DE947632C - Verfahren zum Verbinden von nichtporoesen Werkstoffen, insbesondere Metallen - Google Patents
Verfahren zum Verbinden von nichtporoesen Werkstoffen, insbesondere MetallenInfo
- Publication number
- DE947632C DE947632C DEP27918D DEP0027918D DE947632C DE 947632 C DE947632 C DE 947632C DE P27918 D DEP27918 D DE P27918D DE P0027918 D DEP0027918 D DE P0027918D DE 947632 C DE947632 C DE 947632C
- Authority
- DE
- Germany
- Prior art keywords
- parts
- aluminum
- ethylene oxide
- adhesive
- resin
- 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
- 238000000034 method Methods 0.000 title claims description 27
- 229910052751 metal Inorganic materials 0.000 title claims description 22
- 239000002184 metal Substances 0.000 title claims description 22
- 150000002739 metals Chemical class 0.000 title claims description 17
- 239000011148 porous material Substances 0.000 title claims 2
- 239000000463 material Substances 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 31
- 238000001723 curing Methods 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- 239000004848 polyfunctional curative Substances 0.000 claims description 16
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 15
- 150000002989 phenols Chemical class 0.000 claims description 13
- 229920003002 synthetic resin Polymers 0.000 claims description 11
- 239000000057 synthetic resin Substances 0.000 claims description 11
- 238000004026 adhesive bonding Methods 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 150000008064 anhydrides Chemical class 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
- 150000001735 carboxylic acids Chemical class 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 238000013007 heat curing Methods 0.000 claims description 2
- 150000007529 inorganic bases Chemical class 0.000 claims description 2
- 150000007530 organic bases Chemical class 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 238000003825 pressing Methods 0.000 claims 1
- 229920001187 thermosetting polymer Polymers 0.000 claims 1
- 239000000853 adhesive Substances 0.000 description 61
- 230000001070 adhesive effect Effects 0.000 description 61
- 229920005989 resin Polymers 0.000 description 55
- 239000011347 resin Substances 0.000 description 55
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 53
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 50
- 229910052782 aluminium Inorganic materials 0.000 description 49
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 16
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 16
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 15
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- 229920000877 Melamine resin Polymers 0.000 description 9
- 229910052802 copper Inorganic materials 0.000 description 9
- 239000010949 copper Substances 0.000 description 9
- 229910052742 iron Inorganic materials 0.000 description 9
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 9
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 8
- 229910052725 zinc Inorganic materials 0.000 description 8
- 239000011701 zinc Substances 0.000 description 8
- 239000011521 glass Substances 0.000 description 7
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 7
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 7
- 235000011121 sodium hydroxide Nutrition 0.000 description 7
