DE2125247C3 - Verfahren zum Applizieren von Lacken, Vergußmassen, Spachtelmassen, Überzugs- und Beschichtungsmassen - Google Patents
Verfahren zum Applizieren von Lacken, Vergußmassen, Spachtelmassen, Überzugs- und BeschichtungsmassenInfo
- Publication number
- DE2125247C3 DE2125247C3 DE2125247A DE2125247A DE2125247C3 DE 2125247 C3 DE2125247 C3 DE 2125247C3 DE 2125247 A DE2125247 A DE 2125247A DE 2125247 A DE2125247 A DE 2125247A DE 2125247 C3 DE2125247 C3 DE 2125247C3
- Authority
- DE
- Germany
- Prior art keywords
- compounds
- weight
- divalent
- water
- parts
- 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
- 150000001875 compounds Chemical class 0.000 title claims description 10
- 238000005266 casting Methods 0.000 title claims description 8
- 238000000034 method Methods 0.000 title claims description 8
- 238000000576 coating method Methods 0.000 title claims description 7
- 239000003973 paint Substances 0.000 title claims description 5
- 239000011248 coating agent Substances 0.000 title description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 19
- 239000005056 polyisocyanate Substances 0.000 claims description 19
- 229920001228 polyisocyanate Polymers 0.000 claims description 19
- -1 enamine compounds Chemical class 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 239000008199 coating composition Substances 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- 150000001728 carbonyl compounds Chemical class 0.000 claims description 3
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 7
- 150000004985 diamines Chemical group 0.000 description 7
- 150000002081 enamines Chemical class 0.000 description 7
- POSWICCRDBKBMH-UHFFFAOYSA-N 3,3,5-trimethylcyclohexan-1-one Chemical compound CC1CC(=O)CC(C)(C)C1 POSWICCRDBKBMH-UHFFFAOYSA-N 0.000 description 6
- 150000001299 aldehydes Chemical class 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000005058 Isophorone diisocyanate Substances 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 5
- 150000002576 ketones Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 3
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- AMUBKBXGFDIMDJ-UHFFFAOYSA-N 3-heptyl-1,2-bis(9-isocyanatononyl)-4-pentylcyclohexane Chemical compound CCCCCCCC1C(CCCCC)CCC(CCCCCCCCCN=C=O)C1CCCCCCCCCN=C=O AMUBKBXGFDIMDJ-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000003997 cyclic ketones Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- PYOLJOJPIPCRDP-UHFFFAOYSA-N 1,1,3-trimethylcyclohexane Chemical compound CC1CCCC(C)(C)C1 PYOLJOJPIPCRDP-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- SWRRWODUBVHJBC-UHFFFAOYSA-N 1-(2-piperidin-1-ylpropan-2-yl)piperidine Chemical compound N1(CCCCC1)C(C)(C)N1CCCCC1 SWRRWODUBVHJBC-UHFFFAOYSA-N 0.000 description 1
- AVFZQHWFGFKQIG-UHFFFAOYSA-N 2,2,3-trimethylcyclopentan-1-one Chemical compound CC1CCC(=O)C1(C)C AVFZQHWFGFKQIG-UHFFFAOYSA-N 0.000 description 1
- ZUYKJZQOPXDNOK-UHFFFAOYSA-N 2-(ethylamino)-2-thiophen-2-ylcyclohexan-1-one;hydrochloride Chemical class Cl.C=1C=CSC=1C1(NCC)CCCCC1=O ZUYKJZQOPXDNOK-UHFFFAOYSA-N 0.000 description 1
- UNNGUFMVYQJGTD-UHFFFAOYSA-N 2-Ethylbutanal Chemical compound CCC(CC)C=O UNNGUFMVYQJGTD-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- MGYGFNQQGAQEON-UHFFFAOYSA-N 4-tolyl isocyanate Chemical compound CC1=CC=C(N=C=O)C=C1 MGYGFNQQGAQEON-UHFFFAOYSA-N 0.000 description 1
- CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical group [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000004705 aldimines Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- XXKOQQBKBHUATC-UHFFFAOYSA-N cyclohexylmethylcyclohexane Chemical compound C1CCCCC1CC1CCCCC1 XXKOQQBKBHUATC-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000021190 leftovers Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
Classifications
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/68—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
- C07C209/78—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton from carbonyl compounds, e.g. from formaldehyde, and amines having amino groups bound to carbon atoms of six-membered aromatic rings, with formation of methylene-diarylamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/02—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C211/09—Diamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/33—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C211/34—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of a saturated carbon skeleton
- C07C211/36—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of a saturated carbon skeleton containing at least two amino groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
- C07D211/14—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
- C07D295/033—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3253—Polyamines being in latent form
- C08G18/3256—Reaction products of polyamines with aldehydes or ketones
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3293—Hydroxyamines containing heterocyclic groups
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3296—Hydroxyamines being in latent form
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2116882A DE2116882C3 (de) | 1971-04-06 | 1971-04-06 | Enaminverbindungen und deren Herstellung |
| DE2125247A DE2125247C3 (de) | 1971-04-06 | 1971-04-06 | Verfahren zum Applizieren von Lacken, Vergußmassen, Spachtelmassen, Überzugs- und Beschichtungsmassen |
| DE19712167133 DE2167133C3 (de) | 1971-04-06 | 1971-04-06 | Di-Enamin-Verbindungen |
| US240762A US3865791A (en) | 1971-04-06 | 1972-04-03 | Certain enamine compounds and methods for making and using the same |
| AT200274*1A AT324513B (de) | 1971-04-06 | 1972-04-05 | Lagerstabile mischung |
| SE7204389A SE405256B (sv) | 1971-04-06 | 1972-04-05 | Sett att framstella tetningsmassor genom omsettning av blandningar av isocyanatkomponenter, bi- eller polyfunktionella enaminer och vatten |
| AT291372A AT329016B (de) | 1971-04-06 | 1972-04-05 | Verfahren zur herstellung neuer di-enamine |
| FR7211899A FR2136178A5 (enExample) | 1971-04-06 | 1972-04-05 | |
| NLAANVRAGE7204634,A NL171816C (nl) | 1971-04-06 | 1972-04-06 | Werkwijze massa's, plamuurmassa's, dek- en bekledingsmassa's alsmede gevormde voortbrengselen. |
| BE781756A BE781756A (fr) | 1971-04-06 | 1972-04-06 | Enamines, leur preparation et leur utilisation |
| GB1589972A GB1394732A (en) | 1971-04-06 | 1972-04-06 | Enamine compounds their manufacture and use |
| AT724174A AT338276B (de) | 1971-04-06 | 1974-09-09 | Verfahren zur herstellung von neuen, mindestens eine enamin- und mindestens eine ketimin- und/oder aldimingruppe enthaltenden verbindungen |
| US05/520,356 US3941753A (en) | 1971-04-06 | 1974-11-01 | Prepolymers of polyisocyanates with hydroxy-enamines or hydroxy-ketimines |
| AT296978A AT377275B (de) | 1971-04-06 | 1978-04-25 | Lagerstabile mischung |
