JPS6048230B2 - Coating method with self-adhesive elastic layer - Google Patents
Coating method with self-adhesive elastic layerInfo
- Publication number
- JPS6048230B2 JPS6048230B2 JP8427276A JP8427276A JPS6048230B2 JP S6048230 B2 JPS6048230 B2 JP S6048230B2 JP 8427276 A JP8427276 A JP 8427276A JP 8427276 A JP8427276 A JP 8427276A JP S6048230 B2 JPS6048230 B2 JP S6048230B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- lining
- self
- tape
- adhesive
- 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
Links
- 239000000853 adhesive Substances 0.000 title claims description 35
- 238000000576 coating method Methods 0.000 title claims description 20
- 229920005989 resin Polymers 0.000 claims description 56
- 239000011347 resin Substances 0.000 claims description 56
- 239000004744 fabric Substances 0.000 claims description 27
- 239000004570 mortar (masonry) Substances 0.000 claims description 26
- 238000010276 construction Methods 0.000 claims description 25
- 239000011521 glass Substances 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 23
- 239000002390 adhesive tape Substances 0.000 claims description 19
- 239000011248 coating agent Substances 0.000 claims description 17
- 239000003822 epoxy resin Substances 0.000 claims description 13
- 229920000647 polyepoxide Polymers 0.000 claims description 13
- 229920001567 vinyl ester resin Polymers 0.000 claims description 12
- 239000000835 fiber Substances 0.000 claims description 9
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 8
- 238000003825 pressing Methods 0.000 claims description 8
- 239000004745 nonwoven fabric Substances 0.000 claims description 7
- 239000007849 furan resin Substances 0.000 claims description 6
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 5
- 239000004636 vulcanized rubber Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 239000010445 mica Substances 0.000 claims description 3
- 229910052618 mica group Inorganic materials 0.000 claims description 3
- 238000012360 testing method Methods 0.000 description 51
- 239000010410 layer Substances 0.000 description 37
- 239000010408 film Substances 0.000 description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 21
- 239000004567 concrete Substances 0.000 description 19
- 239000003973 paint Substances 0.000 description 16
- 239000002585 base Substances 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 239000010454 slate Substances 0.000 description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 10
- 239000000377 silicon dioxide Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- 239000005060 rubber Substances 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- 238000004073 vulcanization Methods 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- 229920002978 Vinylon Polymers 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 238000005452 bending Methods 0.000 description 5
- 238000005336 cracking Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000004576 sand Substances 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- -1 alkalis Chemical class 0.000 description 4
- 229920005549 butyl rubber Polymers 0.000 description 4
- 239000011247 coating layer Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000035882 stress Effects 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 238000004078 waterproofing Methods 0.000 description 4
- 229930185605 Bisphenol Natural products 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229920006311 Urethane elastomer Polymers 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000009863 impact test Methods 0.000 description 3
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 239000002990 reinforced plastic Substances 0.000 description 3
- 230000003014 reinforcing effect Effects 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-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
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 2
- 150000001412 amines Chemical class 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
- 239000004917 carbon fiber Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 229920002681 hypalon Polymers 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000256297 Euphorbia tirucalli Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 241000617482 Kiwa Species 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 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
- AFSKMUFTKFPHCZ-UHFFFAOYSA-N calcium;oxolead Chemical compound [Ca].[Pb]=O AFSKMUFTKFPHCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 230000005489 elastic deformation Effects 0.000 description 1
- 230000012173 estrus Effects 0.000 description 1
- 230000006355 external stress Effects 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- HDNHWROHHSBKJG-UHFFFAOYSA-N formaldehyde;furan-2-ylmethanol Chemical compound O=C.OCC1=CC=CO1 HDNHWROHHSBKJG-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 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
- 239000002075 main ingredient Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
【発明の詳細な説明】
本発明は自己接着性弾性層を有する被覆施工法に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of applying a coating with a self-adhesive elastic layer.
更に詳しくは鉄、ステンレス、アルミニウムなどの金属
表面およびコンクリート、モルタル、スレートなどの無
機構造材表面の長期保護、防水性、耐薬品性の改善なら
びに耐衝撃性、クッション性を併せ有する被覆の施工法
に関する。従来、鉄やアルミニウムの腐食防止には種々
の塗料が用いられている。For more details, see how to apply coatings that provide long-term protection, improve waterproofing and chemical resistance, and provide impact resistance and cushioning properties for metal surfaces such as iron, stainless steel, and aluminum, as well as inorganic structural material surfaces such as concrete, mortar, and slate. Regarding. Conventionally, various paints have been used to prevent corrosion of iron and aluminum.
しかし塗料塗膜の膜厚は1回塗ではたかだか20〜10
0μを薄く、長期耐食性を得るためには塗料を数回繰返
して塗り重ねる必要があつた。また500〜1000μ
の膜厚を得ることは容易な事ではなく、就中腐食性の著
しい海・洋、海浜或は工業地域の構造物やプラントの長
期耐食性を期待することは困難であつた。特にアングル
や切断個所のエッジ部、溶接部のバリの部分あるいは接
合部の内側などは膜厚が薄くなり易く、発情も早期に見
られた。か)る欠点を改良するためにプラスチツクテー
プの片面に粘着剤を施した粘着テープを用いる方法が提
案されているが、テープの重ね合せ部分が一体化せず間
隙を生ずる欠点があり、オーバーラップした部分と、し
ていない部分の厚さの相違による段差を生するとか、テ
ープの末端や周辺部から剥れ易い欠点があつた。However, the film thickness of the paint film is at most 20 to 10
In order to make the 0μ thinner and obtain long-term corrosion resistance, it was necessary to apply the paint several times. Also 500~1000μ
It is not easy to obtain a film thickness of 100%, and it has been difficult to expect long-term corrosion resistance for structures and plants located in the sea, ocean, beaches, or industrial areas, which are particularly corrosive. In particular, the film thickness tends to be thinner at angles, edges of cut points, burrs at welds, and the inside of joints, and estrus was observed early. In order to improve this problem, a method of using adhesive tape with adhesive applied on one side of plastic tape has been proposed, but it has the disadvantage that the overlapping parts of the tape do not integrate and create gaps, resulting in the overlapping of the tapes. There were disadvantages such as creating a step difference due to the difference in thickness between the tape and the non-covering area, and the tape easily peeling off from the end and periphery.
更に鉄やコンクリート床において耐酸性を付与したり歩
行、走行の滑り止めを目的としたエポキシ樹脂に硅砂な
どを混合し、厚膜に施工して硬化させる樹脂モルタル仕
上げが行れている。Furthermore, a resin mortar finish is used to add acid resistance to iron or concrete floors and to prevent slipping when walking or running, by mixing epoxy resin with silica sand, etc., and applying it to a thick film and curing it.
しかし 一この方法も、広い面積を一度に施工すると、
樹脂モルタルの硬化収縮性が大きいため各所に亀裂を生
じたり、剥離し易くなり、かつ耐酸性や滑り止めの目的
が達成されなかつた。それ故その改良のために予め目地
を切り、樹脂モルタルライニングを行い、目地を後から
コーキング剤などで埋め込むようなことが行れている。
しかし、この場合、目地の耐薬品性が劣ることや、鉄板
やコンクリートと樹脂モルタルの熱膨張率の差異や、鉄
板のたわみ、コンクリートの経時的ヒビ割れが原因とな
り、樹脂モルタルライニング施工面に亀裂が起り易く、
かつ剥離や薬液、水分の浸透などにより、その耐久性が
短縮される場合が多かつた。更にコンクリート、モルタ
ル施工構造物においては、基材の硬化収縮によるヘアー
クラックや、.構造上の応力、歪による亀裂の発生によ
り表面被覆材はそれに抗しきれなくなり、基材と共にヘ
アークラック、亀裂を生ずることが散見された。However, with this method, if a large area is constructed at once,
Since the resin mortar has a large curing shrinkage, it tends to crack in various places and peel off easily, and the purpose of acid resistance and non-slip properties cannot be achieved. Therefore, in order to improve this, the joints are cut in advance, lined with resin mortar, and then the joints are filled in with caulking agent or the like.
However, in this case, cracks may occur on the resin mortar lining construction surface due to poor chemical resistance of the joints, differences in thermal expansion coefficients between the steel plate or concrete and resin mortar, deflection of the steel plate, and cracking of the concrete over time. is likely to occur,
Moreover, its durability was often shortened due to peeling, penetration of chemicals, moisture, etc. Furthermore, in concrete and mortar construction structures, hair cracks due to curing shrinkage of the base material, etc. Due to the occurrence of cracks due to structural stress and strain, the surface coating material was unable to withstand it, and hair cracks and fissures were occasionally observed to occur together with the base material.
