SE448549B - Vid rumstemperatur herdande limkomposition for forbindning av metallmaterial - Google Patents
Vid rumstemperatur herdande limkomposition for forbindning av metallmaterialInfo
- Publication number
- SE448549B SE448549B SE7903533A SE7903533A SE448549B SE 448549 B SE448549 B SE 448549B SE 7903533 A SE7903533 A SE 7903533A SE 7903533 A SE7903533 A SE 7903533A SE 448549 B SE448549 B SE 448549B
- Authority
- SE
- Sweden
- Prior art keywords
- weight
- group
- monomer
- polymerizable
- adhesive
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 161
- 239000007769 metal material Substances 0.000 title claims description 3
- 239000003292 glue Substances 0.000 title description 12
- 239000000853 adhesive Substances 0.000 claims description 204
- 230000001070 adhesive effect Effects 0.000 claims description 204
- 239000000178 monomer Substances 0.000 claims description 76
- 150000001875 compounds Chemical class 0.000 claims description 44
- 229920000642 polymer Polymers 0.000 claims description 37
- 239000003638 chemical reducing agent Substances 0.000 claims description 34
- 239000007800 oxidant agent Substances 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 33
- 229910052698 phosphorus Inorganic materials 0.000 claims description 33
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 32
- 239000011574 phosphorus Substances 0.000 claims description 32
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- -1 hydroxyalkyl ester Chemical class 0.000 claims description 25
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 20
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 19
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 16
- 238000006116 polymerization reaction Methods 0.000 claims description 11
- 239000000047 product Substances 0.000 claims description 11
- 150000003512 tertiary amines Chemical class 0.000 claims description 11
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 10
- 150000001336 alkenes Chemical class 0.000 claims description 10
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- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 9
- 230000007704 transition Effects 0.000 claims description 9
- 238000012644 addition polymerization Methods 0.000 claims description 8
- 125000005907 alkyl ester group Chemical group 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 8
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 150000005215 alkyl ethers Chemical class 0.000 claims description 6
- 229920001519 homopolymer Polymers 0.000 claims description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 5
- 230000036961 partial effect Effects 0.000 claims description 5
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 229920002857 polybutadiene Polymers 0.000 claims description 4
- 239000005062 Polybutadiene Substances 0.000 claims description 3
- 239000011145 styrene acrylonitrile resin Substances 0.000 claims description 3
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 claims description 2
- KCAMXZBMXVIIQN-UHFFFAOYSA-N octan-3-yl 2-methylprop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C(C)=C KCAMXZBMXVIIQN-UHFFFAOYSA-N 0.000 claims description 2
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 claims description 2
- 239000013536 elastomeric material Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims 1
- 239000012766 organic filler Substances 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 description 35
- 239000002184 metal Substances 0.000 description 35
- 239000000758 substrate Substances 0.000 description 34
- 150000003254 radicals Chemical class 0.000 description 27
- 238000000034 method Methods 0.000 description 22
- 238000005304 joining Methods 0.000 description 21
- 238000012360 testing method Methods 0.000 description 21
- 229910000831 Steel Inorganic materials 0.000 description 18
- 229910052782 aluminium Inorganic materials 0.000 description 18
- 239000010959 steel Substances 0.000 description 18
- 239000002253 acid Substances 0.000 description 17
- 238000004026 adhesive bonding Methods 0.000 description 16
- 229920001971 elastomer Polymers 0.000 description 16