| NLAANVRAGE8203663,A NL177219C (nl) | 1971-04-06 | 1982-09-21 | Werkwijze voor het bereiden van prepolymeren en van stabiele mengsels; gevormde voortbrengselen. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2116882A DE2116882C3 (de) | 1971-04-06 | 1971-04-06 | Enaminverbindungen und deren Herstellung |
| DE2125247A DE2125247C3 (de) | 1971-04-06 | 1971-04-06 | Verfahren zum Applizieren von Lacken, Vergußmassen, Spachtelmassen, Überzugs- und Beschichtungsmassen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2125247A1 DE2125247A1 (de) | 1972-10-19 |
| DE2125247B2 DE2125247B2 (de) | 1977-08-11 |
| DE2125247C3 true DE2125247C3 (de) | 1981-07-23 |
Family
ID=25760937
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2125247A Expired DE2125247C3 (de) | 1971-04-06 | 1971-04-06 | Verfahren zum Applizieren von Lacken, Vergußmassen, Spachtelmassen, Überzugs- und Beschichtungsmassen |
| DE2116882A Expired DE2116882C3 (de) | 1971-04-06 | 1971-04-06 | Enaminverbindungen und deren Herstellung |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2116882A Expired DE2116882C3 (de) | 1971-04-06 | 1971-04-06 | Enaminverbindungen und deren Herstellung |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3865791A (enExample) |
| AT (2) | AT324513B (enExample) |
| BE (1) | BE781756A (enExample) |
| DE (2) | DE2125247C3 (enExample) |
| FR (1) | FR2136178A5 (enExample) |
| GB (1) | GB1394732A (enExample) |
| NL (1) | NL171816C (enExample) |
| SE (1) | SE405256B (enExample) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2718393C2 (de) * | 1977-04-26 | 1985-05-09 | Schering AG, 1000 Berlin und 4709 Bergkamen | Verfahren zur Herstellung von für Prepolymere geeigneten hydroxylgruppenhaltigen Monoenaminen |
| DE2356213C2 (de) * | 1973-11-10 | 1986-11-13 | Schering AG, 1000 Berlin und 4709 Bergkamen | Durch Ketimingruppen terminierte Prepolymere und Verfahren zu ihrer Herstellung |
| DE2651479C2 (de) * | 1976-11-11 | 1986-03-20 | Schering AG, 1000 Berlin und 4709 Bergkamen | Elastisches Klebemittel |
| US4087413A (en) * | 1977-03-07 | 1978-05-02 | The Dow Chemical Company | Crosslinked, linear, acylated polyalkylenepolyamines and process therefor |
| DE3112118A1 (de) * | 1981-03-27 | 1982-10-07 | Bayer Ag, 5090 Leverkusen | Polymerisathaltige polyetherpolyamine, verfahren zur herstellung dieser polyamine und deren verwendung als aufbaukomponente zur herstellung von polyurethanen |
| US4525590A (en) * | 1981-07-29 | 1985-06-25 | Bayer Aktiengesellschaft | Simplified process for the production of polyamines by the alkaline hydrolysis of compounds containing NCO-groups |
| CA1221383A (en) * | 1981-08-07 | 1987-05-05 | Werner Rasshofer | Polyamines, a process for the production of polyamines and their use in the production of polyurethanes |
| US4469857A (en) * | 1981-11-06 | 1984-09-04 | Minnesota Mining And Manufacturing Company | Two component system for the production of a synthetic resin compound capable of curing in the absence of moisture containing a polyisocyanate, a polyenamine, and a carrier compound having water aggregated thereto |
| US4723032A (en) * | 1981-11-12 | 1988-02-02 | Bayer Aktiengesellschaft | Modified polyamines and a process for their production |
| DE3144874A1 (de) * | 1981-11-12 | 1983-05-19 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von polyaminen aus n-monoaryl-n', n'-dialkylharnstoff-verbindungen und ihre verwendung zum aufbau von polyurethanen |