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 6
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
- VRAIHTAYLFXSJJ-UHFFFAOYSA-N alumane Chemical compound [AlH3].[AlH3] VRAIHTAYLFXSJJ-UHFFFAOYSA-N 0.000 description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229920001169 thermoplastic Polymers 0.000 description 6
- 239000004416 thermosoftening plastic Substances 0.000 description 6
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- -1 ethylene oxide groups Ethylene oxide derivatives Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- CRUILBNAQILVHZ-UHFFFAOYSA-N 1,2,3-trimethoxybenzene Chemical compound COC1=CC=CC(OC)=C1OC CRUILBNAQILVHZ-UHFFFAOYSA-N 0.000 description 4
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 4
- IYDYVVVAQKFGBS-UHFFFAOYSA-N 2,4,6-triphenoxy-1,3,5-triazine Chemical compound N=1C(OC=2C=CC=CC=2)=NC(OC=2C=CC=CC=2)=NC=1OC1=CC=CC=C1 IYDYVVVAQKFGBS-UHFFFAOYSA-N 0.000 description 4
- 229910001369 Brass Inorganic materials 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- 239000010951 brass Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229910052573 porcelain Inorganic materials 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 241000784732 Lycaena phlaeas Species 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 235000010333 potassium nitrate Nutrition 0.000 description 3
- 239000004323 potassium nitrate Substances 0.000 description 3
- IUCNNRFELLGMOO-UHFFFAOYSA-N 1,2,3-tris(phenylmethoxy)benzene Chemical compound C=1C=CC=CC=1COC(C=1OCC=2C=CC=CC=2)=CC=CC=1OCC1=CC=CC=C1 IUCNNRFELLGMOO-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
- CHOSFPFCXKKOHO-UHFFFAOYSA-N 2-n,4-n-dimethyl-1,3,5-triazine-2,4,6-triamine Chemical compound CNC1=NC(N)=NC(NC)=N1 CHOSFPFCXKKOHO-UHFFFAOYSA-N 0.000 description 2
- YZEZMSPGIPTEBA-UHFFFAOYSA-N 2-n-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(NC=2N=C(N)N=C(N)N=2)=N1 YZEZMSPGIPTEBA-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 229910001335 Galvanized steel Inorganic materials 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- SLABEOONBHLKSD-UHFFFAOYSA-N O=S1(=O)C(C=C2)=CC=C2OOC2=CC=C1C=C2 Chemical class O=S1(=O)C(C=C2)=CC=C2OOC2=CC=C1C=C2 SLABEOONBHLKSD-UHFFFAOYSA-N 0.000 description 2
- 229920002396 Polyurea Polymers 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000008397 galvanized steel Substances 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- UDGSVBYJWHOHNN-UHFFFAOYSA-N n',n'-diethylethane-1,2-diamine Chemical compound CCN(CC)CCN UDGSVBYJWHOHNN-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 2
- 150000007519 polyprotic acids Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
- JBQMAAJJRTWUPQ-UHFFFAOYSA-N 1,2-diphenylguanidine Chemical compound C1(=CC=CC=C1)NC(NC1=CC=CC=C1)=N.C1(=CC=CC=C1)NC(=N)NC1=CC=CC=C1 JBQMAAJJRTWUPQ-UHFFFAOYSA-N 0.000 description 1
- 150000000182 1,3,5-triazines Chemical class 0.000 description 1
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- DFUGJTBMQKRCPI-UHFFFAOYSA-N 2,4,6-trimethoxy-1,3,5-triazine Chemical compound COC1=NC(OC)=NC(OC)=N1 DFUGJTBMQKRCPI-UHFFFAOYSA-N 0.000 description 1
- LSYJAEPSXPMRGV-UHFFFAOYSA-N 6-phenoxy-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(OC=2C=CC=CC=2)=N1 LSYJAEPSXPMRGV-UHFFFAOYSA-N 0.000 description 1
- 244000059549 Borneo rubber Species 0.000 description 1