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 15
- 229940102838 methylmethacrylate Drugs 0.000 description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 14
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 13
- 238000002203 pretreatment Methods 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 239000000806 elastomer Substances 0.000 description 12
- 229920005862 polyol Polymers 0.000 description 12
- 150000003077 polyols Chemical class 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000012190 activator Substances 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 230000007613 environmental effect Effects 0.000 description 10
- 229920001228 polyisocyanate Polymers 0.000 description 10
- 239000005056 polyisocyanate Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000010276 construction Methods 0.000 description 9
- 229920003023 plastic Polymers 0.000 description 9
- 239000004033 plastic Substances 0.000 description 9
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 9
- 239000004342 Benzoyl peroxide Substances 0.000 description 8
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 8
- 235000019400 benzoyl peroxide Nutrition 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 229920001084 poly(chloroprene) Polymers 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 238000003860 storage Methods 0.000 description 8
- 239000003981 vehicle Substances 0.000 description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 7
- 229920002681 hypalon Polymers 0.000 description 7
- 230000000977 initiatory effect Effects 0.000 description 7
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 239000007859 condensation product Chemical class 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 239000011976 maleic acid Substances 0.000 description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- 101100459319 Arabidopsis thaliana VIII-2 gene Proteins 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 230000002411 adverse Effects 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 239000002131 composite material Substances 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000010452 phosphate Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 5
- 230000000379 polymerizing effect Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
- 101100132433 Arabidopsis thaliana VIII-1 gene Proteins 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- 239000004840 adhesive resin Substances 0.000 description 4
- 229920006223 adhesive resin Polymers 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
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- 239000000126 substance Substances 0.000 description 4
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- 235000020679 tap water Nutrition 0.000 description 4
- JFZVSHAMRZPOPA-UHFFFAOYSA-N 1-[n-(2-hydroxypropyl)-4-methylanilino]propan-2-ol Chemical compound CC(O)CN(CC(C)O)C1=CC=C(C)C=C1 JFZVSHAMRZPOPA-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 239000004709 Chlorinated polyethylene Substances 0.000 description 3
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- 239000011230 binding agent Substances 0.000 description 3
- BIOOACNPATUQFW-UHFFFAOYSA-N calcium;dioxido(dioxo)molybdenum Chemical compound [Ca+2].[O-][Mo]([O-])(=O)=O BIOOACNPATUQFW-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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- 239000011787 zinc oxide Substances 0.000 description 3
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 3
- 229910000165 zinc phosphate Inorganic materials 0.000 description 3
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- 101001053395 Arabidopsis thaliana Acid beta-fructofuranosidase 4, vacuolar Proteins 0.000 description 2
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- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
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- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 2
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- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
