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The Synthesis of Low-Viscosity Organotin-Free Moisture-Curable Silane-Terminated Poly(Urethane-Urea)s

机译:低粘度有机素无能水分可固化硅烷封端的聚(氨基甲酸酯 - 脲)的合成

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摘要

This work explores the possibility of synthesizing moisture-curable silane-terminated poly(urethane-urea)s (SPURs) of low viscosity. First, NCO-terminated urethane prepolymers were prepared, followed by silane end-capping. The impact of polyol molecular weight and the ratio of isocyanate to polyol (NCO/OH) on viscosity and the properties of SPUR were examined. As alternatives to the organotin catalysts traditionally used for the polyurethane synthesis and curing processes, bismuth carboxylate catalysts were evaluated. In addition, the effect of organofunctional groups in the aminosilane structure (R1–NH–R2–Si(OR3)3), i.e., R1 (alkyl, aryl or trimethoxysilyl-propyl), the spacer R2 (α or γ) and alkyl group R3 (methyl or ethyl), was examined. The chemical and physical structures of the SPUR were investigated by nuclear magnetic resonance spectroscopy (NMR), Fourier transform infrared spectroscopy (FT-IR) and the mechanical properties were evaluated by tensile tests. The results reveal that silane-terminated, moisture-curable polyurethanes can be successfully synthesized and cured with bismuth carboxylate catalysts. SPUR exhibiting low viscosity, with adequate tensile strength and elongation can be prepared using environmentally benign bismuth carboxylate catalyst having a high metal content of 19%–21%, by utilizing secondary aminosilane end-cappers and an optimal combination of the polyol molecular weight and NCO/OH ratio.
机译:这项工作探讨了合成含水性可固化的硅烷封端的聚(氨基甲酸酯 - 脲)S(氨基氨基脲)S(马刺)的可能性。首先,制备NCO封端的氨基甲酸酯预聚物,然后是硅烷末端封端。研究了多元醇分子量的影响和异氰酸酯与多元醇(NCO / OH)对粘度的影响和施用的性质。作为传统上用于聚氨酯合成和固化方法的有机锡催化剂的替代品,评价铋羧酸铋催化剂。此外,有机偶联基团在氨基硅烷结构中的影响(R1-NH-R2-Si(OR 3),即R1(烷基,芳基或三甲氧基甲硅烷基 - 丙基),间隔物R2(α或γ)和烷基检查R3(甲基或乙基)。通过核磁共振光谱(NMR)研究了旋刺的化学和物理结构,通过拉伸试验评估了傅里叶变换红外光谱(FT-IR)和机械性能。结果表明,硅烷封端的可水分固化的聚氨酯可以成功合成并用羧酸铋催化剂固化。具有足够的抗拉强度和伸长率的浓度具有足够的拉伸强度和伸长率,可以使用高金属含量为19%-21%,利用仲氨基硅烷末端烧点和多元醇分子量和NCO的最佳组合来制备高金属含量为19%-21%的羧酸盐催化剂制备/ OH比率。

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