- QEQCJYGLEZQLDC-UHFFFAOYSA-N C1=CC=C2C(=O)OC(=O)C2=C1.C1=CC=C2C(=O)OC(=O)C2=C1.C1=CC=C2C(=O)OC(=O)C2=C1 Chemical compound C1=CC=C2C(=O)OC(=O)C2=C1.C1=CC=C2C(=O)OC(=O)C2=C1.C1=CC=C2C(=O)OC(=O)C2=C1 QEQCJYGLEZQLDC-UHFFFAOYSA-N 0.000 description 1
- 241000428199 Mustelinae Species 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 240000003085 Quassia amara Species 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- KNXVOGGZOFOROK-UHFFFAOYSA-N trimagnesium;dioxido(oxo)silane;hydroxy-oxido-oxosilane Chemical compound [Mg+2].[Mg+2].[Mg+2].O[Si]([O-])=O.O[Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O KNXVOGGZOFOROK-UHFFFAOYSA-N 0.000 description 1
- NNPPMTNAJDCUHE-UHFFFAOYSA-N trimethylmethane Natural products CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002023 wood Substances 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
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4021—Ureas; Thioureas; Guanidines; Dicyandiamides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5046—Amines heterocyclic
- C08G59/5053—Amines heterocyclic containing only nitrogen as a heteroatom
- C08G59/508—Amines heterocyclic containing only nitrogen as a heteroatom having three nitrogen atoms in the ring
- C08G59/5086—Triazines; Melamines; Guanamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/56—Amines together with other curing agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31515—As intermediate layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31515—As intermediate layer
- Y10T428/31518—Next to glass or quartz
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31515—As intermediate layer
- Y10T428/31522—Next to metal
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH2082946 | 1945-07-13 | ||
| CH2083046 | 1946-05-28 | ||
| CH264818T | 1946-10-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE947632C true DE947632C (de) | 1956-08-23 |
Family
ID=32302815
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEP27918D Expired DE947632C (de) | 1945-07-13 | 1948-12-30 | Verfahren zum Verbinden von nichtporoesen Werkstoffen, insbesondere Metallen |
| DEP27917A Expired DE958860C (de) | 1945-07-13 | 1948-12-30 | Verfahren und Klebmittel zum Verkleben von nichtporoesen Werkstoffen, insbesondere Metallen |
| DEP27916A Expired DE964978C (de) | 1945-07-13 | 1948-12-30 | Verfahren und Klebmittel zum Verkleben von nichtporoesen Werkstoffen |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEP27917A Expired DE958860C (de) | 1945-07-13 | 1948-12-30 | Verfahren und Klebmittel zum Verkleben von nichtporoesen Werkstoffen, insbesondere Metallen |
| DEP27916A Expired DE964978C (de) | 1945-07-13 | 1948-12-30 | Verfahren und Klebmittel zum Verkleben von nichtporoesen Werkstoffen |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US2682490A (en:Method) |
| BE (3) | BE466573A (en:Method) |
| CH (4) | CH251647A (en:Method) |
| DE (3) | DE947632C (en:Method) |
| FR (4) | FR930609A (en:Method) |
| GB (3) | GB629111A (en:Method) |
| LU (3) | LU28060A1 (en:Method) |
| NL (3) | NL72483C (en:Method) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE972786C (de) * | 1953-08-28 | 1959-10-08 | Ciba Geigy | Verfahren zur Erhoehung der Gebrauchsdauer von hitzehaertbaren Polyepoxydverbindungen |
