnated and a curing reaction is performed to obtain a fiber-filled rubber sheet. The sheet also exhibits good compression properties and recovery properties, and at the same time has good flame retardancy.
又、木質仕上げ床に適用しても充分な性能を示すもので
ある。It also shows sufficient performance even when applied to wooden finished floors.
夫旌炎土
水酸基末端液状ポリブタジェン、アスファルト、可塑剤
及び高比重充填材として金属スラッジを基本成分とする
主剤とイソシアネート基を1分子当たり二個以上有する
硬化剤を混合したゴム粘弾性体を、繊維状物の一例であ
る不織布全体へ含浸させ硬化せしめて繊維入りゴムシー
トを得る。良好な圧縮特性や復元性を示しており、特に
木質仕上床に適用した場合に、軽量衝撃音レベルと重量
床衝撃音レベルの双方を改善できる。A rubber viscoelastic body is prepared by mixing a rubber viscoelastic body with a base component consisting of hydroxyl group-terminated liquid polybutadiene, asphalt, a plasticizer, and metal sludge as a high-density filler, and a curing agent having two or more isocyanate groups per molecule. A rubber sheet containing fibers is obtained by impregnating the entire nonwoven fabric, which is an example of a nonwoven fabric, and curing it. It shows good compression properties and recovery properties, and can improve both light impact sound level and heavy floor impact sound level, especially when applied to wood-finished floors.
尖旌■旦
水酸基末端液状ポリブタジェン、アスファルト、可塑剤
及び発泡剤となる水を基本成分とする主剤とイソシアネ
ート基を1分子当たり二個以上有する硬化剤を混合した
ゴム粘弾性体を繊維状物の一例である不織布の全体へ含
浸させ発泡硬化せしめて繊維入りゴムシートを得る。該
シートは、良好な圧縮特性を示し、復元性、80″C形
状保持性については、若干、発泡していないゴム粘弾性
体に劣るが、木質仕上床に適用できるものである。A fibrous material is made of a rubber viscoelastic material that is a mixture of hydroxyl group-terminated liquid polybutadiene, asphalt, a plasticizer, a water-based base ingredient as a plasticizer, and a curing agent having two or more isocyanate groups per molecule. For example, a nonwoven fabric is completely impregnated and foamed and cured to obtain a fiber-filled rubber sheet. The sheet exhibits good compression properties, and although it is slightly inferior to non-foamed rubber viscoelastic materials in terms of resilience and 80''C shape retention, it can be applied to wood-finished floors.
裏蓋IL
ウレタンを基本成分とした粘弾性体を、不織布全体へ含
浸させ、硬化せしめて繊維入りゴムシートを得る。該シ
ートは、良好な圧縮特性を示し、高温下でも充分使用で
きる。又、木質仕上床に適用しても充分な性能を示すも
のである。Back cover IL A viscoelastic material containing urethane as a basic component is impregnated into the entire nonwoven fabric and cured to obtain a fiber-filled rubber sheet. The sheet exhibits good compression properties and can be used satisfactorily even at high temperatures. It also shows sufficient performance even when applied to wooden finished floors.
実施拠工
本例においては、粘弾性体が、エマルジョン系粘弾性体
より成る架橋粘弾性体であり、実施例1と同様な繊維入
りゴムシートを得る。該シートは、良好な圧縮特性を示
す。又、木質仕上床に適用しても充分な性能を示すもの
である。In this example, the viscoelastic body is a crosslinked viscoelastic body made of an emulsion-based viscoelastic body, and a fiber-filled rubber sheet similar to that of Example 1 is obtained. The sheet exhibits good compression properties. It also shows sufficient performance even when applied to wooden finished floors.
実JL[L亀
スチレン−イソプレン−スチレン共重合体を基本ポリマ
ーとしたゴム粘弾性体を不織布全体へ含浸させるが、架
橋は行なわれない。この場合は8゜℃の形状保持性が若
干劣るものの、加熱された状態で使用しない場合は充分
使用可能であり、また充分な圧縮特性を示す。A rubber viscoelastic material whose basic polymer is a styrene-isoprene-styrene copolymer is impregnated into the entire nonwoven fabric, but crosslinking is not performed. In this case, although the shape retention at 8° C. is slightly inferior, it can be used satisfactorily if it is not used in a heated state, and also exhibits sufficient compression characteristics.