| DE3223398A1 (de) * | 1982-06-23 | 1983-12-29 | Bayer Ag, 5090 Leverkusen | Polyamine, verfahren zur herstellung von polyaminen und deren verwendung zur herstellung von polyurethanen |
| DE3223400A1 (de) * | 1982-06-23 | 1983-12-29 | Bayer Ag, 5090 Leverkusen | Polyamine, verfahren zur herstellung von polyaminen und deren verwendung zur herstellung von polyurethanen |
| DE3223397A1 (de) * | 1982-06-23 | 1983-12-29 | Bayer Ag, 5090 Leverkusen | Einstufenverfahren zur herstellung von polyaminen aus nco-prepolymeren, polyamine und deren verwendung zur herstellung von polyurethanen |
| DE3227219A1 (de) * | 1982-07-21 | 1984-02-02 | Bayer Ag, 5090 Leverkusen | Einstufenverfahren zur herstellung von polyaminen aus nco-praepolymeren, polyamine und deren verwendung zur herstellung von polyurethanen |
| DE3244913A1 (de) * | 1982-12-04 | 1984-06-07 | Bayer Ag, 5090 Leverkusen | Aminogruppen enthaltende reaktionskomponenten, verfahren zu ihrer herstellung und ihre verwendung |
| DE3446921A1 (de) * | 1984-12-21 | 1986-07-03 | Bayer Ag, 5090 Leverkusen | Neue alkoxylierte aminopolyether, verfahren zu ihrer herstellung und sie enthaltende kohle-wasser-aufschlaemmungen |
| DE3530476A1 (de) * | 1985-08-27 | 1987-03-05 | Bayer Ag | Polyamine, verfahren zu ihrer herstellung aus nco-prepolymeren und ihre verwendung bei der herstellung von polyurethanen |
| DE3534947A1 (de) * | 1985-10-01 | 1987-04-09 | Bayer Ag | Verfahren zur herstellung von polyaminen, polyamine und deren verwendung zur herstellung von polyurethanen |
| AT385047B (de) * | 1986-05-27 | 1988-02-10 | Vianova Kunstharz Ag | Verfahren zur herstellung von kationischen wasserverduennbaren bindemitteln und deren verwendung |
| US4966954A (en) * | 1987-03-04 | 1990-10-30 | Rensselaer Polytechnic Institute | Production and processing of thermally stable polyenaminonitriles and polyaminoquinolines therefrom |
| US5053478A (en) * | 1987-03-04 | 1991-10-01 | Moore James A | Production and processing of thermally stable polyenaminonitriles |
| US5072026A (en) * | 1987-03-11 | 1991-12-10 | Ici Americas Inc. | Polyureas by reaction injection moulding of enamino-functional aliphatic polyether resin-containing systems and an enamine-terminated polyether |
| US4935460A (en) * | 1987-03-11 | 1990-06-19 | Ici Americas Inc. | Reaction injection molding compositions |
| US5093383A (en) * | 1987-03-11 | 1992-03-03 | Ici Americas Inc. | Polyurethane/urea foams from isocyanate prepolymers and isocyanate reactive imino/enamino functional reactants |
| GB8821181D0 (en) * | 1988-09-09 | 1988-10-12 | Ici America Inc | Improved reaction injection moulding compositions |
| DE3710432A1 (de) * | 1987-03-28 | 1988-10-06 | Basf Ag | Polyamid- und polyharnstoffgruppen gebunden enthaltende elastomere sowie verfahren zur herstellung von elastischen, kompakten oder zelligen formkoerpern hieraus |
| DE3713858A1 (de) * | 1987-04-25 | 1988-11-17 | Bayer Ag | Aromatische polyamine, ein verfahren zu ihrer herstellung und ihre verwendung zur herstellung von polyurethankunststoffen |
| GB8821186D0 (en) * | 1988-09-09 | 1988-10-12 | Ici America Inc | Compositions of matter |
| GB8821183D0 (en) * | 1988-09-09 | 1988-10-12 | Ici America Inc | Composition of matter |
| GB8924127D0 (en) * | 1989-10-26 | 1989-12-13 | Ici Plc | Compositions of matter |
| US5108575A (en) * | 1990-02-23 | 1992-04-28 | E. I. Du Pont De Nemours And Company | Polyamine enamine containing cationic resin |