| DE1086236B (de) * | 1955-10-07 | 1960-08-04 | Du Pont | Verfahren zur Herstellung von als Aushaertemittel fuer Epoxyharze geeigneten N, N'-Bis-[(1-aminocycloalkyl)-methyl]-piperazinen |
| DE1100278B (de) * | 1956-10-05 | 1961-02-23 | Devoe & Raynolds Co | Verfahren zum Haerten von harzartigen Epoxydverbindungen |
| DE1109367B (de) * | 1957-08-12 | 1961-06-22 | Devoe & Raynolds Co | Verfahren zum Haerten von harzartigen Polyepoxyden |
| DE1177982B (de) * | 1957-08-24 | 1964-09-10 | Herberts & Co Gmbh Dr Kurt | Verfahren zur Herstellung von bemusterten Kunststoffoberflaechen unter Verwendung von Epoxyharzen |
Families Citing this family (94)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE489971A (en:Method) * | 1948-07-05 | |||
| BE496766A (en:Method) * | 1949-07-05 | |||
| US3142657A (en) * | 1949-08-12 | 1964-07-28 | Ciba Ltd | Elastic reaction product of a polyepoxide, a glycol, and an acid anhydride |
| BE498918A (en:Method) * | 1949-10-25 | 1900-01-01 | ||
| CH286859A (de) * | 1950-01-16 | 1952-11-15 | Beck & Co Gmbh Dr | Verfahren zur Herstellung von Kunstharzlacken. |
| BE503546A (en:Method) * | 1950-05-27 | |||
| US2659710A (en) * | 1951-07-26 | 1953-11-17 | Gen Electric | Phenol alcohol-epichlorohydrin reaction products |
| NL171616B (nl) * | 1951-08-07 | Occident Ets | Afdichtingsinrichting. | |
| NL173809B (nl) * | 1951-11-17 | Rca Corp | Beeldopneeminrichting met kleurcodeerstrookfilterstelsel. | |
| BE516436A (en:Method) * | 1951-12-21 | |||
| US2716099A (en) * | 1952-01-19 | 1955-08-23 | Shell Dev | Epoxy resins from alkyl phenol novolac resins |
| US2865886A (en) * | 1952-02-11 | 1958-12-23 | Devoe & Raynolds Co | Polyethylene polyamine-epoxide compositions |
| US2865888A (en) * | 1952-02-11 | 1958-12-23 | Devoe & Raynolds Co | Amine-epoxide compositions |
| DE1076366B (de) * | 1952-03-15 | 1960-02-25 | Henkel & Cie Gmbh | Verwendung von schwefel- und stickstoffhaltigen Verbindungen als Haertungsmittel fuer harzartige Verbindungen mit mehreren Epoxydgruppen im Molekuel |
| US2714098A (en) * | 1952-05-15 | 1955-07-26 | Gen Electric | Phenolic resinous compositions |
| US2783214A (en) * | 1952-06-02 | 1957-02-26 | Cordo Chemical Corp | Method of producing a solidified cured resin |
| US2744845A (en) * | 1952-08-22 | 1956-05-08 | Gen Electric | Chlorinated maleic adduct-ethoxyline resinous compositions |
| US2773048A (en) * | 1952-08-25 | 1956-12-04 | Honeywell Regulator Co | Epoxy resin composition containing para, para' diamino diphenylmethane |
| DE968500C (de) * | 1952-09-26 | 1958-02-27 | Henkel & Cie Gmbh | Klebmittel zur Verklebung von Werkstoffen |
| DE980061C (de) * | 1952-10-02 | 1970-01-02 | Shell Oil Co | Verfahren zur Herstellung von Formkoerpern auf der Basis von Polyaddukten |
| US2707177A (en) * | 1952-11-29 | 1955-04-26 | Gen Electric | Ethoxyline-triallyl cyanurate resinous compositions |
| BE527446A (en:Method) * | 1953-03-30 | |||
| NL95049C (en:Method) * | 1953-07-21 | |||
| US2939859A (en) * | 1954-03-31 | 1960-06-07 | Shell Oil Co | Process for preparing resinified product from polyepoxy polyether and aromatic-substituted-alkene-1 and composition for production of said product |
| DE975979C (de) * | 1954-08-11 | 1963-01-03 | Concordia Maschinen Und Elek Z | Auf Zug und Druck beanspruchter stabfoermiger Antriebsisolator fuer elektrische Schalter |