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- YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
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- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
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- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000012041 precatalyst Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
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- 238000011012 sanitization Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- KIEOKOFEPABQKJ-UHFFFAOYSA-N sodium dichromate Chemical compound [Na+].[Na+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KIEOKOFEPABQKJ-UHFFFAOYSA-N 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940113165 trimethylolpropane Drugs 0.000 description 1
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- QRCJOCOSPZMDJY-UHFFFAOYSA-N valnoctamide Chemical compound CCC(C)C(CC)C(N)=O QRCJOCOSPZMDJY-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- XAEWLETZEZXLHR-UHFFFAOYSA-N zinc;dioxido(dioxo)molybdenum Chemical compound [Zn+2].[O-][Mo]([O-])(=O)=O XAEWLETZEZXLHR-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
- C09J5/02—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving pretreatment of the surfaces to be joined
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
- C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2400/00—Presence of inorganic and organic materials
- C09J2400/10—Presence of inorganic materials
- C09J2400/16—Metal
- C09J2400/166—Metal in the pretreated surface to be joined
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/899,621 US4223115A (en) | 1978-04-24 | 1978-04-24 | Structural adhesive formulations |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE7903533L SE7903533L (sv) | 1979-10-25 |
| SE448549B true SE448549B (sv) | 1987-03-02 |
Family
ID=25411303
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7903533A SE448549B (sv) | 1978-04-24 | 1979-04-23 | Vid rumstemperatur herdande limkomposition for forbindning av metallmaterial |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4223115A (en, 2012) |
| JP (1) | JPS54141826A (en, 2012) |
| AT (1) | AT376233B (en, 2012) |
| BE (1) | BE875813A (en, 2012) |
| CA (1) | CA1138149A (en, 2012) |
| CH (1) | CH666693A5 (en, 2012) |
| DE (1) | DE2916537C2 (en, 2012) |
| DK (1) | DK167679A (en, 2012) |
| FR (3) | FR2438080A1 (en, 2012) |
| GB (1) | GB2019415B (en, 2012) |
| IT (1) | IT1112576B (en, 2012) |
| NL (1) | NL187817C (en, 2012) |
| NO (1) | NO154523C (en, 2012) |
| SE (1) | SE448549B (en, 2012) |
| ZA (1) | ZA791288B (en, 2012) |
Families Citing this family (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1207944A (en) * | 1980-09-15 | 1986-07-15 | Denis J. Zalucha | Fast curing phosphate modified anaerobic composition |
| US4322509A (en) * | 1980-10-03 | 1982-03-30 | Lord Corporation | Fast curing phosphate modified anaerobic adhesive compositions |
| JPS5915468A (ja) * | 1982-07-16 | 1984-01-26 | Kuraray Co Ltd | 接着剤 |
| US4452944A (en) * | 1982-02-11 | 1984-06-05 | Lord Corporation | Structural adhesive formulations |
| US4467071A (en) * | 1982-09-13 | 1984-08-21 | Lord Corporation | Epoxy modified structural adhesives having improved heat resistance |
| JPS59172567A (ja) * | 1983-03-22 | 1984-09-29 | Okura Ind Co Ltd | 変性二液型接着剤組成物 |
| JPS60120774A (ja) * | 1983-12-05 | 1985-06-28 | Okura Ind Co Ltd | 接着性と保存安定性に優れた二液型アクリル系接着剤 |
| US4703089A (en) * | 1984-04-10 | 1987-10-27 | Damico Dennis J | Structural adhesive formulations |
| CA1231085A (en) * | 1984-05-29 | 1988-01-05 | Denis J. Zalucha | Structural adhesive formulations |
| DE3431369A1 (de) * | 1984-08-25 | 1986-03-06 | Keck Chimie S.A., Ingwiller | Modifizierter polyurethan-klebstoff |
| US5028661A (en) * | 1986-10-14 | 1991-07-02 | Loctite Corporation | Adhesion promoters for thiolene adhesive formulations |
| DE3727112A1 (de) * | 1987-08-14 | 1989-02-23 | Basf Ag | Waessrige beschichtungsstoffe auf basis von sekundaerdispersionen carboxylgruppen enthaltender copolymerisate von acrylsaeure- oder methacrylsaeureestern |