| US4980398A (en) * | 1990-02-23 | 1990-12-25 | E. I. Du Pont De Nemours And Company | Polyamine enamine containing cationic resin |
| GB9117068D0 (en) * | 1991-08-08 | 1991-09-25 | Ici Plc | Cold curable polyisocyanate adhesive and sealant systems |
| US5584958A (en) * | 1992-08-04 | 1996-12-17 | Imperial Chemical Industries Plc | Polyisocyanate adhesive and sealant systems |
| US6103849A (en) * | 1994-06-27 | 2000-08-15 | Bayer Corporation | Storage stable, heat curable polyurethane compositions |
| EP1404732B1 (en) * | 2001-06-15 | 2007-07-25 | Huntsman Petrochemical Corporation | Synergistic amine chain-extenders in polyurea spray elastomers |
| EP1854817A1 (de) * | 2006-05-09 | 2007-11-14 | Sika Technology AG | Zweikomponentige Polyurethanzusammensetzung mit hoher Frühfestigkeit |
| CN101687972B (zh) * | 2007-06-19 | 2012-12-19 | 亨斯迈石油化学有限责任公司 | 用于聚氨酯泡沫体的反应性胺催化剂 |
| US20110040016A1 (en) * | 2008-04-21 | 2011-02-17 | Yakulis Jr George | Curable compositions that form a high modulus polyurea |
| US20100152407A1 (en) * | 2008-12-17 | 2010-06-17 | Loctite (R&D) Limited | Novel compounds |
| US20100311890A1 (en) * | 2009-06-05 | 2010-12-09 | Ppg Industries Ohio, Inc. | Curable compositions that form a low modulus polyurea |
| US20110076485A1 (en) * | 2009-09-29 | 2011-03-31 | Ppg Industries Ohio, Inc. | Substrates coated with clear polyurea film-forming compositions |
| BR112013013306A8 (pt) * | 2010-12-03 | 2017-10-10 | Dow Agrosciences Llc | Processos para a preparação de enaminas |
| US20120142944A1 (en) * | 2010-12-03 | 2012-06-07 | Dow Agrosciences Llc | Processes for the preparation of enamines |
| PL2675797T3 (pl) * | 2010-12-03 | 2016-09-30 | Sposoby wytwarzania enamin | |
| CN110360467A (zh) | 2013-04-19 | 2019-10-22 | 科思创有限公司 | 模内电子印刷电路板封装及组件 |
| EP3372624A1 (en) | 2017-03-06 | 2018-09-12 | Henkel AG & Co. KGaA | One component composition based on compounds with at least two exo-vinylene cyclic carbonate units |
| CA3130537A1 (en) * | 2019-02-18 | 2020-08-27 | Basf Se | Process for removal of acid gases from a fluid stream with a liquid absorbent comprising a piperazine ring |
| CN111072903B (zh) * | 2019-12-30 | 2021-04-09 | 中国科学院山西煤炭化学研究所 | 一种阳离子型水性聚氨酯乳液的制备方法 |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1031917A (en) | 1963-12-16 | 1966-06-02 | Wyandotte Chemicals Corp | Polyurethane coating composition |
| GB1064841A (en) * | 1963-02-04 | 1967-04-12 | Ici Ltd | Manufacture of polymers containing biuret and urea groups |
| GB1073209A (en) * | 1965-06-01 | 1967-06-21 | Gen Mills Inc | Improvements in or relating to polyureas |
| FR1493879A (fr) * | 1965-09-17 | 1967-09-01 | Gen Mills Inc | Dérivés de certains polyamines et isocyanates organiques et leur utilisation dans des préparations de polymères |
| US3493543A (en) * | 1967-03-20 | 1970-02-03 | Gen Mills Inc | Polyurea compositions and the coating of substrates with such compositions |
| GB1200718A (en) * | 1968-01-02 | 1970-07-29 | Bayer Ag | Process for the production of crosslinked synthetic resins and sheets produced therefrom |
| US3523925A (en) * | 1966-10-24 | 1970-08-11 | Gen Mills Inc | Polymers prepared from organic polyisocyanates or polyisothiocyanates and amides of certain ketimine blocked polyamines and carboxylic acids |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3074940A (en) * | 1958-09-10 | 1963-01-22 | Monsanto Chemicals | Process for the manufacture of enamines |