| FR1141899A (fr) * | 1954-08-16 | 1957-09-11 | Minnesota Mining & Mfg | Durcissement des résines épichlorhydrine-phénol |
| DE973052C (de) * | 1954-10-27 | 1959-11-26 | Siemens Ag | Elektrische Raumabschirmung aus Metallfolien |
| US2967838A (en) * | 1954-11-15 | 1961-01-10 | Dow Chemical Co | New synthetic drying oils |
| US2893973A (en) * | 1954-12-10 | 1959-07-07 | Gen Aniline & Film Corp | Liquefied m-phenylenediamine compositions for curing epoxy ether resins |
| US2892006A (en) * | 1954-12-30 | 1959-06-23 | Sonotone Corp | Terminal seals for alkaline electric batteries |
| US2828236A (en) * | 1954-12-30 | 1958-03-25 | Minnesota Mining & Mfg | Application of perfluorochloroolefin polymer coatings to base materials |
| US2847395A (en) * | 1955-06-13 | 1958-08-12 | Minnesota Mining & Mfg | Stable heat-curing epoxy resin compositions |
| DE1056686B (de) * | 1955-07-09 | 1959-05-06 | Calor Emag Elektrizitaets Ag | Hochspannungs-Durchfuehrungsisolator |
| US3214408A (en) * | 1955-08-18 | 1965-10-26 | Gen Electric | Ethoxyline resin compositions |
| NL210738A (en:Method) * | 1955-09-21 | |||
| NL105578C (en:Method) * | 1955-11-17 | |||
| US2864805A (en) * | 1955-12-05 | 1958-12-16 | Devoe & Raynolds Co | Epoxide resins |
| US2853467A (en) * | 1956-01-04 | 1958-09-23 | Gen Aniline & Film Corp | Liquid aromatic diamines as curing agents for epoxy ether resins |
| DE1019083B (de) * | 1956-01-28 | 1957-11-07 | Bayer Ag | Verfahren zur Herstellung von Kunststoffen durch Haerten von Epoxyverbindungen |
| DE1044202B (de) * | 1956-03-07 | 1958-11-20 | Deutsche Bundespost | Verfahren zur Herstellung von Masten fuer den Freileitungsbau, insbesondere fuer Fernmeldeleitungen, einschliesslich Traversen, Isolatorstuetzen und Isolierkoerpern |
| DE1079833B (de) * | 1956-03-12 | 1960-04-14 | Minnesota Mining & Mfg | Verwendung von latenten Haertungsmitteln fuer Epoxyharze |
| US2967161A (en) * | 1956-03-27 | 1961-01-03 | Pittsburgh Plate Glass Co | Interpolymer of allylepoxy resin and polyamide resin |
| US2947712A (en) * | 1956-06-11 | 1960-08-02 | Devoe & Raynolds Co | Epoxide resin compositions |
| US2908664A (en) * | 1956-06-11 | 1959-10-13 | Devoe & Raynolds Co | Modified epoxide resins |
| US2934521A (en) * | 1956-06-11 | 1960-04-26 | Devoe & Raynolds Co | Epoxide resin compositions |
| US2945638A (en) * | 1956-07-10 | 1960-07-19 | Westinghouse Electric Corp | Composite laminated tube |
| US2897179A (en) * | 1956-07-18 | 1959-07-28 | Union Carbide Corp | Hardener for epoxy resin composition |
| US2986546A (en) * | 1956-11-15 | 1961-05-30 | Shell Oil Co | Adhesive compositions and their preparation |
| US3028251A (en) * | 1956-11-20 | 1962-04-03 | Polymer Corp | Method of coating an article with a powdered resin composition and method of making the composition |
| US2881090A (en) * | 1957-03-13 | 1959-04-07 | Union Carbide Corp | Impregnation of carbonaceous materials |
| US3029730A (en) * | 1957-04-10 | 1962-04-17 | Meredith Publishing Company | Method of forming laminated printing plate with plastic core |
| US3100080A (en) * | 1957-05-27 | 1963-08-06 | American Railroad Curvelining | Railway rail joint |
| DE1158164B (de) * | 1957-06-08 | 1963-11-28 | Fleischmann Geb | Scheibenkommutator fuer elektrische Spielzeugmotoren u. dgl. |
| US2951779A (en) * | 1957-08-06 | 1960-09-06 | Borden Co | Plywood containers |