そのため、特別に伸び率の大きい軟質ウレタンの塗布や
プラスチックやゴムシートの接着により亀裂−を生じな
いコンクリート防水施工法が開発されている。しかし、
塗布による方法は膜厚が薄く、又、流動性があるため、
流れ易く、凹凸の激しいコンクリート面などでは均一な
厚膜の施工が行えないこと、またシート防水施工法にお
いてはシー3卜の接着性やシートの貼合せ又は重ね合せ
面において、接着不良や完全な遮断効果を得にくいなど
の欠点が見られた。更に、鉄やアルミニウム製のタンク
、コンクリート貯水槽、排水溝など、高濃度の酸、アル
カ4リ、塩に接触する樹脂ライニングにおいても、金属
とライニング層との熱膨張、収縮の差異による熱ショッ
クおよび金属面の外的応力歪によるライニング層の亀裂
や剥離、あるいはコンクリート面における基材の亀裂に
よるライニング層の亀裂、剥離等の欠陥が生じていた。Therefore, concrete waterproofing construction methods that do not cause cracks have been developed by applying soft urethane with a special high elongation rate or adhering plastic or rubber sheets. but,
The coating method has a thin film and is fluid, so
It is difficult to apply a uniformly thick film on concrete surfaces that flow easily and are highly uneven, and in the sheet waterproofing method, there may be problems such as poor adhesion or complete failure due to the adhesion of the three sheets or the lamination or overlapping surfaces of the sheets. There were drawbacks such as difficulty in obtaining a blocking effect. Furthermore, even with resin linings that come into contact with highly concentrated acids, alkalis, and salts, such as iron or aluminum tanks, concrete water tanks, and drainage ditches, thermal shock occurs due to the difference in thermal expansion and contraction between the metal and the lining layer. Also, defects such as cracking or peeling of the lining layer due to external stress strain on the metal surface or cracking or peeling of the lining layer due to cracks in the base material on the concrete surface occurred.
本発明は前述の如き従来技術の欠点を改良することを目
的とするものである。The present invention aims to improve the drawbacks of the prior art as described above.
すなわち、水平構造の基材は勿論のこと、垂直面や天井
面に対して厚膜て均等な膜厚を有し、しかも耐衝撃性、
弾性、接着性、耐酸性、耐アルカリ性、硬度、引掻強度
、伸張率、復元性、耐歪性等にすぐれた、自己接着性、
弾性層を有する被覆施工法を提供しようとするものであ
る。本発明は、基材表面上に、(a)部分加硫ゴム10
〜5踵量%、粘着付与剤10〜5種量%および充填剤5
〜7腫量%からなる厚さ0.3〜3TWLの自己粘着
性テープを圧着し、ついで(b)FRPライニング、フ
レークライニング、レジンモルタルライニングの少くと
も一種を施すことを特徴とする自己接着性、弾性層を有
する被覆施工法に関する。In other words, it has a thick and uniform film thickness not only on horizontal substrates, but also on vertical surfaces and ceiling surfaces, and has good impact resistance.
Self-adhesive, with excellent elasticity, adhesion, acid resistance, alkali resistance, hardness, scratch strength, elongation, resilience, distortion resistance, etc.
The present invention aims to provide a coating construction method having an elastic layer. The present invention provides (a) partially vulcanized rubber 10 on the surface of the base material.
~5% heel weight, 10~5% tackifier and 5% filler
A self-adhesive property characterized by compressing a self-adhesive tape with a thickness of 0.3 to 3 TWL and having a volume of ~7%, and then (b) applying at least one of FRP lining, flake lining, and resin mortar lining. , relates to a coating construction method having an elastic layer.
本発明の施工法において、第一層目の自己粘着性テープ
に用いられるゴムとしては、天然ゴム、スチレン−ブタ
ジエンゴム、ニトリルゴム、ポリイソプレンゴム、ポリ
ブタジエン、エピクロルヒドリンゴム、クロロスルホン
化ポリエチレン、ブチルゴム、エチレン−プロピレンゴ
ム、エチレンープロピレンージエンゴム、ウレタンゴム
等が挙げられる。In the construction method of the present invention, the rubber used for the first layer of self-adhesive tape includes natural rubber, styrene-butadiene rubber, nitrile rubber, polyisoprene rubber, polybutadiene, epichlorohydrin rubber, chlorosulfonated polyethylene, butyl rubber, Examples include ethylene-propylene rubber, ethylene-propylene-diene rubber, and urethane rubber.
特に耐熱性、耐屈曲性、耐蒸気性、耐引裂性、耐ガス透
過性、耐オゾン性などの点からブチルゴム、エピクロル
ヒドリンゴム、エチレン−プロピレンゴム、ハイパロン
などが好ましい。未加硫の原料ゴムは硫黄、有機硫黄化
合物、有機過酸化物、金属酸化物、ポリアミン、ポリイ
ソシアネートなどの加硫剤や、必要に応じ、アルデヒド
−アミン反応生成物、ジチオカーバメート類、グアニジ
ン類、チウラム類などの加硫促進剤を用い常法により加
硫を行つて、部分加硫したゴムとする。本発明において
前記ゴムが未加硫であると、温度による塑性流動の依存
性が大きく、弾性や引張強度が低く、酸化による脆化が
早く、耐久性に乏しい。Particularly preferred are butyl rubber, epichlorohydrin rubber, ethylene-propylene rubber, hypalon, etc. from the viewpoint of heat resistance, bending resistance, steam resistance, tear resistance, gas permeability resistance, ozone resistance, and the like. Unvulcanized raw rubber is treated with vulcanizing agents such as sulfur, organic sulfur compounds, organic peroxides, metal oxides, polyamines, and polyisocyanates, and as necessary, aldehyde-amine reaction products, dithiocarbamates, and guanidines. Vulcanization is carried out by a conventional method using a vulcanization accelerator such as thiurams or the like to obtain a partially vulcanized rubber. In the present invention, if the rubber is unvulcanized, its plastic flow will be highly dependent on temperature, its elasticity and tensile strength will be low, it will quickly become brittle due to oxidation, and it will have poor durability.
一方、加硫が過多になると硬質となり、弾性や伸び率が
低下するので不適当となりそれ故、部分加硫にとゞめる
ことが必要である。On the other hand, excessive vulcanization becomes hard and reduces elasticity and elongation, making it unsuitable and therefore requiring only partial vulcanization.
最適加硫範囲は、使用するゴムの種類により異るが、引
張り強さの最高値を示すよりも伸長率が最高値を示す程
度の加硫が適し、伸び率は400〜1500%、引張強
度は0.5〜8k9/C7lであることが望ましい。な
お、酸素、オゾン、光、熱による変化や疲労による劣化
をなるべく少くする効果のある、アミン類、アミン−ア
ルデヒド反応物、アミン−ケトンb反応物、フェノール
類などの老化防止剤を加えることが望ましい。本発明に
於ける自己粘着性テープ中に含まれる部分加硫ゴムはテ
ープの全配合物に対し10〜5踵量%、好ましくは15
〜45重量%用いる。The optimal vulcanization range varies depending on the type of rubber used, but vulcanization that shows the maximum elongation is more suitable than the maximum tensile strength. is preferably 0.5 to 8k9/C7l. In addition, it is recommended to add anti-aging agents such as amines, amine-aldehyde reactants, amine-ketone b reactants, and phenols, which have the effect of minimizing changes due to oxygen, ozone, light, heat, and deterioration due to fatigue. desirable. The partially vulcanized rubber contained in the self-adhesive tape according to the invention is 10 to 5% by heel weight, preferably 15% by weight, based on the total formulation of the tape.
~45% by weight is used.
この範囲1より部分加硫ゴムが少いと、テープの伸びの
不足による切断や、弾性が不足して、本発明の意図する
諸目的を達成することができない。逆に多過すぎると、
基材に対する接着力やテープ同志の感圧自己接着性か低
下する。又、本発明における自己粘着性テープに使用さ
れる粘着付与剤としては、ポリブテン樹脂、テルペン樹
脂、ポリイソブチレン樹脂、エステル化ロジン、キシレ
ン樹脂、水添石油樹脂、などが用いられる。If the amount of partially vulcanized rubber is less than this range 1, the tape may be cut due to insufficient elongation or elasticity may be insufficient, making it impossible to achieve the objectives of the present invention. On the other hand, if there is too much
Adhesion to the base material and pressure-sensitive self-adhesion between tapes decrease. Further, as the tackifier used in the self-adhesive tape of the present invention, polybutene resin, terpene resin, polyisobutylene resin, esterified rosin, xylene resin, hydrogenated petroleum resin, etc. are used.