北較■上
比較例としてゴム粘弾性体がなく、不織布単体の場合を
示す。かかる場合は、圧縮特性が低くなり、復元性が大
幅に劣り、本発明の目的を達成できないものであり好ま
しくない。Northern Comparison ① As a comparative example above, there is no rubber viscoelastic material, and a case in which a nonwoven fabric alone is used is shown. In such a case, the compression characteristics become low and the restorability is significantly inferior, making it impossible to achieve the object of the present invention, which is not preferable.
北本1−
ゴム粘弾性体単体の場合であり、圧縮特性、復元性は良
好ではあるが、木質仕上げ床に適応した場合、充分な効
果を奏せず、本発明の目的を達成できないものであり、
好ましくない。Kitamoto 1 - This is the case of a single rubber viscoelastic body, and although it has good compression properties and restorability, it does not have sufficient effects when applied to a wood-finished floor, and the purpose of the present invention cannot be achieved. ,
Undesirable.
北較■ユ
本発明に用いるゴム粘弾性体が、温度20℃の条件下で
硬度がC型硬度計(日本ゴム協会規格SRT S−01
01)で40になるように調整した水酸基末端液状ポリ
ブタジェン、短鎖ジオール、アスファルト、充填剤を基
本成分とする主剤と、イソシアネート基を1分子当り二
個以上有する硬化剤を混合したものを、不織布へ全体に
含浸させ、硬化せしめて得られる場合を示し、良好な圧
縮特性や復元性を有しているが、木質仕上げ床に適用し
た場合、期待する効果を奏せず、本発明の目的を達し得
ないものであり好ましくない。The hardness of the rubber viscoelastic body used in the present invention at a temperature of 20°C was determined by a C-type hardness tester (Japan Rubber Association standard SRT S-01).
A non-woven fabric is prepared by mixing a main ingredient consisting of hydroxyl-terminated liquid polybutadiene, short-chain diol, asphalt, and a filler, adjusted to have a concentration of 40 in step 01), and a curing agent having two or more isocyanate groups per molecule. This shows a case obtained by impregnating the entire surface of the wood and hardening it, and it has good compression properties and recovery properties, but when applied to a wooden finished floor, it does not have the expected effect, and the purpose of the present invention is not achieved. It is unattainable and undesirable.
*1 水酸基末端液状ポリブタジェン
出光石油化学■製
商品名 Po1y Bd R−45HT*2 ポリエー
テルポリオール
第一工業製薬■製
商品名 ポリハードナーD−350
*3 アクリルエマルジョン
中央理化工業■製
商品名 リカボンド P S −8000A*4 ゴム
・アスファルトエマルジョン日本ラテックス加工■製
商品名 ハルコート
*5 スチレン−イソプレン−スチレン共重合体シェル
化学■製
商品名 フィントン1107
*6 再生ブチルゴム
早用ゴム■製
商品名 低ムーニー再生ブチル
*7 短鎖ジオール
商品名 アイリノールC−100
*8可塑剤A
出光石油化学■製
商品名 ダイアナプロセスオイルAH−16*9可塑剤
B
東京樹脂工業■製
商品名 U−レックス180EF
*10可塑剤C
味の素■製 商品名 エンパラ45
*11 粘着付与樹脂a
安原油脂■製
商品名 YS−レジン A−800
*12 粘着付与樹脂す
荒用化学■製
商品名 アルコンP−100
*13触 媒
日本化学産業■製
商品名 オクチル酸スズ
*14
*15
イソシアネートプレポリマー
第一工業製薬■製
商品名 ポリフレックスMH
アジリジン化合物
ジフェニルメタン−ビス−4,4’ −N、N ’−ジ
エチレン尿素
評価方法
8課」1
実施例及び比較例に示す配合処方に沿ってゴム粘弾性体
の主剤を調整し、所定の硬化剤を混合したものを不織布
に含浸させ硬化せしめるか、主剤を不織布に含浸させ乾