| US2899399A (en) * | 1957-08-27 | 1959-08-11 | Ethoxyline resin-shellac-dicyandiamide insulation composition | |
| US3016362A (en) * | 1957-09-05 | 1962-01-09 | Pittsburgh Plate Glass Co | Blend of a halogenated aromatic polyglycidyl ether and an aliphatic polyglycidyl ether |
| BE571981A (en:Method) * | 1957-10-21 | 1900-01-01 | ||
| US3063965A (en) * | 1957-11-25 | 1962-11-13 | Union Carbide Corp | Polyepoxide compositions |
| US3338863A (en) * | 1957-12-26 | 1967-08-29 | Polymer Corp | Powdered coating compositions and the method for their application |
| NL235079A (en:Method) * | 1958-01-13 | 1900-01-01 | ||
| US3102043A (en) * | 1958-01-30 | 1963-08-27 | Fluidized bed coating method | |
| US2965220A (en) * | 1958-02-13 | 1960-12-20 | Westinghouse Electric Corp | Spinning bucket |
| NL239419A (en:Method) * | 1958-05-23 | |||
| US3032460A (en) * | 1958-07-23 | 1962-05-01 | Gen Tire & Rubber Co | Adhesion of polyvinyl chloride |
| US3106769A (en) * | 1958-08-01 | 1963-10-15 | Westinghouse Electric Corp | Magnetic cores hermetically sealed within metal core boxes |
| US3031434A (en) * | 1958-08-11 | 1962-04-24 | Glidden Co | Method of curing epoxy components and heat-curable epoxy compositions |
| US3245329A (en) * | 1958-10-30 | 1966-04-12 | Reliance Steel Prod Co | Method of surfacing paved areas |
| US3071560A (en) * | 1959-02-17 | 1963-01-01 | Nopco Chem Co | Stable vinyl resin containing a reaction product of epichlorhydrin and a sulfone |
| US3095550A (en) * | 1959-04-09 | 1963-06-25 | Timothy J Kilduff | Polytetrafluoroethylene waveguide window construction |
| US3063760A (en) * | 1959-06-22 | 1962-11-13 | Plastic Applicators | Drill stem protector |
| US3047537A (en) * | 1959-06-25 | 1962-07-31 | Dow Chemical Co | Epoxy resin composition |
| US3087060A (en) * | 1959-06-30 | 1963-04-23 | Robert J Omohundro | Scintillation counter |
| NL254742A (en:Method) * | 1959-08-11 | 1900-01-01 | ||
| US3159595A (en) * | 1960-08-11 | 1964-12-01 | Shell Oil Co | Blending crystalline 2, 2-bis(2, 3-epoxypropoxyphenyl) propane with curing agent |
| DE1262394B (de) * | 1960-10-03 | 1968-03-07 | Sanders Associates Inc | Verfahren zum Herstellen von gedruckten Schaltungen |
| US3277049A (en) * | 1961-03-13 | 1966-10-04 | Air Prod & Chem | Curing epoxy resins with diaza-aromatic tertiary amines |
| NL282084A (en:Method) * | 1961-08-15 | |||
| US3306872A (en) * | 1961-10-16 | 1967-02-28 | Shell Oil Co | Method for producing a polyether resin |
| US3277052A (en) * | 1962-02-06 | 1966-10-04 | Shell Oil Co | Process for curing polyepoxides and resulting products |
| BE632644A (en:Method) * | 1962-02-23 | 1900-01-01 | ||
| BE629380A (en:Method) * | 1962-03-09 | |||
| US3188362A (en) * | 1962-07-06 | 1965-06-08 | Furane Plastics | Semi-rigid epoxy resin compositions and method |
| GB1054555A (en:Method) * | 1962-09-25 | |||
| US3225004A (en) * | 1962-10-11 | 1965-12-21 | Dwight E Peerman | Thermosetting plastic compositions derived from polyglycidyl ethers of bis (p-hydroxyphenyl) sulfones and certain fatty guanamines and process of preparing same |
| US3271509A (en) * | 1963-04-12 | 1966-09-06 | Westinghouse Electric Corp | Electrical insulation for condenser bushings and the like |
| US3214409A (en) * | 1963-04-29 | 1965-10-26 | Gen Mills Inc | Epoxidized novolac-fatty guanamine composition |