又、タールや鉱油などを併用することも出来る。該粘着
付与剤はテープ同志の継ぎ目や重ね合せ目を感圧粘着し
、一体化し隙間がなく、また経時的にテープ同志が剥れ
ることを無くすような自己接着性を与えるための必須成
分である。またこの成分により鉄やコンクリートなど被
施工基材に対し、特別な接着剤を予め施さなくても手動
ロールなどで押しつける圧力て強固に粘着する効果を示
すようになる。自己粘着性テープ全配合物中に占める該
粘着付与剤の量は、10〜印重量%、好ましくは、15
〜45重量%である。この使用量が前記範囲より少い場
合にはテープの自己感圧接着力か失われ、一方被施工基
材に対する粘着性が十分でなくなる。またこの使用量が
前記範囲より多くなり過ぎると、高温度における塑性流
動を起し、テープの保存中での変形流動や施工後の膜厚
変化が生じたり、上層に塗布する層にすれやしわを生ず
る原因になるので好ましくない。本発明において、自己
粘着性テープには、更に充填剤を含む。Furthermore, tar, mineral oil, etc. can also be used in combination. The tackifier is an essential component for providing pressure-sensitive adhesives to the seams and overlaps of tapes, creating a single unit with no gaps, and providing self-adhesive properties that prevent the tapes from peeling off over time. . In addition, this component allows the adhesive to firmly adhere to the base material to be applied, such as steel or concrete, by applying pressure using a hand roll or the like, without the need for applying a special adhesive in advance. The amount of said tackifier in the total formulation of the self-adhesive tape ranges from 10% to 15% by weight, preferably 15% by weight.
~45% by weight. If the amount used is less than the above range, the tape will lose its self-pressure-sensitive adhesive strength and will not have sufficient adhesion to the substrate to which it is applied. If the amount used is too much above the above range, plastic flow may occur at high temperatures, causing deformation and flow during storage of the tape, changes in film thickness after application, and rubbing or wrinkles in the upper layer. This is not preferable as it may cause In the present invention, the self-adhesive tape further includes a filler.
該充填剤としては、カーボンブラック、微粉末シリカ、
ケイ酸カルシウム、亜釦f(華、クレー、炭酸カルシウ
ム、炭酸マグネシウム、硫酸バリウム、タルク、カオリ
ンなどが用(゛られる。必要に応じて、チタン白、チタ
ンエロー、フタロシアニンブルー、フタロシアニングリ
ーン、キナクリドンレツドなど種々の無機および有機の
一般の着色顔料あるいはジンククロメート、ストロンチ
ウムクロメート、鉛丹、鉛酸カルシウムなど鉄やアルミ
ニウムに対する防錆顔料を加えることが出来る。該充填
剤の量はテープ全配合中5〜旬重量%、好ましくは10
〜印重量%てある。該充填剤が前記範囲より少いとテー
プが高温時に塑性流動を起し易く、また前記範囲より多
いと伸びや弾性などの物性が低下すると同時に感圧自己
接着性や基材に対する粘着力が低下するのて好ましくな
い。前記の如き諸成分からなる自己粘着性テープは、ロ
ールやパンバリーミキサーで素練し、熱ロールにかけた
後、カレングーや押出機により均一な厚さに調節して製
造され、離型紙の上に乗せ巻取つて保存される。As the filler, carbon black, fine powder silica,
Calcium silicate, clay, calcium carbonate, magnesium carbonate, barium sulfate, talc, kaolin, etc. are used. If necessary, titanium white, titanium yellow, phthalocyanine blue, phthalocyanine green, quinacridone red. Various inorganic and organic general coloring pigments such as zinc chromate, strontium chromate, red lead, calcium lead oxide, and other anticorrosion pigments for iron and aluminum can be added. Seasonal weight%, preferably 10
〜marked weight%. If the filler content is less than the above range, the tape is likely to undergo plastic flow at high temperatures, while if it is more than the above range, physical properties such as elongation and elasticity will decrease, as well as pressure-sensitive self-adhesion and adhesive strength to the substrate. I don't like it. A self-adhesive tape made of the various components described above is manufactured by masticating it with a roll or a Panbury mixer, applying it to a hot roll, adjusting it to a uniform thickness with a calender or extruder, and then applying it to a release paper. It is then rolled up and stored.
該テープの膜厚は、0.3WUTL〜3771771と
する。通常0.5〜1.57T11ftの間が実用的で
ある。尚、自己接着性テープを製造する際に、テープの
両面又は片面あるいは内部に補強材として無機又は有機
質繊維を使用することも可能てある。The film thickness of the tape is 0.3 WUTL to 3771771 mm. Usually, a value between 0.5 and 1.57 T11 ft is practical. Incidentally, when producing a self-adhesive tape, it is also possible to use inorganic or organic fibers as a reinforcing material on both sides or one side of the tape, or inside the tape.
例えは、クロスあるいは不織布としてガラス質のクロス
、チヨツプドストランドマツト、サーフエイスマット、
ビニロンあるいはポリプロピレンクロ・ス、カーボン繊
維クロスおよびマットあるいは合成樹脂の複合強化用不
織布〔例えば日本石油化学(株)製商品名日石ワリフ等
〕などが単独あるいは組合せて使用出来る。本発明にお
いて該テープの巾や長さは取扱い易フい様にまた施エエ
事基材の面積などに合せて自由に変形可能である。Examples of cloth or non-woven fabrics include glass cloth, chopped strand mat, surf ace mat,
Vinylon, polypropylene cloth, carbon fiber cloth, and composite reinforcing nonwoven fabrics of mat or synthetic resin (for example, Nisseki Warif manufactured by Nippon Petrochemicals Co., Ltd.) can be used alone or in combination. In the present invention, the width and length of the tape can be freely modified to facilitate handling and to suit the area of the substrate to be treated.
本発明で云う「FRPライニング」とは、無機または有
機質繊維クロスあるいは不織布等に種々の合成樹脂を塗
布、含浸させて得られる強化プラ5スチツクライニング
をいう。The "FRP lining" used in the present invention refers to reinforced plastic lining obtained by coating and impregnating various synthetic resins on inorganic or organic fiber cloth or nonwoven fabric.
前記無機または有機質繊維のクロスまたは不織布として
は、ガラスのクロス、チヨツプドスプランドマツト、サ
ーフエーシングマツトやビニロンあるいはポリプロピレ
ンクロス、カーボン繊維ク゛oロスおよびマット、ある
いは合成樹脂の複合強化用不織布〔例えば日本石油化学
(掬製商品名:日石ワリフなど〕が用いられる。Examples of the inorganic or organic fiber cloth or nonwoven fabric include glass cloth, chopped splint mat, surfacing mat, vinylon or polypropylene cloth, carbon fiber cloth and mat, or composite reinforcing nonwoven fabric of synthetic resin. For example, Nippon Petrochemical (product name: Nisseki Warif, etc.) is used.
この中ではガラスクロスやガラスチヨツプドストランド
マツトが物性と経済性の面から代表的てかつ好ましいも
のてある。前記種々の素材繊維の組合せや、クロスとマ
ットの組合せは目的によつて自由に採用することがてき
る。Among these, glass cloth and glass chopped strand mat are representative and preferable from the viewpoint of physical properties and economical efficiency. Combinations of the various material fibers and combinations of cloth and mat can be freely adopted depending on the purpose.
本発明における上記無機または有機繊維のクロスまたは
不織布に塗布、含浸させる樹脂としては、アミンまたは
ポリアミド硬化性エポキシ樹脂、ポリオ−ルーポリイソ
シアネート樹脂、不飽和ポリエステル樹脂、ビニルエス
テル樹脂、フラン樹脂など通常市販されているものが用
いられる。これらの樹脂は室温で硬化すること、また塗
布容易で含浸が十分行われること、溶剤など揮発成分が
全く無いかあるいは殆んどなく、厚膜の硬化膜が得易く
、クロスやマットを十分に包含し目痩が小さいこと、お
よび硬化膜の硬度が高く、外圧や衝撃に抗し得る強化層
となることが必要である。このため、特にポリオ−ルー
ポリイソシアネート樹脂、不飽和ポリエステルやビニル
エステル樹脂は常温で低粘度て含浸性、施工性がよく、
適当な硬化触媒を加えれは速硬化性て工期短縮によく、
また特にビニルエステル樹脂、エポキシ樹脂、イソフタ
ル酸系不飽和ポリエステル樹脂、ビスフェノール系不飽
和ポリエステル樹脂は耐酸、耐アルカリ性、耐水性、耐
湿性、耐オゾン性などの性質も優れているのて好適であ
る。本発明て云う「フレークライニング」とは、ガlラ
スフレーク、グラファイトフレーク、マイカフレーク等
に各種合成樹脂を混練したコンパウンドから得られるラ
イニングをいう。In the present invention, the resin to be coated and impregnated on the inorganic or organic fiber cloth or nonwoven fabric is commonly commercially available, such as amine or polyamide curable epoxy resin, polyol-polyisocyanate resin, unsaturated polyester resin, vinyl ester resin, furan resin, etc. The one listed will be used. These resins cure at room temperature, are easy to apply, are well impregnated, have no or almost no volatile components such as solvents, are easy to obtain thick cured films, and are easily coated with cloth or matte. It is necessary for the curing film to have a small amount of wrinkles and to have high hardness, so that it becomes a reinforcing layer that can withstand external pressure and impact. For this reason, polyol-polyisocyanate resins, unsaturated polyesters, and vinyl ester resins have low viscosity at room temperature and have good impregnating and workability.