| CH372041A (de) * | 1958-09-10 | 1963-09-30 | Monsanto Chemicals | Verfahren zur Herstellung von Isobutenylaminen |
| DE1158496B (de) * | 1961-01-20 | 1963-12-05 | Bayer Ag | Verfahren zur Herstellung von N, N', N'-trisubstituierten p-Phenylendiaminen |
| US3314922A (en) * | 1961-08-21 | 1967-04-18 | Du Pont | Polymers and process of making same |
| DE1226585B (de) * | 1964-09-04 | 1966-10-13 | Bayer Ag | Verfahren zur Herstellung von 1, 3-Dioxanen |
| DE1719121C3 (de) * | 1967-11-04 | 1980-07-10 | Bayer Ag, 5090 Leverkusen | Verfahren zum Abdichten und Ausfüllen von Fugen |
| DE2402037B1 (de) * | 1974-01-17 | 1975-05-28 | Teroson Gmbh, 6900 Heidelberg | Polyvinylchloridplastisole |
-
1971
- 1971-04-06 DE DE2125247A patent/DE2125247C3/de not_active Expired
- 1971-04-06 DE DE2116882A patent/DE2116882C3/de not_active Expired
-
1972
- 1972-04-03 US US240762A patent/US3865791A/en not_active Expired - Lifetime
- 1972-04-05 FR FR7211899A patent/FR2136178A5/fr not_active Expired
- 1972-04-05 AT AT200274*1A patent/AT324513B/de not_active IP Right Cessation
- 1972-04-05 SE SE7204389A patent/SE405256B/xx unknown
- 1972-04-05 AT AT291372A patent/AT329016B/de not_active IP Right Cessation
- 1972-04-06 BE BE781756A patent/BE781756A/xx not_active IP Right Cessation
- 1972-04-06 NL NLAANVRAGE7204634,A patent/NL171816C/xx not_active IP Right Cessation
- 1972-04-06 GB GB1589972A patent/GB1394732A/en not_active Expired
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1064841A (en) * | 1963-02-04 | 1967-04-12 | Ici Ltd | Manufacture of polymers containing biuret and urea groups |
| DE1520139A1 (de) | 1963-02-04 | 1970-03-19 | Ici Ltd | Verfahren zur Herstellung von Polymeren |
| GB1031917A (en) | 1963-12-16 | 1966-06-02 | Wyandotte Chemicals Corp | Polyurethane coating composition |
| GB1073209A (en) * | 1965-06-01 | 1967-06-21 | Gen Mills Inc | Improvements in or relating to polyureas |
| FR1493879A (fr) * | 1965-09-17 | 1967-09-01 | Gen Mills Inc | Dérivés de certains polyamines et isocyanates organiques et leur utilisation dans des préparations de polymères |
| US3523925A (en) * | 1966-10-24 | 1970-08-11 | Gen Mills Inc | Polymers prepared from organic polyisocyanates or polyisothiocyanates and amides of certain ketimine blocked polyamines and carboxylic acids |
| US3493543A (en) * | 1967-03-20 | 1970-02-03 | Gen Mills Inc | Polyurea compositions and the coating of substrates with such compositions |
| GB1200718A (en) * | 1968-01-02 | 1970-07-29 | Bayer Ag | Process for the production of crosslinked synthetic resins and sheets produced therefrom |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1394732A (en) | 1975-05-21 |
| DE2125247B2 (de) | 1977-08-11 |
| US3865791A (en) | 1975-02-11 |
| DE2116882C3 (de) | 1985-05-15 |
| BE781756A (fr) | 1972-10-06 |
| AT329016B (de) | 1976-04-26 |
| ATA291372A (de) | 1975-07-15 |
| DE2116882A1 (de) | 1972-12-07 |
| NL171816B (nl) | 1982-12-16 |
| NL171816C (nl) | 1983-05-16 |
| DE2125247A1 (de) | 1972-10-19 |
| AT324513B (de) | 1975-09-10 |
| DE2116882B2 (de) | 1976-11-25 |
| NL7204634A (enExample) | 1972-10-10 |
| SE405256B (sv) | 1978-11-27 |
| FR2136178A5 (enExample) | 1972-12-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2125247C3 (de) | Verfahren zum Applizieren von Lacken, Vergußmassen, Spachtelmassen, Überzugs- und Beschichtungsmassen | |
| EP0153579B1 (de) | Verwendung von hitzehärtbaren Polyurethanharnstoff-Reaktiv-Klebstoffmassen | |