燥固化せしめることにより繊維入りゴムシートを得る。*1 Hydroxyl group-terminated liquid polybutadiene manufactured by Idemitsu Petrochemical ■Product name Poly Bd R-45HT*2 Polyether polyol manufactured by Daiichi Kogyo Seiyaku ■Product name Polyhardener D-350 *3 Acrylic emulsion manufactured by Chuo Rika Kogyo ■Product name Ricabond P S -8000A*4 Rubber/asphalt emulsion Made by Japan Latex Processing ■Product name: Hullcoat*5 Styrene-isoprene-styrene copolymer Shell Chemical ■Product name: Finton 1107 *6 Recycled butyl rubber Early use rubber ■Product name: Low Mooney Recycled butyl* 7 Short-chain diol Product name Airinol C-100 *8 Plasticizer A Made by Idemitsu Petrochemical ■ Product name Diana Process Oil AH-16 *9 Plasticizer B Made by Tokyo Jushi Kogyo ■ Product name U-Rex 180EF *10 Plasticizer C Made by Ajinomoto ■ Product name Empara 45 *11 Tackifying resin a Made by cheap crude oil ■ Product name YS-Resin A-800 *12 Tackifying resin manufactured by Suurayo Kagaku ■ Product name Alcon P-100 *13 Catalyst Nippon Kagaku Sangyo ■ Product name: Tin octylate *14 *15 Isocyanate prepolymer Daiichi Kogyo Seiyaku ■ Product name: Polyflex MH Aziridine compound diphenylmethane-bis-4,4'-N,N'-diethylene urea evaluation method Section 8"1 Example The main ingredient of the rubber viscoelastic body is adjusted according to the formulation shown in the Comparative Example, and a predetermined curing agent is mixed therewith and then impregnated into a nonwoven fabric and cured. Alternatively, the main ingredient is impregnated into a nonwoven fabric and dried and solidified. Get a rubber sheet.
L硬皮画定
1251m厚X12Osm幅X100 sm長さの試料
を作製し、硬度測定用試料とした。室温で7日、50℃
雰囲気中で7日の養生を行なった後、JIS−に−63
01に準じ20℃で硬度の測定を行なった。A sample with L hard skin definition of 1251 m thick x 12 osm width x 100 sm length was prepared and used as a sample for hardness measurement. 7 days at room temperature, 50℃
After 7 days of curing in the atmosphere, the JIS-63
The hardness was measured at 20° C. according to 01.
影80”C膝世鉦1法
3〇−高さ×50φの大きさに調整した試料を作製し、
弾性面に離型紙を当てて、500gの荷重をかけて80
℃×24時間の条件下で静置した後、除荷し室温に静置
し、4時間後の変型の大小を目視により判定した。エツ
ジ部がシャープで変形の少ないものをO印、エツジ部の
シャープさが無いもの、変形の大きいものをX印で示し
た。Create a sample adjusted to the size of shadow 80"C knees 1 method 30-height x 50φ,
Apply a release paper to the elastic surface and apply a load of 500g to the
After being left at rest under conditions of 24 hours at ℃, the load was unloaded and left at room temperature, and the degree of deformation after 4 hours was visually determined. Those with sharp edges and little deformation are marked O, and those with sharp edges and large deformations are marked X.
虹沫jI111定
150 mmRCスラブ7に対し、第5図で示す如く繊
維状物2の一部にゴム粘弾性体重を含浸し、5.5■■
化粧板6を積層し、被衝撃面7に貼付したちの16を、
タッピングマシン10により軽量術Ifを測定し、パン
ダマシン11により重量衝撃音を測定した。測定方法は
、J I 5−A−1418に準じ、第6図に示す方法
を行なった。12はマイクロホン、13は精密騒音計、
14は周波数分析器、15はレベルコーダーを示す。尚
、結果はJ I 5−A−1419に準じ床衝撃音の遮
音等級により示した。As shown in FIG. 5, a part of the fibrous material 2 is impregnated with rubber viscoelastic weight for the 150 mm RC slab 7 of 5.5 mm.