Adding an appropriate curing catalyst will cure quickly and shorten the construction period.
Furthermore, vinyl ester resins, epoxy resins, isophthalic acid-based unsaturated polyester resins, and bisphenol-based unsaturated polyester resins are particularly suitable as they have excellent properties such as acid resistance, alkali resistance, water resistance, moisture resistance, and ozone resistance. . The term "flake lining" used in the present invention refers to lining obtained from a compound obtained by kneading glass flakes, graphite flakes, mica flakes, etc. with various synthetic resins.
該合成樹脂としては、前記FRPライニングで用いられ
る樹脂、例えばエポキシ樹脂、不飽和ポ3りエステル樹
脂、ウレタン樹脂、フラン樹脂、ビニルエステル樹脂な
ど通常市販されているものが好適に使用される。As the synthetic resin, commercially available resins used in the FRP lining, such as epoxy resins, unsaturated polyester resins, urethane resins, furan resins, and vinyl ester resins, are preferably used.
更に、本発明で云う「レジンモルタルライニング」とは
、例えばエポキシ樹脂、不飽和ポリエス3テル樹脂、ウ
レタン樹脂、フラン樹脂、ビニルエステル樹脂等に、ケ
イ砂などを混合して得られる樹脂モルタルライニングを
いう。Furthermore, "resin mortar lining" as used in the present invention refers to a resin mortar lining obtained by mixing silica sand or the like with, for example, epoxy resin, unsaturated polyester 3-ter resin, urethane resin, furan resin, vinyl ester resin, etc. say.
次に本発明における施工発明の詳細な説明する。Next, the construction invention according to the present invention will be explained in detail.
”′まず基材てある金属やコンクリート面に対し、部
分加硫コム、粘着付与剤および充填剤から成る自己粘着
性テーーブ(離型紙を使用して巻取つたもの)を貼付け
る。自己粘着性テープは離型紙の上からローラーで押え
つけることによつて、基材に容易にかつ確実に均一な厚
さで接着する。その後離型紙を剥がす。該テープの継ぎ
合せ部分は、テープの端末を間隙を開けず隣接させ、合
せ目の上に離型紙をおいて、ロールなどで押えつけると
、テープの弾性による変形と自己接着性により、合せ目
はテープ同志接合し一体化する。``First, a self-adhesive tape (rolled using release paper) consisting of a partially vulcanized comb, tackifier, and filler is applied to the base metal or concrete surface.Self-adhesive By pressing the tape onto the release paper with a roller, it easily and reliably adheres to the base material with a uniform thickness.Then, the release paper is peeled off.The spliced part of the tape is attached to the end of the tape. When the tapes are placed adjacent to each other with no gap between them, a release paper is placed over the seam, and the tape is pressed down with a roll, etc., the seams become joined and integrated due to the tape's elastic deformation and self-adhesive properties.
かくして通常のプラスチックテープや、ゴムシートなど
の場合のように特別フな接着剤や加熱熔着などを特に必
要とせず、しかも接合面の接着不良による透水性防止効
果の低下や接合面での膜厚の不均一性もない、平滑完全
不透過層が得られる。本発明に於けるテープの継ぎ合せ
法の別の態様・としては、先に自己粘着性テープを圧着
し、離型紙を剥した層上に次のテープをいくらか重ね合
せて圧着する方法がある。In this way, unlike ordinary plastic tapes or rubber sheets, there is no need for special adhesives or heat welding, and there is no need to use special adhesives or heat welding, and there is no need for poor adhesion on the bonding surfaces, which can reduce the water permeability prevention effect or prevent membrane formation on the bonding surfaces. A smooth, completely impermeable layer with no non-uniformity in thickness is obtained. Another embodiment of the tape splicing method according to the present invention is a method in which a self-adhesive tape is first pressure-bonded, and then the next tape is partially overlapped and pressure-bonded on the layer from which the release paper has been removed.
この方法によつても完全一体化した不透過層が構成出来
る。なお基材には予め、塗料が塗布されていてもそれが
確実に基材に固着していれば、その上に前記テープの施
工を行つても支障はない。A completely integrated impermeable layer can also be constructed by this method. Note that even if a paint has been applied to the base material in advance, as long as it is firmly adhered to the base material, there is no problem even if the tape is applied thereon.
次に前記粘着性テープ上に1FRPライニング、2フレ
ークライニング、3レジンモルタルライニングを施す。Next, 1 FRP lining, 2 flake lining, and 3 resin mortar lining are applied on the adhesive tape.
例えば前記FRPライニングの場合、テープ施工面の上
に無機又は有機質繊維のクロスまたはマットを貼付ける
。これはクロスまたはマットをテープの上に乗せロール
で圧着する方法による。この場合テープ表面は粘着性が
強いので特に接着剤を施す必要はなく、クロスやマット
とテープの接触面は、クロスやマットが幾分テープ内部
に入り込んだ様な状態になる。またクロスやマットはテ
ープの粘着性遮断層となり、ロール圧着などの作業の困
難性はない。ついで、テープ上に浮出しているクロスや
マットに対して樹脂の塗布、含浸を行う。For example, in the case of the FRP lining, an inorganic or organic fiber cloth or mat is pasted on the tape application surface. This is done by placing a cloth or mat on top of the tape and pressing it with a roll. In this case, since the surface of the tape is highly adhesive, there is no need to apply any particular adhesive, and the contact surface between the cloth or mat and the tape will be in a state where the cloth or mat has somewhat penetrated into the tape. In addition, the cloth or mat acts as an adhesive barrier layer for the tape, and there is no difficulty in work such as roll crimping. Next, a resin is applied and impregnated onto the cloth or mat that stands out on the tape.
例えは不飽和ポリエステル樹脂などを流展又はスプレー
し、脱泡ロールにより繊維への含浸と膜中に含まれる気
泡を除去する。又、前記と同様にしてガラスフレーク、
グラファイトフレーク、マイカフレークなどを用いてフ
レークライニングを行うことも出来る。更に前記自己粘
着性テ−プーhに、前述したレジンモルタルをコテ等に
より塗布することも出来る。For example, an unsaturated polyester resin or the like is spread or sprayed, and a defoaming roll is used to impregnate the fibers and remove air bubbles contained in the film. Also, in the same manner as above, glass flakes,
Flake lining can also be performed using graphite flakes, mica flakes, etc. Furthermore, the above-mentioned resin mortar can also be applied to the self-adhesive tape h using a trowel or the like.
尚、本発明において「FRPライニング、フレークライ
ニング、レジンモルタルライニングの少くとも一種を施
す」とは、前記自己粘着性テープ上に、(1)FRPラ
イニングを一層もしくは二層以上施す、(2)フレーク
ライニングを一層もしくは二層以上施す、(3)レジン
モルタルライニングを一層もしくは二層以上施す、(4
)FRPライニングの上にフレークライニング及び/又
はレジンモルタルライニングを施す、(5)フレークラ
イニングの上にFRPライニング及び/又はレジンモル
タルライニンクを施す、等の各種の組合せを包含する。In the present invention, "applying at least one of FRP lining, flake lining, and resin mortar lining" means (1) applying one or more layers of FRP lining on the self-adhesive tape, (2) applying flake lining. Applying one or more layers of lining, (3) Applying one or more layers of resin mortar lining, (4
) Applying flake lining and/or resin mortar lining on FRP lining, (5) Applying FRP lining and/or resin mortar lining on flake lining, etc.
特に本発明においては、自己粘着性テープ上にFRPラ
イニングを施すことが一番好ましい。かくすることによ
り抗張力、引張強度、圧縮強度などの強大な強化プラス
チック層が形成され、粘着テープ層との複合により強化
プラスチックの欠点である基材への接着不良による剥離
や熱ショック或は歪および耐クリープ性による亀裂や疲
労による強度低下の防止がてき、耐衝撃性が著しく向上
される。加えてクッション性、耐震性などの特性が得ら
れる。尚、本発明の施工法により得られた被覆層上に更
に通常の常温乾燥性の油性あるいは合成樹脂塗料を塗布
して表面の着色あるいは保護を行つたり、適度の粒径の
ジルコンサンド、アルミナ、ボーキサイト粒子を散布し
て滑り止め効果をもたせたり、ウレタンエラストマー等
を貼着して防水性を付与したりすることも可能である。Particularly in the present invention, it is most preferable to provide FRP lining on the self-adhesive tape. In this way, a reinforced plastic layer with strong tensile strength, tensile strength, and compressive strength is formed, and when combined with the adhesive tape layer, the disadvantages of reinforced plastics such as peeling due to poor adhesion to the base material, thermal shock, distortion, and Creep resistance prevents deterioration in strength due to cracks and fatigue, and impact resistance is significantly improved. In addition, properties such as cushioning properties and earthquake resistance can be obtained. Furthermore, on the coating layer obtained by the construction method of the present invention, a normal room temperature drying oil-based or synthetic resin paint may be applied to color or protect the surface, or zircon sand or alumina of appropriate particle size may be applied. It is also possible to provide an anti-slip effect by scattering bauxite particles, or to provide waterproofness by attaching urethane elastomer or the like.