| DE2131299C3 (de) | Durch Hitzeeinwirkung härtbare Gemische und Verfahren zur Herstellung von Formkörpern aus diesen Gemischen | |
| EP0239834A1 (de) | Feuchtigkeitshärtende, lagerstabile Einkomponenten-Polyurethansysteme und deren Verwendung | |
| DE19701835A1 (de) | Kalthärtende, lösemittelarme oder lösemittelfreie Zweikomponenten-Polyurethan-Polyharnstoff-Massen | |
| CH619474A5 (enExample) | ||
| DE1088641B (de) | Verfahren zum Verkleben von gegossenen Polyurethan-polymerisaten mit Metall | |
| DE1109881B (de) | Verfahren zur Herstellung von Urethangruppen aufweisenden Schaumstoffen | |
| DE1769089B2 (de) | Verfahren zur Herstellung von, gegebenenfalls mikroporösen, Formkörpern | |
| DE69521192T2 (de) | Beschichtungszusammensetzungen auf der Basis von Aldiminen und Uretdiongruppen enthaltenden Polyisocyanaten | |
| DE2739313A1 (de) | Cycloaminale, ein verfahren zu ihrer herstellung, sowie ihre verwendung | |
| EP0477488A1 (de) | Kalthärtende, lösemittelfreie, duroplastische Polyurethan-Polyharnstoff-Massen | |
| DE1057334B (de) | Verfahren zur Herstellung von stickstoffhaltigen polymeren Verbindungen | |
| EP0118821B1 (de) | Verfahren zur Herstellung von Kombinationen aus organischen Polyisocyanaten und zumindest teilweise blockierten Polyaminen, die nach dem Verfahren erhältlichen Kombinationen und ihre Verwendung zur Herstellung von Lacken, Beschichtungs- oder Dichtungsmassen | |
| DE1105157B (de) | Verfahren zur Herstellung von hochmolekularen vernetzten Kunststoffen aus Saeurehydraziden und Isocyanaten | |
| DE2521841C2 (de) | Verfahren zum Abdichten und Ausfüllen von Fugen und zum Beschichten von Oberflächen | |
| US4328330A (en) | Process for the production of polyureas | |
| EP0326512A1 (de) | Härtbares Gemisch | |
| DE1719121C3 (de) | Verfahren zum Abdichten und Ausfüllen von Fugen | |
| DE3306373A1 (de) | Feuchtigkeitshaertendes, lagerstabiles einkomponenten-polyurethansystem | |
| DE10235481A1 (de) | Härtbare Harzmasse | |
| EP0475003A1 (de) | Blockierte (cyclo)-aliphatische Polyisocyanate sowie ein Verfahren zu deren Herstellung | |
| DE2736799A1 (de) | Verfahren zur polymerisation einer urethanbildenden zubereitung | |
| DE69526633T2 (de) | Auf 2-methyl-1,5-pentandiamin basierenden Aldiminen und ihre Verwendung zur Herstellung von Polyharnstoffbeschichtungen | |
| DE2167141C1 (de) | Verfahren zum Applizieren von Lacken,Vergussmassen,Spachtelmassen,UEberzugs- und Beschichtungsmassen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| BI | Miscellaneous see part 2 | ||
| BHJ | Nonpayment of the annual fee | ||
| OI | Miscellaneous see part 1 | ||
| BI | Miscellaneous see part 2 | ||
| C3 | Grant after two publication steps (3rd publication) | ||
| AG | Has addition no. |
Ref country code: DE Ref document number: 2167141 Format of ref document f/p: P |
|
| AH | Division in |
Ref country code: DE Ref document number: 2167141 Format of ref document f/p: P |
|
| AG | Has addition no. |
Ref country code: DE Ref document number: 2167058 Format of ref document f/p: P |
|
| AH | Division in |
Ref country code: DE Ref document number: 2167058 Format of ref document f/p: P |
|
| AG | Has addition no. |
Ref country code: DE Ref document number: 2167059 Format of ref document f/p: P |
|
| AH | Division in |
Ref country code: DE Ref document number: 2167059 Format of ref document f/p: P |
|
| 8339 | Ceased/non-payment of the annual fee |