The decorative board 6 is laminated and attached to the impact surface 7.
The weight impact sound was measured using the tapping machine 10 and the weight impact sound using the panda machine 11. The measurement method was as shown in FIG. 6 in accordance with J I 5-A-1418. 12 is a microphone, 13 is a precision sound level meter,
14 is a frequency analyzer, and 15 is a level coder. The results were shown in terms of floor impact sound insulation grade according to JI 5-A-1419.
」−ミー性
5011II幅X 50m+m長さの試料を、上下に離
型紙を当てて圧縮試験機により、圧縮速度2mm/分に
て50%圧縮し、30分間保持した後、除荷し、10分
後の復元性をチエツクした。95%以上の復元性を示し
たものを○印、90%以上の復元性を示したものをΔ印
、90%以下の復元性を示したものをX印で示した。- A sample of Mie property 5011 II width x 50 m + length was compressed by 50% at a compression speed of 2 mm/min using a compression tester with release paper placed on the top and bottom, held for 30 minutes, then unloaded for 10 minutes. I checked the restorability afterward. Those that showed a restorability of 95% or more were marked with a circle, those that showed a restorability of 90% or more were marked with a Δ, and those that showed a restorability of 90% or less were marked with an X.
も上Ji咀
繊維入りゴムシート試料の圧縮応力と変位の関係を圧縮
試験機により、圧縮速度2Illl/分の条件にて圧縮
し、得られたチャートより変位と圧縮応力を読み取り第
7図に示した。The relationship between compressive stress and displacement of a rubber sheet sample containing fibers was compressed using a compression tester at a compression rate of 2 Ill/min, and the displacement and compressive stress were read from the obtained chart and shown in Figure 7. Ta.
互葺笠斐合図
繊維入りゴムシート試料を、GIIII1幅X10cm
+長さに切断し、J I S−に−7201に準じ、酸
素指数の測定を行なった。A sample of rubber sheet with fibers, GIII1 width x 10cm
The sample was cut into + lengths, and the oxygen index was measured according to JIS-7201.
しルーー重
1c纏X1cmの大きさに切断した試料を、JIS−K
−6350−6−1による水中懸架方法に従って比重
の測定を行なった。JIS-K
The specific gravity was measured according to the underwater suspension method according to -6350-6-1.
第7図のIは、本発明におけるゴム粘弾性体の有無、及
び繊維状物の有無による圧縮特性の差について示す。I in FIG. 7 shows the difference in compression properties depending on the presence or absence of a rubber viscoelastic body and the presence or absence of a fibrous material in the present invention.
繊維入りゴムシートの圧縮特性と、ゴム帖弾性体単体、
不織布単体との圧縮特性を比較してみると、変位がある
程度の範囲までは不織布単体とほぼ同程度のわずかな圧
縮荷重しか要しないが、大きな変位の場合には、大きな
圧縮荷重を必要とすることがわかる。すなわち、小さな
圧縮荷重では変位し易く、大きな圧縮荷重では変位し難
くなることを示しており、衝撃緩衝シート・とじては理
想的な圧縮特性である。Compression properties of fiber-filled rubber sheets, rubber sheet elastic body alone,
Comparing the compression characteristics with nonwoven fabric alone, it is found that up to a certain range of displacement, only a small compressive load is required, which is almost the same as that of nonwoven fabric alone, but in the case of large displacement, a large compressive load is required. I understand that. In other words, it shows that it is easy to displace under a small compressive load, and difficult to displace under a large compressive load, which is the ideal compression characteristic for an impact cushioning sheet.