前記の如くして得られた本発明の被覆層は、耐衝撃性、
弾性、接着性、耐酸性、耐アルカリ性、硬度、引掻強度
、伸張率、復元性、耐歪性等のすぐれたものである。The coating layer of the present invention obtained as described above has impact resistance,
It has excellent elasticity, adhesiveness, acid resistance, alkali resistance, hardness, scratch strength, elongation, restorability, distortion resistance, etc.
次に前記本発明の施工法により構成される自己接着性と
弾性層を有する積層被覆膜の一断面の概要を第1図に示
す。Next, FIG. 1 shows an outline of a cross section of a laminated coating film having a self-adhesive and elastic layer constructed by the construction method of the present invention.
第1図において、1は基材であり、例えは軟鋼、ステン
レス、アルミニウム、銅などの金属またはコンクリート
、モルタル、スレートなどの無機構造材てある。In FIG. 1, reference numeral 1 denotes a base material, such as a metal such as mild steel, stainless steel, aluminum, or copper, or an inorganic structural material such as concrete, mortar, or slate.
2は自己粘着性テープである。2 is a self-adhesive tape.
すなわち部分加硫したコムに粘着付与剤や充填剤を配合
した自己粘着性を有し弾性、伸ひ率の優れたテープの層
である。3は繊維クロスまたはマットを2に圧着し、か
つ常温硬化性樹脂を塗布、含浸させた硬化膜てある。In other words, it is a tape layer made of a partially vulcanized comb mixed with a tackifier and a filler, which has self-adhesive properties and has excellent elasticity and elongation. 3 is a cured film obtained by pressing a fiber cloth or mat onto 2 and coating and impregnating it with a room-temperature curable resin.
4は通常の塗料またはライニング層(FRP)フレーク
あるいはレジンモルタルライニング層)である。4 is a normal paint or lining layer (FRP flakes or resin mortar lining layer).
本発明の施工法を適用出来る分野としては、化学、石油
プラント、貯槽、水処理、廃気処埋設備等の耐薬品ライ
ニング;海洋や港湾施設の長期防食;鉄、コンクリート
における剥離やヒビ割れのない耐酸床仕上げ;歩道橋、
飛行甲板などの滑り止め舗装;コンクリート製プール、
廃水貯槽、建築構造物などの耐亀裂、洩水、防水仕上げ
;ライニング鋼管の接合部の現場防食施工;長大橋のメ
イン,ケーブル、ハンガーケーブルなどのワイヤーロー
ブの防食ラッピング施工等巾広い分野に、巾広い適用が
可能である。従つて、上記羅列例に限定されるものでな
く、当業者が容易に想到しうる適用例に同等に使用可能
であることは論をまたない。以下本発明の詳細な説明例
により示す。Fields to which the construction method of the present invention can be applied include chemical-resistant linings for chemical and petroleum plants, storage tanks, water treatment, waste gas disposal equipment, etc.; long-term corrosion protection for marine and port facilities; and peeling and cracking in steel and concrete. No acid-resistant floor finishes; pedestrian bridges;
Anti-slip pavement for flight decks, etc.; concrete pools;
For a wide range of applications, such as crack-proof, leak-proof and waterproof finishing for wastewater storage tanks, building structures, etc.; on-site anti-corrosion work for joints of lining steel pipes; anti-corrosion wrapping work for wire lobes such as main cables and hanger cables for long bridges, etc. A wide range of applications is possible. Therefore, it goes without saying that the present invention is not limited to the examples listed above, and can equally be used in other applications that can be easily conceived by those skilled in the art. The present invention will be illustrated below with detailed examples.
実施例に記載する「部」又は「%」は夫々「重量部」又
は「重量%」をもつて示す。実施例1
部分加硫コムと粘着性付与剤および充填剤からなる自己
接着性、弾性を有するテープは第1表に示す配合により
ニーダーで均一に分散した後、押出機により巾10−、
厚さ1−て押出し離型紙の上に乗せ巻取り、適宜一定の
巾に裁断した。"Parts" and "%" described in Examples are shown as "parts by weight" and "% by weight," respectively. Example 1 A self-adhesive and elastic tape consisting of a partially vulcanized comb, a tackifier, and a filler was uniformly dispersed in a kneader according to the formulation shown in Table 1, and then made into a tape having a width of 10 mm and a width of 10 mm by an extruder.
It was extruded to a thickness of 1 mm, placed on release paper, rolled up, and cut into appropriate widths.
第1表の組成から成るテープを夫々巾10077Z77
1、長さ300Twt)厚さ5m77Iのスレート板の
片面に全面1にわたつて貼着し、剥型紙の上をローラー
で2〜3回押えた後、剥型紙を剥した。得られたテープ
の表面は非常に粘着性が強かつた。該テープの上にガラ
スチヨツプドストランドマツトを2枚重ね、ローラーで
3〜4回押えた後、硬化剤を加えたビスフェノール系不
飽和ポリエステル樹脂をチヨツブドストランドマツトが
完全に含浸するようにロール刷毛で塗り広げ、脱泡ロー
ルで気泡を除いて室温で硬化させた。いずれも2〜3時
間て硬化し積層硬化層の表面は硬く、粘着性がない状態
になつた。Each tape having the composition shown in Table 1 has a width of 10077Z77.
1. Length: 300 Twt) It was pasted over the entire surface on one side of a slate board with a thickness of 5 m and 77 mm, and after pressing the top of the release paper with a roller 2 to 3 times, the release paper was peeled off. The surface of the resulting tape was very sticky. Layer two pieces of glass chopped strand mat on top of the tape, press it down 3 to 4 times with a roller, and then press the tape so that the chopped strand mat is completely impregnated with the bisphenol-based unsaturated polyester resin to which a hardening agent has been added. It was spread on the surface with a roll brush, air bubbles were removed with a defoaming roll, and the mixture was cured at room temperature. All cured in 2 to 3 hours, and the surface of the laminated cured layer was hard and non-tacky.
この硬化層の上にエポキシ樹脂白色塗料〔シェル化学(
キわ製商品名エピコート1001に白色顔料を混合した
主剤に硬化剤としてポリアミド樹脂を加えた塗料〕を2
回塗りし、室温て硬化させて比較試験に供した。*’(
試験片A)一方、最初の自己接着性弾性テープ貼付けを
省いた他は同様にして得られた試験片(試験片B)、自
己接着弾性テープの代りにガラスチヨツプドマツトを4
層に増加した試験片(試験片C)、エポキシ樹脂塗料の
みを塗装した試験片(試験片D)本発明のテープNO.
l〜5のみ貼付けた試験片(試験片E)および全く被覆
施工を行わないスレート板基材(試験片F)を比較とし
て加えた。On top of this hardened layer, apply an epoxy resin white paint [Shell Chemical Co., Ltd.
2. A paint made by adding polyamide resin as a curing agent to the main ingredient, which is made by mixing Kiwa's product name Epicoat 1001 with a white pigment.
It was coated several times and cured at room temperature before being subjected to a comparative test. *'(
Test piece A) On the other hand, a test piece (test piece B) obtained in the same manner except that the first application of the self-adhesive elastic tape was omitted, and a glass chopped mat was used instead of the self-adhesive elastic tape.
A test piece with increased layers (test piece C), a test piece coated with only epoxy resin paint (test piece D), tape of the present invention No.
A test piece to which only samples 1 to 5 were pasted (test piece E) and a slate board base material to which no coating was applied (test piece F) were added for comparison.
試験結果を第2表に示す。尚テープの種類は5種類ある
がいずれのものも同様の結果であつた。第2表の試験結
果より明らかに本積層被覆施工皮膜は強靭てあり接着性
、弾性、耐衝撃性、防水、耐薬品性が優れ、基材の物理
的並に化学的保護作用が顕著であることが判る。L−ー
ーーニーーー 〜−ーーー −ー[(注)試験方法
(ハ 指を表面に押しつけて粘着、非粘
(2) 鉛筆硬度試,験による。The test results are shown in Table 2. Although there were five types of tapes, all of them gave similar results. From the test results in Table 2, it is clear that this laminated coating film is strong and has excellent adhesion, elasticity, impact resistance, waterproofing, and chemical resistance, and has a remarkable physical and chemical protective effect on the base material. I understand that. L-------------[(Note) Test method (C) Adhesive, non-stick by pressing your finger against the surface (2) Pencil hardness test, based on the test.