| US4788235A (en) * | 1987-11-23 | 1988-11-29 | Minnesota Mining And Manufacturing Company | Phosphite modified epoxy resin |
| US5096962A (en) * | 1990-11-29 | 1992-03-17 | Lord Corporation | Acrylic adhesive compositions |
| JP2642554B2 (ja) * | 1991-12-27 | 1997-08-20 | 電気化学工業株式会社 | 接着剤組成物 |
| US5385958A (en) * | 1993-03-05 | 1995-01-31 | Dymax Corporation | Activator formulation and composition utilizing same |
| TW414713B (en) | 1994-05-12 | 2000-12-11 | Dentsply Gmbh | Fluoride releasing liquid dental primer product and method |
| BR9607693A (pt) * | 1995-03-20 | 1999-11-30 | Dymax Corp | Fórmula, processo e aparelho para encapsulação |
| CA2243573A1 (en) * | 1996-04-15 | 1997-10-23 | Lord Corporation | Free radical polymerizable compositions including para-halogenated aniline derivatives |
| JP3412430B2 (ja) * | 1996-10-28 | 2003-06-03 | 株式会社スリーボンド | ねじ部材などに用いられるプレコート型接着剤組成物及びこれを用いたプレコート螺合部材 |
| ID20459A (id) | 1997-06-24 | 1998-12-24 | Denki Kagaku Kogyo Kk | Komposisi resin yang bisa mengawetkan, komposisi perekat, produk dan susunan yang diawetkan |
| US6288190B1 (en) * | 1997-09-20 | 2001-09-11 | Roehm Gmbh | Materials which can be thermally coated with a polymerizable component |
| US6153719A (en) * | 1998-02-04 | 2000-11-28 | Lord Corporation | Thiol-cured epoxy composition |
| BR9911157A (pt) * | 1998-06-12 | 2001-03-27 | Lord Corp | Formulações de adesivo |
| US6559257B2 (en) * | 1998-06-12 | 2003-05-06 | Lord Corporation | Adhesive formulations |
| US6225408B1 (en) * | 1998-06-12 | 2001-05-01 | Lord Corporation | Adhesive formulations |
| IE980948A1 (en) * | 1998-11-16 | 2000-05-17 | Loctite R & D Ltd | Method of bonding Aluminium Substrates with Anaerobic Sealants to form a Seal |
| US6313257B1 (en) | 1999-03-23 | 2001-11-06 | Lord Corporation | Poly (mercaptopropylaryl) curatives |
| US6762249B1 (en) * | 1999-08-25 | 2004-07-13 | Hitachi Chemical Company, Ltd. | Wiring-connecting material and process for producing circuit board with the same |
| US6632872B1 (en) | 2000-09-19 | 2003-10-14 | 3M Innovative Properties Company | Adhesive compositions including self-assembling molecules, adhesives, articles, and methods |
| KR100518317B1 (ko) * | 2000-12-22 | 2005-10-04 | 주식회사 포스코 | 인산히드록시알킬아크릴레이트를 함유하는 전기강판표면처리용 유무기 복합형 코팅액의 유기재 수지 조성물 |
| EP1239015A1 (en) * | 2001-03-08 | 2002-09-11 | Sika AG, vorm. Kaspar Winkler & Co. | Easy to manufacture meth (acrylic) adhesive compositions |
| US6433091B1 (en) | 2001-05-10 | 2002-08-13 | Henkel Loctite Corporation | Adhesive composition |
| US6596379B2 (en) | 2001-05-24 | 2003-07-22 | Exxonmobil Oil Corporation | Polymers stabilized by water-soluble, cationic, amino-functional polymer, and plastic film coated with same |
| US20050014901A1 (en) | 2001-07-10 | 2005-01-20 | Ips Corporation | Adhesive compositions for bonding and filling large assemblies |
| US6630555B2 (en) * | 2001-11-06 | 2003-10-07 | Lord Corporation | Internally blocked organoborate initiators and adhesives therefrom |
| US6921454B2 (en) | 2001-11-27 | 2005-07-26 | Henkel Corporation | Elastomer toughened radiation curable adhesives |
| US6730411B1 (en) | 2002-02-07 | 2004-05-04 | Illinois Tool Works Inc. | Two-part structural adhesive systems and laminates incorporating the same |
| US6893722B2 (en) * | 2002-04-29 | 2005-05-17 | Exxonmobil Oil Corporation | Cationic, amino-functional, adhesion-promoting polymer for curable inks and other plastic film coatings, and plastic film comprising such polymer |
| US7195818B2 (en) | 2002-05-01 | 2007-03-27 | Exxonmobil Oil Corporation | Sealable multi-layer opaque film |
| US6989416B2 (en) * | 2002-05-07 | 2006-01-24 | Sika Technology Ag | Methacrylate structural adhesive |
| US20040105994A1 (en) * | 2002-12-03 | 2004-06-03 | Pang-Chia Lu | Thermoplastic film structures with a low melting point outer layer |
| US20040229990A1 (en) * | 2003-05-16 | 2004-11-18 | Lord Corporation | Acrylic structural adhesive having improved T-peel strength |
| US20040242817A1 (en) * | 2003-05-29 | 2004-12-02 | Lord Corporation | Internally coordinated organoboranes |