(発明の効果)
以上説明してきたように、本発明の繊維入りゴムシート
は、ゴム粘弾性体の持つ圧縮特性と繊維状物の持つ圧縮
特性を利用し、繊維状物の厚み方向に対して、一部若し
くは全体を含浸することにより、即ち繊維状物の網目構
造内にゴム粘弾性体が入り込むことにより、繊維とゴム
粘弾性体との接触面積を増大させることとなり、ズリ変
形による衝l!緩和、制振効果を効率よく発揮させるこ
とができるもので、ゴム粘弾性体の作業性を改善でき、
ゴム帖弾性体自体の節約にもなり低コスト化を実現し、
ゴム粘弾性体の難燃化、高比重化等の付加価値を付は易
い等の応用用途が広くなる効果を有する。(Effects of the Invention) As explained above, the fiber-containing rubber sheet of the present invention utilizes the compression properties of the rubber viscoelastic body and the compression properties of the fibrous material, and uses the compression properties of the fibrous material in the thickness direction. By impregnating a part or all of the fibrous material, that is, the rubber viscoelastic material enters into the network structure of the fibrous material, the contact area between the fiber and the rubber viscoelastic material is increased, and the impact caused by shear deformation is increased. ! It can efficiently exert the relaxation and damping effect, and it can improve the workability of rubber viscoelastic bodies.
It also saves on the rubber band elastic body itself, reducing costs.
It has the effect of widening the range of applications, such as making it easy to add added values such as making the rubber viscoelastic body flame retardant and increasing specific gravity.
第1図は、繊維状物全体にゴム粘弾性体が含浸され、被
衝撃面に貼付された本発明の繊維入りゴムシートの好適
例の断面図、
第2図は、繊維状物の一部にゴム粘弾性体が含浸され、
被衝撃面に貼付された本発明の繊維入りゴムシートの好
適例の断面図、
第3図は、繊維状物の一部にゴム粘弾性体が含浸され、
拘束材層を積層し、被衝撃面に貼付された本発明の繊維
入りゴムシートの好適例の断面図、第4図は、繊維状物
の一部にゴム粘弾性体が含浸され、その両面に拘束材層
が積層され、被衝撃面に貼付された本発明の繊維入りゴ
ムシートの好適例の断面図、
第5図は、繊維状物の一部にゴム粘弾性体が含浸されて
おり、化粧合板を積層し、被衝撃面に貼付された本発明
に係る床衝撃音測定に供した試験体の一例の構成断面図
、
第6図は、本発明に係る床衝撃音の測定を行なった装置
を示す図、
第7図は、本発明に係る繊維入りゴムシートの圧縮特性
を示した線図である。
1・・・ゴム粘弾性体 2・・・繊維状物3・・・
拘束層(ポリエステルフィルム)4・・・被衝撃面
5・・・拘束層(有孔鉄板)
6・・・5.5m園化粧合板 7・・・150 s+
a床スラブ8・・・受音室 9・・・音源室
10・・・タッピングマシン 11・・・バングマシン
12・・・マイクロホン 13・・・精密騒音計1
4・・・周波数分析器 15・・・レベルレコーダ
ー16・・・供試体
第1図
第7図
1.0
1し、*(mmンFIG. 1 is a cross-sectional view of a preferred example of a fiber-filled rubber sheet of the present invention in which the entire fibrous material is impregnated with a rubber viscoelastic material and is affixed to an impact surface. FIG. 2 is a portion of the fibrous material. is impregnated with rubber viscoelastic material,
FIG. 3 is a cross-sectional view of a preferred example of the fiber-containing rubber sheet of the present invention attached to the impact surface, in which a portion of the fibrous material is impregnated with a rubber viscoelastic material,
FIG. 4 is a cross-sectional view of a preferred example of the fiber-filled rubber sheet of the present invention in which a restraining material layer is laminated and applied to an impact surface, and a portion of the fibrous material is impregnated with a rubber viscoelastic material, and both sides of the fiber-filled rubber sheet are shown in FIG. FIG. 5 is a cross-sectional view of a preferred example of the fiber-filled rubber sheet of the present invention, in which a restraining material layer is laminated on the impact surface and the rubber sheet is affixed to the impact surface. FIG. 6 is a cross-sectional view of an example of a test specimen made of laminated decorative plywood and attached to the impact surface, which was used for floor impact sound measurement according to the present invention. FIG. 7 is a diagram showing the compression characteristics of the fiber-filled rubber sheet according to the present invention. 1... Rubber viscoelastic body 2... Fibrous material 3...