(3) 引掻試験器(荷重100V)によ 。(3) Using a scratch tester (load 100V).
を判定。実施例21前記第1表に記載されている各組成
によつて、厚さIwr!nおよび2TWLのテープを各
々作成し、巾100−、長さ500Trrm)厚さ57
7rmのスレート板を垂直にして貼付け、その上にガラ
スローピングクロスを一層貼り、ローラーにより圧着し
、硬化剤を加.えたイソフタル酸系不飽和ポリエステル
樹脂をロール刷毛により塗布し脱泡ロールを使用して含
浸、脱泡を行つた。Determine. Example 21 Depending on each composition listed in Table 1 above, the thickness Iwr! n and 2TWL tapes were made respectively, width 100-, length 500Trrm) thickness 57
A 7rm slate board was pasted vertically, a layer of glass roping cloth was pasted on top of it, it was crimped with a roller, and a hardening agent was added. The obtained isophthalic acid-based unsaturated polyester resin was applied with a roll brush, and impregnated and defoamed using a defoaming roll.
この積層被覆膜は約1.時間て硬化した。該硬化層の上
にアクリル・ウレタン樹脂塗料を2回塗布し、室温硬化
して試験に共し;た。一方比較例としてポリエステル−
ジアミン・グリコール硬化型ウレタンエラストマー〔大
日本インキ化学工業(掬製商品名:パンデツクス〕を前
記と同様に垂直に立てたスレート板に刷毛やロール刷毛
、コテなどにより出来るだけ厚く塗布するようにしたが
垂れ下り易くスレート面の膜厚は上部で約30ミクロン
、中程で50〜60ミクロン、下部で100〜200ミ
クロンと相対的には薄く、又膜厚は不均一であり、ガラ
スローピングクロスの貼付けではローピングクロスのズ
リ下りがあり施工は困難を極め又樹脂を含浸させた後の
状態は、ローピングクロスの網目の樹脂の充填が悪くク
ロス目が著しく浮き上つた状態になつた。This laminated coating film is about 1. It hardened over time. An acrylic/urethane resin paint was applied twice on the cured layer, cured at room temperature, and used for testing. On the other hand, as a comparative example, polyester
The diamine glycol curing type urethane elastomer [Dainippon Ink & Chemicals Co., Ltd. (Kiki-made product name: Pandex) was applied as thickly as possible to the vertically erected slate board using a brush, roll brush, trowel, etc. in the same manner as above. It is easy to sag, and the film thickness on the slate surface is relatively thin, about 30 microns at the top, 50 to 60 microns in the middle, and 100 to 200 microns at the bottom, and the film thickness is uneven, so it is difficult to attach glass roping cloth. In this case, the construction was extremely difficult as the roping cloth slipped down, and after impregnation with resin, the mesh of the roping cloth was poorly filled with resin and the cross stitches stood out significantly.
エポキシ樹脂塗料を塗布して得られた試験片を実施例1
と同様な性 フ能試験を行つたが、前記本発明に係る施
工皮膜は実施例1と同等の極めて優れた性能を示した。
しかし比較例の積層皮膜は弾性、や機械的強度に乏しく
実施例1の第2表比較例Dと類似する性能しか示さなか
つた。 つ本実施例により本発明の均一な弾性層を形成
する施工の特長が明らかである。Example 1 A test piece obtained by applying epoxy resin paint
A performance test similar to that of Example 1 was conducted, and the applied coating according to the present invention exhibited extremely excellent performance equivalent to that of Example 1.
However, the laminated film of the comparative example lacked elasticity and mechanical strength and exhibited performance similar to that of Comparative Example D in Table 2 of Example 1. This example makes clear the advantages of the construction of forming a uniform elastic layer according to the present invention.
実施例3
コンクリート製U字型排水溝の目地切部(目地の間隔3
〜6=)に、前記第1表に記載されたNO..4の組成
による厚さ0.8、巾100T!Rlftのテープを圧
着し、その上にビニロンクロス2枚を圧着し、硬化剤と
してトリエチルアミンを加えた液状エポキシ樹脂〔シェ
ル化学(掬製商品名:エビコート828〕を塗布、脱泡
ロール含浸、脱泡し24時間硬化させた後、実施例1に
記載したエポキシ樹脂塗料を1回塗りし、10日間乾燥
させた。Example 3 Joint cutting part of concrete U-shaped drainage ditch (joint spacing 3
~6=), the NO. listed in Table 1 above. .. 4 composition, thickness 0.8, width 100T! Crimp Rlft tape, crimp 2 vinylon cloths on top of it, apply liquid epoxy resin [Shell Chemical (product name: Ebicoat 828 made by Kiki)] containing triethylamine as a hardening agent, impregnate defoaming roll, defoaming. After curing for 24 hours, one coat of the epoxy resin paint described in Example 1 was applied and allowed to dry for 10 days.
又、コンクリート製貯水槽に0.5〜1m77tの巾で
クラックを生じている部分に前記同様の施工を施した。
かくして得られたコンクリートの目地やクラック部の積
層被覆部には割れを生ぜず完全にシールされた状態が維
持された。自己接着性弾性テープを用いす硬化剤を混合
した液状エポキシ樹脂とビニロンクロスを用い、ビニロ
ンクロスを3乃至5層積層し、エポキシ樹脂塗料を塗装
して得られた目地やコンクリートひび割れ部分は施工後
3〜10日後には表面に目地、ひび割れに沿つた0.1
〜0.2wLの細長い割れが1〜3筋発生し、防水シー
ルは不完全であることが外見・上からもはつきり認めら
れた。Further, the same construction as described above was carried out on a part of the concrete water tank where a crack had formed with a width of 0.5 to 1 m77 t.
The thus obtained laminated coating at joints and cracks in the concrete remained completely sealed without cracking. Use self-adhesive elastic tape. Use liquid epoxy resin mixed with a hardening agent and vinylon cloth. Laminate 3 to 5 layers of vinylon cloth, and paint joints and concrete cracks with epoxy resin paint after construction. After 3 to 10 days, 0.1
One to three elongated cracks of ~0.2 wL occurred, and it was clearly recognized from the outside that the waterproof seal was incomplete.
又、エポキシ樹脂塗料を6回塗り重ねたが、目地やコン
クリートのひひ割れは、阻止することが出来なかつた。
実施例4部分加硫ブチルゴム25部、テルペン樹脂2揶
、フジンククロメート2盲、炭酸カルンウム3瑯、微粉
シリカ5部からなる厚さ1wrm)巾75−の離型紙を
はさんだ連続巻取りテープを作成し、これを巾75Tr
Un)長さ30()Mm)厚さ1.6TfU!lのサン
ドブラストした軟鋼板に圧着し、剥型紙を剥力化た後、
ガラスフチヨツプドストランドマツト2枚を圧着した。Also, although epoxy resin paint was applied six times, cracks in the joints and concrete could not be prevented.
Example 4 A continuous winding tape was prepared by sandwiching a release paper (thickness: 1 wrm) with a width of 75 cm, consisting of 25 parts of partially vulcanized butyl rubber, 2 parts of terpene resin, 2 parts of Fujinku chromate, 3 parts of carunium carbonate, and 5 parts of finely divided silica. Create this with a width of 75Tr
Un) Length 30 () Mm) Thickness 1.6TfU! After pressing on a sandblasted mild steel plate and making the release paper peelable,
Two pieces of glass-edge hopped strand mats were crimped together.
ついでメチルエチルケトンパーオキサイドを硬化剤とし
て加えたビニルエステル樹脂を含浸させ硬化した後、同
じ樹脂でガラスサーフエージングマツトを含浸積層し、
常温硬化させて試験片を作成した。(試験片G)一方比
較のため同一の大きさのサンドブラスト軟鋼板に上記と
同じ樹脂でガラスチヨツプドストランドマツト2層とサ
ーフエーシングマツトー層を積層して常温硬化させて試
験片(試験片H)を,*作成した。Then, after impregnating and curing a vinyl ester resin containing methyl ethyl ketone peroxide as a hardening agent, a glass surfaging mat was impregnated and laminated with the same resin.
A test piece was prepared by curing at room temperature. (Test piece G) On the other hand, for comparison, two layers of glass chopped strand matte and a layer of surfacing matte were laminated with the same resin as above on a sandblasted mild steel plate of the same size and cured at room temperature. Test piece H) was created.