| US7060327B2 (en) * | 2003-11-13 | 2006-06-13 | Henkel Corporation | Corrosion protective methacrylate adhesives for galvanized steel and other metals |
| EP1732707B1 (en) | 2004-03-19 | 2015-04-22 | Commonwealth Scientific and Industrial Research Organisation | Activation method |
| US20050244216A1 (en) * | 2004-04-29 | 2005-11-03 | Michael Magraw | Coupler |
| BRPI0606574A2 (pt) | 2005-01-21 | 2017-06-27 | Commw Scient Ind Res Org | métodos de ativação de um revestimento orgânico e de preparação de um tratamento de ativação, substrato revestido e tratamento de ativação para um revestimento orgânico |
| KR20080009725A (ko) * | 2005-05-19 | 2008-01-29 | 로드코포레이션 | 주위온도 경화성 보호 실란트 |
| EP2363443B1 (en) * | 2005-12-15 | 2020-11-18 | Huntsman Advanced Materials Licensing (Switzerland) GmbH | Multiphase acrylic adhesives |
| US20070155899A1 (en) * | 2005-12-21 | 2007-07-05 | Ips Corporation | Elastic methacrylate compositions |
| US20070155879A1 (en) * | 2005-12-22 | 2007-07-05 | Ips Corporation | Adhesive compositions for bonding metals |
| CN101502188B (zh) * | 2006-07-21 | 2011-03-23 | 日立化成工业株式会社 | 电路连接材料、电路部件的连接结构及电路部件的连接方法 |
| WO2008014466A2 (en) | 2006-07-28 | 2008-01-31 | Lord Corporation | Dual cure adhesive formulations |
| US20080305345A1 (en) * | 2007-06-06 | 2008-12-11 | Peter William Uhlianuk | Protective coating composition for a metal substrate and a process for coating same |
| US20080305270A1 (en) * | 2007-06-06 | 2008-12-11 | Peter William Uhlianuk | Protective coating composition and a process for applying same |
| FR2928931B1 (fr) * | 2008-03-21 | 2011-03-25 | Jacret | Composition pour adhesif structural |
| EP2177553A1 (de) | 2008-10-17 | 2010-04-21 | Sika Technology AG | Radikalisch härtbare Zusammensetzungen mit reduzierter Weichmacheraufnahme |
| US20100113674A1 (en) * | 2008-10-31 | 2010-05-06 | Strand Richard M | Methacrylate adhesive |
| WO2010088648A2 (en) | 2009-02-02 | 2010-08-05 | Lord Corporation | Structural adhesives containing maleimide terminated polyimides |
| US7932323B1 (en) * | 2009-11-04 | 2011-04-26 | Equistar Chemicals, Lp | Polyolefin-based adhesives having improved oxidative stability |
| GB201005444D0 (en) * | 2010-03-31 | 2010-05-19 | 3M Innovative Properties Co | Epoxy adhesive compositions comprising an adhesion promoter |
| DE102011014731A1 (de) * | 2011-03-22 | 2012-09-27 | Stüwa Konrad Stükerjürgen GmbH | Brunnenfiltersegment |
| JP5701446B2 (ja) | 2011-03-29 | 2015-04-15 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 動的加硫された熱可塑性エラストマー積層 |
| DE102011088123A1 (de) | 2011-12-09 | 2013-06-13 | Henkel Ag & Co. Kgaa | Verfahren zum stoffschlüssigen Verbinden von Kunststoff-Rohren |
| US8859098B2 (en) * | 2012-05-18 | 2014-10-14 | Lord Corporation | Acrylic adhesion promoters |
| EP2877544A1 (en) | 2012-07-25 | 2015-06-03 | LORD Corporation | Improved post-vulcanization bonding |
| BR112016021419B1 (pt) | 2014-03-19 | 2021-06-22 | Lord Corporation | Composição curável |
| CN108350127B (zh) | 2015-11-03 | 2021-07-06 | 洛德公司 | 粘性快速发展的弹性体粘合剂 |
| US10759979B2 (en) | 2017-02-22 | 2020-09-01 | Lg Chem, Ltd. | Adhesive composition |
| KR102157352B1 (ko) | 2017-05-02 | 2020-09-17 | 주식회사 엘지화학 | 이액형 접착제 조성물 |
| KR102136705B1 (ko) | 2017-06-02 | 2020-07-22 | 주식회사 엘지화학 | 이액형 접착제 조성물 |
| JP7343506B2 (ja) * | 2017-09-12 | 2023-09-12 | ディディピー スペシャルティ エレクトロニック マテリアルズ ユーエス，エルエルシー | 接着剤調合物 |
| WO2019123885A1 (ja) | 2017-12-18 | 2019-06-27 | 株式会社スリーボンド | 接着積層鋼板用ラジカル重合性接着剤組成物、接着積層体、モータおよび接着積層体の製造方法 |
| WO2019130612A1 (en) * | 2017-12-28 | 2019-07-04 | Nitto Denko Corporation | Method for producing glass unit and pressure-sensitive adhesive sheet |
| FR3084370B1 (fr) | 2018-07-24 | 2021-03-05 | Jacret | Composition pour adhesif structural |
| US20210301183A1 (en) | 2020-03-24 | 2021-09-30 | Illinois Tool Works Inc. | Low surface energy accelerated bonding adhesive formulation and process for the use thereof |
| US20230086092A1 (en) * | 2021-09-17 | 2023-03-23 | Z Technologies Corporation | Solvent reducable urethane coating |
| KR20240093470A (ko) * | 2021-11-01 | 2024-06-24 | 가부시끼가이샤 쓰리본드 | 혐기 경화성 조성물 |
| EP4540296A1 (en) | 2022-06-17 | 2025-04-23 | Henkel AG & Co. KGaA | Two component (2k) curable adhesive composition |