| US3285745A (en) * | 1963-07-01 | 1966-11-15 | Union Carbide Corp | Laminated planographic printing plates |
| US3420794A (en) * | 1963-08-29 | 1969-01-07 | Shell Oil Co | Process for curing polyepoxides with a polyamine and resulting products |
| US4120913A (en) * | 1976-12-10 | 1978-10-17 | Westinghouse Electric Corp. | Epoxy-amine adhesive compositions |
| US4113684A (en) * | 1976-12-10 | 1978-09-12 | Westinghouse Electric Corp. | Low temperature cure epoxy-amine adhesive compositions |
| DE2743015C2 (de) * | 1977-09-23 | 1982-07-15 | Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München | Verfahren zum Härten von Epoxydharzen |
| CA1121930A (en) * | 1977-12-29 | 1982-04-13 | Alkis Christofas | Synergistic primer for fluoropolymer coatings |
| GB1604865A (en) * | 1977-12-29 | 1981-12-16 | Secr Defence | Projectile tail fin units |
| US4500703A (en) * | 1983-04-04 | 1985-02-19 | W. R. Grace & Co. | Reactive adhesive dispersion and method of use |
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|---|---|---|---|---|
| US2136928A (en) * | 1934-12-10 | 1938-11-15 | Ig Farbenindustrie Ag | Manufacture of amines of high molecular weight, which are rich in nitrogen |
| DE676117C (de) * | 1934-12-11 | 1939-05-26 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung hochmolekularer Polyamine |
| FR859061A (fr) * | 1938-08-23 | 1940-12-10 | Trey Ag Geb De | Procédé de préparation de résines synthétiques |
| FR907172A (fr) * | 1943-06-16 | 1946-03-05 | Trey Freres De | Procédé de fabrication de résines synthétiques durcissables |
| DE882761C (de) * | 1939-07-11 | 1953-07-13 | Henkel & Cie Gmbh | Verfahren zum Herstellen von Holzschichtkoerpern |
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| US1019407A (en) * | 1910-12-16 | 1912-03-05 | Gen Bakelite Company | Method of uniting objects. |
| US2318184A (en) * | 1936-01-18 | 1943-05-04 | Walter H Liebman | Laminated sheet and method of producing same |
| DE700843C (de) * | 1938-07-10 | 1941-01-02 | Emil Lumbeck | Verfahren und Klebemittel zur Herstellung von Buechern |
| US2414414A (en) * | 1942-10-06 | 1947-01-14 | Pennsylvania Coal Products Com | Method of bonding materials with a cold-setting dihydroxy benzene aldehyde adhesive |
| US2479342A (en) * | 1943-12-09 | 1949-08-16 | United Aircraft Corp | Composite structure for use in aircraft construction |
| US2585115A (en) * | 1945-09-18 | 1952-02-12 | Devoe & Raynolds Co | Amine-epoxide compositions |
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| NL68092C (en:Method) * | 1947-06-11 |
-
0
- LU LU28607D patent/LU28607A1/xx unknown
- NL NL67492D patent/NL67492C/xx active
- NL NL73161D patent/NL73161C/xx active
- BE BE474687D patent/BE474687A/xx unknown
- BE BE476967D patent/BE476967A/xx unknown
- LU LU28519D patent/LU28519A1/xx unknown
- NL NL72483D patent/NL72483C/xx active
- BE BE466573D patent/BE466573A/xx unknown
- LU LU28060D patent/LU28060A1/xx unknown
-
1945
- 1945-07-13 CH CH251647D patent/CH251647A/de unknown
-
1946
- 1946-07-12 GB GB2082946A patent/GB629111A/en not_active Expired
- 1946-07-13 FR FR930609D patent/FR930609A/fr not_active Expired
- 1946-07-19 CH CH262480D patent/CH262480A/de unknown
- 1946-07-19 CH CH262479D patent/CH262479A/de unknown
- 1946-10-25 CH CH264818D patent/CH264818A/de unknown
-
1947
- 1947-07-10 FR FR57612D patent/FR57612E/fr not_active Expired
