Five secondary amine terminated poly（ester-amine）s （defined as PEA） with controlled molecular structures were synthesized through reacting excessive piperazine with phthalicdiglycol diacrylate （PDDA） and 1,1,1-t...Five secondary amine terminated poly（ester-amine）s （defined as PEA） with controlled molecular structures were synthesized through reacting excessive piperazine with phthalicdiglycol diacrylate （PDDA） and 1,1,1-trimethylolpropane triacrylate （TMPTA） at a constant secondary amine/acrylate group ratio of 1.5/1 and at different PDDA/TMPTA molar ratios. Both IR and ^1H-NMR spectra indicated that all acrylate groups were consumed in the reaction, based on which the structural parameters were calculated from the ^1H-NMR spectra. With decreasing PDDA/TMPTA ratio, the content of secondary amine, degree of branching, molecular weight, Tg and Td increased accordingly. These polymers were further used as both crosslinkers and flexibilizers for a linear epoxy resin E51 to form cured films under ambient condition. The gel content, relative hardness and Tg of the resulting films increased as PEA molecules changed from linear to highly branching structures. Due to the flexibility of PEA molecules, all the films possessed excellent mechanical performance.展开更多
Three secondary amine terminated hyperbranched poly（ester-amine）s （defined as HPEA1, HPEA2 and HPEA3） were synthesized from piperazine （A2） and trimethylolpropane triacrylate （TMPTA, B3） at their molar ratios ...Three secondary amine terminated hyperbranched poly（ester-amine）s （defined as HPEA1, HPEA2 and HPEA3） were synthesized from piperazine （A2） and trimethylolpropane triacrylate （TMPTA, B3） at their molar ratios of 2.5：1, 2.25：1 and 2.0：1, respectively. The polymers were analyzed by 1H NMR, GPC, DSC and TGA. The results indicated that the ratio of secondary amine to tertiary amine and the content of secondary amine decreased, while the molecular weight, molecular weight distribution and glass transition temperature （Tg） increased from HPEA1 to HPEA3. Due to their reactive terminal groups and flexible chains, these polymers further reacted with an epoxy resin （E51） to form cured films under ambient conditions. With increasing the ratio between secondary amine groups and epoxy groups from 1：2 to 2：1, the gel content, film hardness and onset decomposing temperature of the cured samples increased. The good film performances should make the polymers as the components of non-solvent coating materials.展开更多
基金The work was financially supported by the National Science Foundation of China(Nos.20204005,50233030).
文摘Five secondary amine terminated poly（ester-amine）s （defined as PEA） with controlled molecular structures were synthesized through reacting excessive piperazine with phthalicdiglycol diacrylate （PDDA） and 1,1,1-trimethylolpropane triacrylate （TMPTA） at a constant secondary amine/acrylate group ratio of 1.5/1 and at different PDDA/TMPTA molar ratios. Both IR and ^1H-NMR spectra indicated that all acrylate groups were consumed in the reaction, based on which the structural parameters were calculated from the ^1H-NMR spectra. With decreasing PDDA/TMPTA ratio, the content of secondary amine, degree of branching, molecular weight, Tg and Td increased accordingly. These polymers were further used as both crosslinkers and flexibilizers for a linear epoxy resin E51 to form cured films under ambient condition. The gel content, relative hardness and Tg of the resulting films increased as PEA molecules changed from linear to highly branching structures. Due to the flexibility of PEA molecules, all the films possessed excellent mechanical performance.
文摘Three secondary amine terminated hyperbranched poly（ester-amine）s （defined as HPEA1, HPEA2 and HPEA3） were synthesized from piperazine （A2） and trimethylolpropane triacrylate （TMPTA, B3） at their molar ratios of 2.5：1, 2.25：1 and 2.0：1, respectively. The polymers were analyzed by 1H NMR, GPC, DSC and TGA. The results indicated that the ratio of secondary amine to tertiary amine and the content of secondary amine decreased, while the molecular weight, molecular weight distribution and glass transition temperature （Tg） increased from HPEA1 to HPEA3. Due to their reactive terminal groups and flexible chains, these polymers further reacted with an epoxy resin （E51） to form cured films under ambient conditions. With increasing the ratio between secondary amine groups and epoxy groups from 1：2 to 2：1, the gel content, film hardness and onset decomposing temperature of the cured samples increased. The good film performances should make the polymers as the components of non-solvent coating materials.