又、前記試験片Hに於いてガラスチヨツプドストランド
マツトを4枚重ねた積層試験片(試験片I)を作成し各
々試験に供した。試験結果を第3表に示す。In addition, a laminated test piece (test piece I) was prepared by stacking four glass chopped strand mats of the above test piece H, and each was subjected to the test. The test results are shown in Table 3.
実施例5
巾257Trm)長さ125−、厚さ1.6TWLのサ
ンドブラストした軟鋼板を巾25TrrWLの面て2枚
つき合せ1組とし、実施例4の試験片C.H.Iと夫々
同じ施工を行い試験片G,,H,,l,とし、7日間硬
化後引張試験器〔東洋測器(掬テンシロンUTM−1/
5000型〕によりロードセル500kg、引張速度1
.5Wr1Tt/分測定温度25゜Cで伸張率を測定し
た。Example 5 Two sandblasted mild steel plates with a width of 257Trm) and a thickness of 1.6TWL with a width of 25TrWL were put together to form a set, and the test specimen C. H. Test specimens G, , H, , l were prepared in the same manner as I, and after curing for 7 days, they were tested using a tensile tester [Toyo Sokki (Kiki Tensilon UTM-1/
5000 type] with a load cell of 500 kg and a tensile speed of 1
.. The elongation rate was measured at 5Wr1Tt/min and a measurement temperature of 25°C.
測定結果を第4表に示す。The measurement results are shown in Table 4.
住(1)引張試験器により伸張率以下の値で引張り、張
力を零にした時、基材軟鋼板の間隔の復元性を調べた。(1) Using a tensile tester, the material was pulled at a value less than the elongation rate, and when the tension was reduced to zero, the restorability of the spacing between the base mild steel plates was investigated.
実施例6
巾35Tr$L)長さ150TWt)厚さ1.6wLの
サンドブラストした軟硬板に実施例4の試験片G)H,
,Iと夫々同じ施工を行い、試験片G2,H。Example 6 Test piece of Example 4 G) H,
, I. The same construction was carried out as for test specimens G2 and H.
,I。とし7日間硬化後、引張試験器により曲け強度の
測定法を利用して積層皮膜に亀裂を生するまての歪を測
定した。測定条件はスパン距離IOC)TWI)ロード
セル500k9、曲げ速度1.5Twt/分てあり、測
定結果は第5表に示した。実施例7
厚さ1.6wuftのサンドブラストした軟鋼板に実施
例4に記載した厚さ1TfU−FLのテープとガラスチ
ヨツプドストランドマツト2層をビニルエステル樹脂て
積層した硬化皮膜の上に、カラスフレーク〔旭ファイバ
ーグラス(+わ製商品名:グラスロンフレークGF−C
8〕3園とビニルエステル樹脂を混合したフレークコン
パウンドに硬化剤としてメチルエチルケトンパーオキサ
イドを混合し、コテにより厚さ1wrmで2回塗り重ね
、計2TWLの厚さのフレークコンパウンド層を積層し
た。,I. After curing for 7 days, the strain required to cause cracks in the laminated film was measured using a bending strength measuring method using a tensile tester. The measurement conditions were a span distance IOC) TWI) load cell 500k9, and a bending speed of 1.5 Twt/min, and the measurement results are shown in Table 5. Example 7 A hardened film was prepared by laminating the 1TfU-FL tape described in Example 4 and two layers of glass chopped strand mat using vinyl ester resin on a sandblasted mild steel plate with a thickness of 1.6 wuft. Crow flakes [Asahi fiberglass (+ made of wood) Product name: Glassron flakes GF-C
8] Methyl ethyl ketone peroxide was mixed as a hardening agent into a flake compound prepared by mixing three types of resin and vinyl ester resin, and the mixture was coated twice with a trowel to a thickness of 1 wrm to form a flake compound layer with a total thickness of 2 TWL.
(試験片J)一方比較としてサンドブラストした軟鋼板
にビニルエステル樹脂を下塗した後、上記と同じフレ−
クコンパウンドを1−ずつ2回積層した試験片(試験片
K)および3回積層した試験片(試験片L)を作成した
。 *これらの試験片について実施例4,5,6と同様
な試験を行つた。(Test piece J) As a comparison, a sandblasted mild steel plate was primed with vinyl ester resin, and then the same frame as above was used.
A test piece (test piece K) in which the compound was laminated twice (test piece K) and a test piece in which the compound was laminated three times (test piece L) were prepared. *The same tests as in Examples 4, 5, and 6 were conducted on these test pieces.
試験結果を第6表に示す。(注)l)デュポン式衝撃試
,験(径l/4〃、ィ其の他は前記表と同一の試験法に
よつた。実施例8
実施例4に於いて積層基材として巾50(YrfUn)
長さ300m77I)厚さ2−の透明ガラス板を用いテ
ープを隣接して圧着し、離型紙の上からローラーてテー
プ隣接面を押え付け試験片Aと同様な積層施工を行い、
ガラスの面の反対(積層していない面)からテープの間
隙の有無を拡大鏡で調べた。The test results are shown in Table 6. (Note) l) DuPont type impact test, test (diameter l/4〃, other than that, the same test method as in the above table was followed. YrfUn)
Length: 300 m (77 I) Using transparent glass plates with a thickness of 2-2, the tapes were crimped adjacent to each other, and the adjacent surface of the tape was pressed down using a roller over the release paper to perform lamination construction in the same manner as for test specimen A.
The presence or absence of gaps between the tapes was examined using a magnifying glass from the opposite side of the glass (the non-laminated side).
最初テープの隣接距離が、1TrrjTL程度離れてい
ても隣接面の上からの離型紙を置いてのロール圧着やチ
ョップ及びクロスの貼着時のロール圧着により隣接テー
プの弾性歪と自己接着性によソー体化し、全く間隔がな
く、気泡も残らず境界のない完全一体(眼500y.高
さ40m)による。(の皮膜になつていることが認めら
れた。Even if the adjacent tapes are initially separated by about 1TrrjTL, the elastic strain and self-adhesiveness of the adjacent tapes will be affected by the roll crimping with a release paper placed on the adjacent surface or the roll crimping during chop and cross application. It is completely integrated with no gaps, no air bubbles, and no boundaries (eye 500y, height 40m). (It was observed that it had become a film of
またテープを1〜10TjUrL重ね合せて圧着した場
合も全く異状が見られなかつた。Further, no abnormality was observed when 1 to 10 TjUrL of tapes were overlapped and pressed together.
実施例9
前記実施例1の第1表NO.3の組成による自己接着性
、弾性テープを用い実施例4の施工要領により積層した
。Example 9 Table 1 No. of Example 1 above. The self-adhesive elastic tape having the composition No. 3 was laminated according to the construction procedure of Example No. 4.
但し、ガラスチヨツプドストランドマツトの含浸積層用
樹脂としては、酸硬化型フラン樹脂〔日立化成(株)製
商品名;ヒタフラン302〕を用いた。その結果は第7
表に示した。第7表中試験片Mは本発明てあり、試験片
N及ひoは前記施工において自己接着性、弾性テープを
使用しないものである。±
実施例10
部分加硫ブチルゴム30、ロンジエステル15部、タル
ク508卜、コロイグルシリカ5部の組成の厚さ1.5
TW1、巾150T$L自己接着性弾性テープを作り、
巾300薦、長さ1000WLぃ厚さ5薦のスレート板
の表面全面にテープを隣接して圧着し、ついでガラスチ
ヨツプドストランドマツトを一枚圧着し、硬化剤を加え
たビスフェノール系不飽和ポリエステル樹脂を含浸、硬
化させた。However, as the resin for impregnating and laminating the glass chopped strand mat, an acid-curing furan resin (trade name: Hitafuran 302, manufactured by Hitachi Chemical Co., Ltd.) was used. The result is the 7th
Shown in the table. Test piece M in Table 7 is of the present invention, and test pieces N and O are self-adhesive and do not use elastic tape in the construction. ± Example 10 Thickness 1.5 with composition of partially vulcanized butyl rubber 30, longiester 15 parts, talc 508 ml, coroiglu silica 5 parts
TW1, width 150T$L self-adhesive elastic tape was made.
Tape is crimped adjacent to the entire surface of a slate board with a width of 300 mm, length of 1000 WL, and a thickness of 5 mm, and then a piece of glass chopped strand mat is crimped, and a bisphenol-based unsaturated material with a hardening agent added thereto. Impregnated with polyester resin and cured.