- 1947-07-14 GB GB1863647A patent/GB630647A/en not_active Expired
- 1947-07-17 FR FR57655D patent/FR57655E/fr not_active Expired
- 1947-10-17 FR FR57737D patent/FR57737E/fr not_active Expired
- 1947-10-20 US US78101047 patent/US2682490A/en not_active Expired - Lifetime
- 1947-10-22 GB GB2824447A patent/GB630663A/en not_active Expired
-
1948
- 1948-12-30 DE DEP27918D patent/DE947632C/de not_active Expired
- 1948-12-30 DE DEP27917A patent/DE958860C/de not_active Expired
- 1948-12-30 DE DEP27916A patent/DE964978C/de not_active Expired
-
1952
- 1952-05-27 US US29031252 patent/US2786794A/en not_active Expired - Lifetime
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| US2136928A (en) * | 1934-12-10 | 1938-11-15 | Ig Farbenindustrie Ag | Manufacture of amines of high molecular weight, which are rich in nitrogen |
| DE676117C (de) * | 1934-12-11 | 1939-05-26 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung hochmolekularer Polyamine |
| FR859061A (fr) * | 1938-08-23 | 1940-12-10 | Trey Ag Geb De | Procédé de préparation de résines synthétiques |
| DE749512C (de) * | 1938-08-23 | 1944-11-24 | Verfahren zur Herstellung von haertbaren Kunstharzen | |
| DE882761C (de) * | 1939-07-11 | 1953-07-13 | Henkel & Cie Gmbh | Verfahren zum Herstellen von Holzschichtkoerpern |
| FR907172A (fr) * | 1943-06-16 | 1946-03-05 | Trey Freres De | Procédé de fabrication de résines synthétiques durcissables |
| US2444333A (en) * | 1943-06-16 | 1948-06-29 | Trey Freres S A De | Process for the manufacture of thermosetting synthetic resins by the polymerization of alkylene oxide derivatives |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE972786C (de) * | 1953-08-28 | 1959-10-08 | Ciba Geigy | Verfahren zur Erhoehung der Gebrauchsdauer von hitzehaertbaren Polyepoxydverbindungen |
| DE1086236B (de) * | 1955-10-07 | 1960-08-04 | Du Pont | Verfahren zur Herstellung von als Aushaertemittel fuer Epoxyharze geeigneten N, N'-Bis-[(1-aminocycloalkyl)-methyl]-piperazinen |
| DE1100278B (de) * | 1956-10-05 | 1961-02-23 | Devoe & Raynolds Co | Verfahren zum Haerten von harzartigen Epoxydverbindungen |
| DE1109367B (de) * | 1957-08-12 | 1961-06-22 | Devoe & Raynolds Co | Verfahren zum Haerten von harzartigen Polyepoxyden |
| DE1177982B (de) * | 1957-08-24 | 1964-09-10 | Herberts & Co Gmbh Dr Kurt | Verfahren zur Herstellung von bemusterten Kunststoffoberflaechen unter Verwendung von Epoxyharzen |
Also Published As
| Publication number | Publication date |
|---|---|
| FR57737E (fr) | 1953-05-04 |
| FR930609A (fr) | 1948-01-30 |
| NL72483C (en:Method) | 1900-01-01 |
| CH262479A (de) | 1949-06-30 |
| BE466573A (en:Method) | 1900-01-01 |
| DE964978C (de) | 1957-05-29 |
| GB630663A (en) | 1949-10-18 |
| GB629111A (en) | 1949-09-13 |
| US2786794A (en) | 1957-03-26 |
| FR57655E (fr) | 1953-05-04 |
| LU28519A1 (en:Method) | |
| NL67492C (en:Method) | 1900-01-01 |
| CH251647A (de) | 1947-11-15 |
| GB630647A (en) | 1949-10-18 |
| US2682490A (en) | 1954-06-29 |
| CH262480A (de) | 1949-06-30 |
| DE958860C (de) | 1957-02-28 |
| CH264818A (de) | 1949-10-31 |
| BE474687A (en:Method) | 1900-01-01 |
| LU28060A1 (en:Method) | |
| LU28607A1 (en:Method) | |
| NL73161C (en:Method) | 1900-01-01 |
| BE476967A (en:Method) | 1900-01-01 |
| FR57612E (fr) | 1953-03-17 |
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