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Specialty polyurethane soft segments. III. Synthesis and characterization ofN‐isopropyl polyether polyamine oligomers containing backbone urea or amide moieties

机译:特种聚氨酯软质段。三、含骨架脲或酰胺部分的N-异丙基聚醚多胺低聚物的合成与表征

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AbstractPrimary polyether polyamine oligomers containing preformed urea or amide moieties in their backbones were converted to the correspondingN‐isopropyl polyether polyamine oligomers (secondary amines) by reaction with acetone and hydrogen in the presence of a catalyst. The best results were from reactions carried out at about 150°C using a supported platinium or palladium catalyst in a fixed bed. Reactants and products were monitored by quantitative carbon‐13 NMR, size exclusion chromatography, and amine titration. Perchloric acid titration was used to quantify the number of urea moleties per molecule. Amide backbone materials gave very little backbone degradation. However, some backbone degradation was observed with urea backbone materials, leading to products with lower molecular weights. These polyether polyamine oligomers, containing urea or amide moieties in their backbones, are useful in urethane/urea polymer systems. The lower reactivity of these secondary amines (toward polyisocyanates) results in their utility in a broader range of polyurethane fabrication technologies. © 1992 John WileySons
机译:摘要在催化剂存在下,将主链中含有预制尿素或酰胺部分的伯聚醚多胺低聚物与丙酮和氢气反应转化为相应的N-异丙基聚醚多胺低聚物(仲胺)。最好的结果是在约150°C下使用负载铂或钯催化剂在固定床中进行的反应。通过定量碳-13 NMR、体积排阻色谱和胺滴定法监测反应物和产物。使用高氯酸滴定法来量化每个分子的尿素分子数。酰胺主链材料对骨架降解的影响很小。然而,尿素骨架材料观察到一些骨架降解,导致产品分子量较低。这些聚醚多胺低聚物在其主链中含有尿素或酰胺部分,可用于聚氨酯/尿素聚合物体系。这些仲胺(对聚异氰酸酯)的反应性较低,因此在更广泛的聚氨酯制造技术中具有实用性。© 1992 约翰·威利父子

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