Restraint layer (polyester film) 4... Impact surface 5... Restraint layer (perforated iron plate) 6...5.5m Decorative plywood 7...150 s+
a Floor slab 8...Sound receiving room 9...Sound source room 10...Tapping machine 11...Bang machine 12...Microphone 13...Precision sound level meter 1
4...Frequency analyzer 15...Level recorder 16...Specimen Fig. 1 Fig. 7 1.0 1, *(mm)
Claims (1)
又は併用物に対して、その厚み方向の一部、若しくは全
体にゴム粘弾性体を含浸させた繊維入りゴムシートに於
て、ゴム粘弾性体が、80℃に加温されても形状を保持
し、20℃の条件下で硬度がC型硬度計で0〜20であ
ることを特徴とする繊維入りゴムシート。 2、上記ゴム粘弾性体が、発泡硬化せしめられ、その発
泡倍率が1.1〜10倍であることを特徴とする請求項
1記載の繊維入りゴムシート。 3、上記ゴム粘弾性体が、分子の両端に反応基を有する
テレキリックポリマーを主成分とし、常温で液状である
主剤と、主剤のテレキリックポリマーの反応基と反応し
て結合し得る反応基を1分子当たり2個以上有する硬化
剤とを主成分とし、5℃〜80℃の温度域で硬化されて
成ることを特徴とする請求項1記載の繊維入りゴムシー
ト。 4、上記ゴム粘弾性体が、難燃性であることを特徴とす
る請求項1記載の繊維入りゴムシート。 5、上記ゴム粘弾性体が、比重2.3以上であることを
特徴とする請求項1記載の繊維入りゴムシート。 6、上記繊維入りゴムシートの片面、若しくは両面に、
ポリエステル、ポリエチレン、塩化ビニル、エチレン−
酢酸ビニルコポリマー等のフィルム状物又はこれらの発
泡シート状物、クロロプレンゴム、エチレン−プロピレ
ンターポリマー、ブチルゴム、ニトリルゴム等のシート
状物又はこれらの発泡シート状物、又は不織布、割布、
ガラスクロス、寒冷紗、紙類等のフィルム状物や、鉄、
アルミニウム、鉛、銅、ステンレス等の金属フィルム状
物を拘束材として積層して成ることを特徴とする請求項
1記載の繊維入りゴムシート。[Claims] 1. A type of synthetic fiber, natural fiber, metal fiber, or inorganic fiber;
Or for a combination product, in a fiber-containing rubber sheet whose thickness is partially or entirely impregnated with a rubber viscoelastic material, the rubber viscoelastic material retains its shape even when heated to 80°C. A fiber-containing rubber sheet having a hardness of 0 to 20 on a C-type hardness tester at 20°C. 2. The fiber-filled rubber sheet according to claim 1, wherein the rubber viscoelastic body is foam-cured and has a foaming ratio of 1.1 to 10 times. 3. The rubber viscoelastic body is mainly composed of a telechelic polymer having reactive groups at both ends of the molecule, and has a main component that is liquid at room temperature and a reactive group that can react with and bond with the reactive group of the telechelic polymer as the main component. The fiber-containing rubber sheet according to claim 1, characterized in that the fiber-containing rubber sheet contains as a main component a curing agent having two or more of the following per molecule, and is cured at a temperature range of 5°C to 80°C. 4. The fiber-filled rubber sheet according to claim 1, wherein the rubber viscoelastic body is flame retardant. 5. The fiber-filled rubber sheet according to claim 1, wherein the rubber viscoelastic body has a specific gravity of 2.3 or more. 6. On one or both sides of the fiber-filled rubber sheet,
Polyester, polyethylene, vinyl chloride, ethylene-
Film-like products such as vinyl acetate copolymers or foamed sheet-like products thereof, sheet-like products such as chloroprene rubber, ethylene-propylene terpolymer, butyl rubber, nitrile rubber, or foamed sheet-like products thereof, or non-woven fabrics, split cloth,
Film materials such as glass cloth, cheesecloth, and paper, iron,
The fiber-filled rubber sheet according to claim 1, characterized in that it is formed by laminating a metal film-like material such as aluminum, lead, copper, stainless steel, etc. as a restraining material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2161454A JPH0776275B2 (en) | 1990-06-21 | 1990-06-21 | Damping structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2161454A JPH0776275B2 (en) | 1990-06-21 | 1990-06-21 | Damping structure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0453837A true JPH0453837A (en) | 1992-02-21 |
