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

机译:低粘度无有机锡可湿固化的硅烷封端的聚氨基甲酸乙酯-尿烷的合成

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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低粘度可湿固化的硅烷封端的聚(氨基甲酸酯-脲)(SPUR)的可能性。首先,制备NCO端基的氨基甲酸酯预聚物,然后进行硅烷封端。考察了多元醇分子量和异氰酸酯与多元醇的比例(NCO / OH)对粘度和SPUR性能的影响。作为传统上用于聚氨酯合成和固化工艺的有机锡催化剂的替代品,已评估了羧酸铋催化剂。此外,有机官能团在氨基硅烷结构(R1-NH-R2-Si(OR3)3)中的作用,即R1(烷基,芳基或三甲氧基甲硅烷基-丙基),间隔基R2(α或γ)和烷基检查了R 3(甲基或乙基)。通过核磁共振波谱(NMR),傅里叶变换红外光谱(FT-IR)研究了SPUR的化学和物理结构,并通过拉伸试验评估了机械性能。结果表明,可以成功地合成硅烷封端的可湿固化的聚氨酯,并用羧酸铋铋催化剂进行固化。通过使用具有高金属含量(19%–21%)的环境友好的羧酸铋铋催化剂,可以通过使用仲氨基硅烷封端剂以及多元醇分子量和NCO的最佳组合来制备具有低粘度,具有足够的拉伸强度和伸长率的SPUR, / OH比。

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