| EP4481913A1 (en) | 2023-06-20 | 2024-12-25 | Henkel AG & Co. KGaA | Electronics assembly having electrochemically debondable components |
| CN117343564A (zh) * | 2023-09-06 | 2024-01-05 | 潍柴动力股份有限公司 | 一种铸渗涂料及其制备方法、带有铸渗层的进气道 |
| WO2025093205A1 (en) | 2023-10-31 | 2025-05-08 | Henkel Ag & Co. Kgaa | Two component (2k) curable and debondable adhesive composition |
| EP4566808A1 (en) | 2023-12-06 | 2025-06-11 | Henkel AG & Co. KGaA | Bonded structure comprising an electrochemically debondable adhesive |
| EP4567085A1 (en) | 2023-12-08 | 2025-06-11 | Henkel AG & Co. KGaA | Electrochemically debondable adhesive film |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1123419B (de) * | 1960-09-27 | 1962-02-08 | Degussa | Verfahren zum Verkleben von Metallen |
| US3160618A (en) * | 1961-11-03 | 1964-12-08 | Monsanto Co | Molecular weight regulation in polymerization of vinylidene monomers using acid phosphates as regulators |
| NL124155C (en, 2012) * | 1965-07-23 | |||
| JPS5310636B1 (en, 2012) * | 1971-07-01 | 1978-04-14 | ||
| US3845009A (en) * | 1972-02-03 | 1974-10-29 | Johnson & Johnson | Cement compositions employing novel methacrylate monomer |
| US3970505A (en) * | 1973-01-15 | 1976-07-20 | Loctite Corporation | Anaerobic compositions and surface activator therefor |
| US3984500A (en) * | 1974-01-08 | 1976-10-05 | Ford Motor Company | Radiation polymerizable coating composition containing an unsaturated phosphoric ester |
| JPS5713594B2 (en, 2012) * | 1974-06-05 | 1982-03-18 | ||
| JPS51132234A (en) * | 1975-04-21 | 1976-11-17 | Suriibondo:Kk | An anaerobic adhesive composition |
| US3994764A (en) * | 1975-06-13 | 1976-11-30 | Pratt & Lambert, Inc. | Adhesive compositions |
| US4081308A (en) * | 1977-07-27 | 1978-03-28 | National Starch And Chemical Corporation | Rapid curing two part adhesives |
-
1978
- 1978-04-24 US US05/899,621 patent/US4223115A/en not_active Expired - Lifetime
-
1979
- 1979-03-19 ZA ZA791288A patent/ZA791288B/xx unknown
- 1979-03-27 CA CA000324223A patent/CA1138149A/en not_active Expired
- 1979-04-20 NO NO791332A patent/NO154523C/no unknown
- 1979-04-23 SE SE7903533A patent/SE448549B/sv not_active IP Right Cessation
- 1979-04-23 FR FR7910200A patent/FR2438080A1/fr active Granted
- 1979-04-24 DE DE2916537A patent/DE2916537C2/de not_active Expired
- 1979-04-24 BE BE0/194802A patent/BE875813A/xx not_active IP Right Cessation
- 1979-04-24 DK DK167679A patent/DK167679A/da not_active IP Right Cessation
- 1979-04-24 CH CH3839/79A patent/CH666693A5/de not_active IP Right Cessation
- 1979-04-24 IT IT22123/79A patent/IT1112576B/it active
- 1979-04-24 NL NLAANVRAGE7903233,A patent/NL187817C/xx not_active IP Right Cessation
- 1979-04-24 AT AT0307379A patent/AT376233B/de not_active IP Right Cessation
- 1979-04-24 GB GB7914182A patent/GB2019415B/en not_active Expired
- 1979-04-24 JP JP5074879A patent/JPS54141826A/ja active Granted
-
1980
- 1980-01-09 FR FR8000394A patent/FR2438081A1/fr active Granted
- 1980-01-09 FR FR8000393A patent/FR2438077A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54141826A (en) | 1979-11-05 |
| ZA791288B (en) | 1980-05-28 |
| US4223115A (en) | 1980-09-16 |
| NO154523B (no) | 1986-06-30 |
| FR2438077B1 (en, 2012) | 1985-03-01 |
| BE875813A (fr) | 1979-10-24 |
| CA1138149A (en) | 1982-12-21 |
| IT7922123A0 (it) | 1979-04-24 |
| FR2438077A1 (fr) | 1980-04-30 |
| IT1112576B (it) | 1986-01-20 |
| NL187817C (nl) | 1992-01-16 |
| FR2438080B1 (en, 2012) | 1984-11-16 |
| ATA307379A (de) | 1984-03-15 |
| AT376233B (de) | 1984-10-25 |
| CH666693A5 (de) | 1988-08-15 |
| GB2019415A (en) | 1979-10-31 |
| DE2916537C2 (de) | 1986-02-20 |
| JPH039155B2 (en, 2012) | 1991-02-07 |
| FR2438081A1 (fr) | 1980-04-30 |
| FR2438080A1 (fr) | 1980-04-30 |
| NL7903233A (nl) | 1979-10-26 |
| FR2438081B1 (en, 2012) | 1983-11-04 |
| SE7903533L (sv) | 1979-10-25 |
| GB2019415B (en) | 1982-10-20 |
| NO791332L (no) | 1979-10-25 |
| NO154523C (no) | 1986-10-08 |
| DK167679A (da) | 1980-10-25 |
| DE2916537A1 (de) | 1979-10-31 |
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