JPH0776275B2 JPH0776275B2 (en) | 1995-08-16 |
Family
ID=15735414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2161454A Expired - Fee Related JPH0776275B2 (en) | 1990-06-21 | 1990-06-21 | Damping structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0776275B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996004651A1 (en) * | 1994-07-29 | 1996-02-15 | Minnesota Mining And Manufacturing Company | Internally-damped rotatable information-storage article |
WO2004036973A1 (en) * | 2002-10-18 | 2004-04-29 | Nisshinbo Industries, Inc. | Conductive cushion material and process for producing the same |
JP2007085461A (en) * | 2005-09-22 | 2007-04-05 | Iida Sangyo Kk | Viscous vibration/shock absorbing raw material |
JP2009242618A (en) * | 2008-03-31 | 2009-10-22 | Sekisui Chem Co Ltd | Foamed sheet of rubber-based resin with closed cell and its manufacturing method |
WO2011105597A1 (en) | 2010-02-23 | 2011-09-01 | Fujifilm Corporation | Back sheet for solar cell, method for producing the same, and solar cell module |
JP2015040900A (en) * | 2013-08-20 | 2015-03-02 | ヤマハ株式会社 | Percussion instrument pad and manufacturing method of percussion instrument pad |
JP2021025572A (en) * | 2019-08-02 | 2021-02-22 | アンビック株式会社 | Viscoelastic body |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61261047A (en) * | 1985-05-15 | 1986-11-19 | 早川ゴム株式会社 | Manufacture of vibration-damping board |
-
1990
- 1990-06-21 JP JP2161454A patent/JPH0776275B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61261047A (en) * | 1985-05-15 | 1986-11-19 | 早川ゴム株式会社 | Manufacture of vibration-damping board |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996004651A1 (en) * | 1994-07-29 | 1996-02-15 | Minnesota Mining And Manufacturing Company | Internally-damped rotatable information-storage article |
US5538774A (en) * | 1994-07-29 | 1996-07-23 | Minnesota Mining And Manufacturing Company | Internally damped rotatable storage article |
USRE36806E (en) * | 1994-07-29 | 2000-08-01 | 3M Innovative Properties Company | Internally damped rotatable storage article |
EP1043719A3 (en) * | 1994-07-29 | 2000-11-22 | Minnesota Mining And Manufacturing Company | Internally-damped rotatable information storage article |
WO2004036973A1 (en) * | 2002-10-18 | 2004-04-29 | Nisshinbo Industries, Inc. | Conductive cushion material and process for producing the same |
JP2007085461A (en) * | 2005-09-22 | 2007-04-05 | Iida Sangyo Kk | Viscous vibration/shock absorbing raw material |
JP2009242618A (en) * | 2008-03-31 | 2009-10-22 | Sekisui Chem Co Ltd | Foamed sheet of rubber-based resin with closed cell and its manufacturing method |
WO2011105597A1 (en) | 2010-02-23 | 2011-09-01 | Fujifilm Corporation | Back sheet for solar cell, method for producing the same, and solar cell module |
JP2015040900A (en) * | 2013-08-20 | 2015-03-02 | ヤマハ株式会社 | Percussion instrument pad and manufacturing method of percussion instrument pad |
CN104424931A (en) * | 2013-08-20 | 2015-03-18 | 雅马哈株式会社 | Electronic percussion pad and method of manufacturing electronic percussion pad |
US9373311B2 (en) | 2013-08-20 | 2016-06-21 | Yamaha Corporation | Method of manufacturing electronic percussion pad |
JP2021025572A (en) * | 2019-08-02 | 2021-02-22 | アンビック株式会社 | Viscoelastic body |
Also Published As
Publication number | Publication date |
---|---|
JPH0776275B2 (en) | 1995-08-16 |
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