更にその上に液状エポキシ樹脂100部に硬化剤として
ポリアミド樹脂とトリエチレンテトラミンを加えた混合
物15部及び粗砕珪砂85部を混合したレジンモルタル
コンパウンドを5Tfr!TLの厚さでコラ塗して硬化
させた。この積層被覆膜は歩行や車の走行に対し滑り止
め効果があると共に歩行時弾性があり、且スレート板に
応力をかけてもレジンモルタル面に亀裂を生じなかつた
。又径1/4“、荷重1kg、高さ50cmの衝撃試験
(表面及ひ裏面衝撃)でも亀裂を生じなかつた。一方自
己接着性、弾性テープの貼付けを省略した積層被覆層は
滑り止め効果は同じであつたが、庫゛歩行時硬い感じが
強く、スレート板に応力をかけると亀裂を生じ、応力の
くりかえしにより被覆レジンモルタルが剥離した。Furthermore, a resin mortar compound made by mixing 100 parts of liquid epoxy resin with 15 parts of a mixture of polyamide resin and triethylenetetramine as curing agents and 85 parts of coarsely crushed silica sand was added at 5 Tfr! I coated it with a TL thickness and cured it. This laminated coating film had an anti-slip effect when walking or driving a car, and was elastic when walking, and did not cause cracks on the resin mortar surface even when stress was applied to the slate board. Also, no cracks occurred in impact tests (front and back impact) with a diameter of 1/4", a load of 1 kg, and a height of 50 cm.On the other hand, the laminated coating layer, which is self-adhesive and does not require the attachment of elastic tape, has no anti-slip effect. Although it was the same, it felt very hard when walking in the warehouse, cracks appeared when stress was applied to the slate board, and the covering resin mortar peeled off due to repeated stress.
又前記同一条件の衝撃試験では衝撃部がスレート基材と
共に亀裂を生じた。実施例11
第1表の組処NO.5からなる自己接着性弾性テープを
片面サンドブラスト板に貼付け、その上にコテでガラス
フレークコンパウンド 〔大日本塗料(株)製商品名レ
ジライニングFC−30〕を施工した後、脱泡ロールを
用いて脱泡を行い、平滑にし、膜厚2T!Rmに仕上げ
た。In addition, in the impact test under the same conditions as described above, the impact part cracked together with the slate base material. Example 11 Assembling process NO. in Table 1. A self-adhesive elastic tape consisting of No. 5 was attached to a single-sided sandblast board, and a glass flake compound [trade name: Resi Lining FC-30, manufactured by Dainippon Toyo Co., Ltd.] was applied with a trowel on top of the tape, and then a defoaming roll was used to apply Degassed and smoothed to a film thickness of 2T! Finished in Rm.
その後常温硬化させた。It was then cured at room temperature.
(試験片P)別に自己接着性弾性テープの貼付けを省き
、ガラスフレークコンパウンド2TrUT1のライニン
グを行つた試験片(試験片Q)、及び同様にガラスフレ
ークコンパウンド3rf0nのライニングを行つた試験
片(試験片R)を作成した。(Test piece P) A test piece lined with glass flake compound 2TrUT1 without attaching self-adhesive elastic tape (test piece Q), and a test piece similarly lined with glass flake compound 3rf0n (test piece R) was created.
これらの試験片の耐衝撃性、伸張率、曲け歪を測定した
結果を、第8表に示した。上記の如く本発明の方法によ
るものは、優れた耐衝撃性、伸張率、曲げ歪を有してい
た。The results of measuring the impact resistance, elongation rate, and bending strain of these test pieces are shown in Table 8. As described above, the material produced by the method of the present invention had excellent impact resistance, elongation rate, and bending strain.
実施例12
実施例11と同様にして自己接着性弾性テープを貼付け
た後、硬化剤、促進剤を加えたビニルエステル樹脂10
臨に、シリカ粉末10娼、粗砕珪砂30部を混合したレ
ジンモルタルコンパウンドを厚さ3Tf0!lになるよ
うライニングした後、常温硬化させた。Example 12 After applying a self-adhesive elastic tape in the same manner as in Example 11, vinyl ester resin 10 was added with a curing agent and an accelerator.
First, a resin mortar compound mixed with 10 parts of silica powder and 30 parts of coarsely crushed silica sand was applied to a thickness of 3Tf0! After lining it so that it had a diameter of 1, it was cured at room temperature.
(試験片S)別にレジンモルタルコンパウンドのみを厚
さ3TWLにライニングした試験片を得た。(試験片T
)上記表より明らかな如く本発明の方法により得られた
製品は優れた性能を有するものであつた。(Test piece S) Separately, a test piece was obtained which was lined with only a resin mortar compound to a thickness of 3TWL. (Test piece T
) As is clear from the above table, the products obtained by the method of the present invention had excellent performance.
第1図は本発明の施工法により得られた被覆層の一例の
断面図てある。
1は基材、2は自己粘着性テープ層、3はFRPライニ
ング層、4は通常の塗料、フレークライニング、レジン
モルタルライニング等の層を示す。FIG. 1 is a sectional view of an example of a coating layer obtained by the construction method of the present invention. 1 is a base material, 2 is a self-adhesive tape layer, 3 is an FRP lining layer, and 4 is a layer such as ordinary paint, flake lining, resin mortar lining, etc.
Claims (1)
%、粘着付与剤10〜50重量%および充填剤5〜70
重量%からなる厚さ0.3〜3mmの自己粘着性テープ
を圧着し、ついで(b)FRPライニング、フレークラ
イニング、レジンモルタルライニングの少くとも一種を
施すことを特徴とする自己接着性弾性層を有する被覆施
工法。 2 (b)工程においてFRPライニングを施した後フ
レークライニングを施すことを特徴とする特許請求の範
囲第1項記載の自己接着性弾性層を有する被覆施工法。 3 (b)工程においてFRPライニングを施した後レ
ジンモルタルライニングを施すことを特徴とする特許請
求の範囲第1項記載の自己接着性弾性層を有する被覆施
工法。4 FRPライニングは、無機または有機質繊維
のクロスまたは不織布と常温硬化性のエポキシ樹脂、不
飽和ポリエステル樹脂、ウレタン樹脂、ビニルエステル
樹脂、フラン樹脂の少くとも1種とから得られたライニ
ングである特許請求の範囲第1項、第2項又は第3項記
載の自己接着性弾性層を有する被覆施工法。 5 フレークライニングはガラスフレーク、グラファイ
トフレーク、マイカフレークと常温硬化性のエポキシ樹
脂、不飽和ポリエステル樹脂、ウレタン樹脂、ビニルエ
ステル樹脂、フラン樹脂の少くとも1種とから得られた
ライニングである特許請求の範囲第1項又は第2項記載
の自己接着性弾性層を有する被覆施工法。[Scope of Claims] 1. On the surface of the base material, (a) 10 to 50% by weight of partially vulcanized rubber, 10 to 50% by weight of tackifier, and 5 to 70% of filler.
A self-adhesive elastic layer is formed by pressing a self-adhesive tape with a thickness of 0.3 to 3 mm consisting of % by weight, and then (b) applying at least one of FRP lining, flake lining, and resin mortar lining. Covering construction method. 2. The coating construction method having a self-adhesive elastic layer according to claim 1, wherein in step (b), FRP lining is applied and then flake lining is applied. 3. The coating construction method having a self-adhesive elastic layer according to claim 1, characterized in that in step (b), FRP lining is applied and then resin mortar lining is applied. 4. The patent claim that the FRP lining is a lining obtained from an inorganic or organic fiber cloth or nonwoven fabric and at least one of a room temperature-curable epoxy resin, an unsaturated polyester resin, a urethane resin, a vinyl ester resin, and a furan resin. A coating construction method having a self-adhesive elastic layer according to item 1, item 2, or item 3. 5. The flake lining is a lining obtained from glass flakes, graphite flakes, mica flakes and at least one of room temperature curable epoxy resin, unsaturated polyester resin, urethane resin, vinyl ester resin, and furan resin. A coating construction method having a self-adhesive elastic layer according to scope 1 or 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8427276A JPS6048230B2 (en) | 1976-07-15 | 1976-07-15 | Coating method with self-adhesive elastic layer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8427276A JPS6048230B2 (en) | 1976-07-15 | 1976-07-15 | Coating method with self-adhesive elastic layer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5313687A JPS5313687A (en) | 1978-02-07 |
| JPS6048230B2 true JPS6048230B2 (en) | 1985-10-25 |
Family
ID=13825809
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8427276A Expired JPS6048230B2 (en) | 1976-07-15 | 1976-07-15 | Coating method with self-adhesive elastic layer |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6048230B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0815207B2 (en) * | 1986-02-04 | 1996-02-14 | 富士通株式会社 | Semiconductor memory device |
| JPS63230323A (en) * | 1987-03-19 | 1988-09-26 | Toyota Motor Corp | Bonding method of structural member |
| JP3502318B2 (en) * | 2000-01-28 | 2004-03-02 | ジャパンコンポジット株式会社 | Composite covering structure for waterproofing and its construction method |
-
1976
- 1976-07-15 JP JP8427276A patent/JPS6048230B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5313687A (en) | 1978-02-07 |
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