Abstract: The present invention relates to a process for producing 2-(2,2,6,6-tetramethylpiperidin-4-yl)propane-1,3-diamine, which can be used as hardener in epoxide applications.

Abstract: A process for producing 2-(2,2,6,6-tetramethylpiperidin-4-yl)propane-1,3-diamine by A) reacting triacetonamine (TAA) and malononitrile to afford the intermediate 2-(2,2,6,6-tetramethylpiperidin-4-ylidene)malononitrile, and B) hydrogenating 2-(2,2,6,6-tetramethylpiperidin-4-ylidene)malononitrile in the presence of at least one catalyst. In another embodiment, the hydrogenation in step B) of the process is performed at 20-120° C. and at 20-300 bar. In another embodiment, the hydrogenation in step B) of the process is performed in two stages at 20-120° C. and at 20-300 bar.

Abstract: A diamine 2-(3,3,5-trimethylcyclohexyl)propane-1,3-diamine of formula 1 and a process for producing 2-(3,3,5-trimethylcyclohexyl)propane-1,3-diamine by A) reacting isophorone (IP) and malononitrile to afford the intermediate 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile, and B) hydrogenating 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile in the presence of at least one catalyst. In another embodiment, the hydrogenation in step B) of the process is performed at 20-120° C. and at 20-300 bar.

Abstract: The present invention is directed to a reinforced building block made of autoclaved aerated concrete (AAC) comprising rebars formed essentially from A) at least one fibrous carrier and B) and a hardened composition formed from B1) at least one epoxy compound and B2) at least one diamine and/or polyamine in a stoichiometric ratio of the epoxy compound B1) to the diamine and/or polyamine component B2) of 0.

Abstract: An epoxy resin composition including A) at least one epoxy compound and B) a hardener composition including B1) 0.1%-100% by weight of 2-(3-(aminomethyl)-3,5,5-trimethylcyclohexyl)propane-1,3-diamine, and B2) 99.9%-0% by weight of at least one further diamine and/or polyamine, where the stoichiometric ratio of the epoxy groups of A) and the number of active hydrogen atoms of the functional groups of B) varies from 1:2 to 2:1.

Abstract: An epoxy resin composition including A) at least one epoxy compound, and B) a hardener composition including B1) from 0.1%-100% by weight of 2-(3,3,5-trimethylcyclohexyl)propane-1,3-diamine, and B2) from 99.9%-0% by weight of at least one further diamine and/or polyamine, where the stoichiometric ratio of the epoxy groups of A) and the number of active hydrogen atoms of the functional groups of B) varies from 1:2 to 2:1.

Abstract: An epoxy resin composition including A) at least one epoxy compound, and B) a hardener composition including B1) from 0.1%-100% by weight of 2-(2,2,6,6-tetramethylpiperidin-4-yl)propane-1,3-diamine, and B2) from 99.9%-0% by weight of at least one further diamine and/or polyamine, where the stoichiometric ratio of the epoxy groups of A) and the number of active hydrogen atoms of the functional groups of B) varies from 1:2 to 2:1.

Abstract: A compound of the structural formula 1 Also disclosed is a process for producing 2-(3-(aminomethyl)-3,5,5-trimethylcyclohexyl)propane-1,3-diamine by A) reacting isophorone nitrile and malononitrile to afford the intermediate 2-(3-cyano-3,5,5-trimethylcyclohexylidene)malononitrile, and B) hydrogenating 2-(3-cyano-3,5,5-trimethylcyclohexylidene)malononitrile in the presence of at least one catalyst. In another embodiment, the hydrogenation in step B) of the process is performed at 20-120° C. and at 20-300 bar.

Abstract: A process for producing 2-(2,2,6,6-tetramethylpiperidin-4-yl)propane-1,3-diamine by A) reacting triacetonamine (TAA) and malononitrile to afford the intermediate 2-(2,2,6,6-tetramethylpiperidin-4-ylidene)malononitrile, and B) hydrogenating 2-(2,2,6,6-tetramethylpiperidin-4-ylidene)malononitrile in the presence of at least one catalyst. In another embodiment, the hydrogenation in step B) of the process is performed at 20-120° C. and at 20-300 bar. In another embodiment, the hydrogenation in step B) of the process is performed in two stages at 20-120° C. and at 20-300 bar.

Abstract: A diamine 2-(3,3,5-trimethylcyclohexyl)propane-1,3-diamine of formula 1 and a process for producing 2-(3,3,5-trimethylcyclohexyl)propane-1,3-diamine by A) reacting isophorone (IP) and malononitrile to afford the intermediate 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile, and B) hydrogenating 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile in the presence of at least one catalyst. In another embodiment, the hydrogenation in step B) of the process is performed at 20-120° C. and at 20-300 bar.

Abstract: Epoxy compositions containing at least one resin component and at least one hardener component, are suitable as a thermoset matrix for production of semi-finished fibre matrix products and cured fibre matrix laminates.

Abstract: Epoxy resin compositions containing at least one resin component and at least one hardener component are suitable as a thermoset matrix for production of semi-finished fibre matrix products and cured fibre matrix laminates known as composites.

Abstract: The invention relates to curable compositions comprising at least one epoxy resin and at least one hardener wherein the hardener is a compound of formula (I) or (II) where R1 and R2 are each independently selected from the group of substituents having the formula —(CH2)x—NH2 and x is in each case independently 0, 1, 2, 3 or 4, to surfaces comprising such compositions, to methods comprising applying a coating material comprising such compositions and to the use of such compositions as surface protection.

Abstract: The present invention relates to a curable or hardened composition comprising at least one epoxy resin, one open-chain polyamine and one compound of the formula (I) where the moieties R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19 and R20 respectively and mutually independently are selected from the group comprising hydrogen, methyl, ethyl, propyl, isopropyl and amine, with the proviso that at least one moiety from the group comprising R1, R2, R3, R4, R5, R6, R7, R8, R9 and R10 is amine and at least one moiety from the group comprising R11, R12, R13, R14, R15, R16, R17, R18, R19 and R20 is amine; to use of a hardener combination comprising an aliphatic diamine and a compound of the formula (I) for the curing of epoxy resin; to a process for the coating of a surface or for the impregnation of a textile sheet, comprising the steps of (a) application and (b) hardening of the curable composition, and also to a surface, fibre composite material, coating or adhesive compri

Abstract: The present invention relates to the use of substituted benzyl alcohols as modifiers in epoxy systems.

Abstract: The invention relates to curable compositions comprising at least one epoxy resin and at least one hardener wherein the hardener is a compound of formula (I) or (II) where R1 and R2 are each independently selected from the group of substituents having the formula —(CH2)x—NH2 and x is in each case independently 0, 1, 2, 3 or 4, to surfaces comprising such compositions, to methods comprising applying a coating material comprising such compositions and to the use of such compositions as surface protection.

Abstract: The invention relates to a method for producing storage-stable polyurethane prepregs and molding bodies produced therefrom (composite components), which can be obtained by a method using a polyurethane composition in solution and by impregnation of fibre-reinforced materials such as of woven fabrics and laid scrim using reactive polyurethane compositions.

Abstract: The invention relates to curable compositions substantially comprising A) at least one epoxy resin, and B) at least one curing agent comprising a hetero-poly-cyclic ring system comprising at least two amino groups.