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Non-Isocyanate and Catalyst-Free Synthesis of a Recyclable Polythiourethane with Cyclic Structure

机译:具有环状结构的非异氰酸酯和无可回收的聚噻吩的无可核化合成

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Polythiourethane is a promising heteroatom-containing polymeric material possessing outstanding properties such as high refractive index, biocompatibility, and good coordinating ability to heavy metal ions. However, examples of versatile polythiourethanes are relatively scarce as a result of the limited methods for their synthesis. Herein, we report an efficient non-isocyanate and catalyst-free strategy to synthesize polythiourethane from the highly alternating and regioselective copolymerization of carbonyl sulfide (COS) and 2-methyl aziridine. The copolymerization proceeded efficiently at room temperature and afforded copolymer in 95% selectivity and molecular weight of 15.2 kg/mol in 2 h. Furthermore, the reaction was efficient even at 1 atm of COS at room temperature. Remarkably, the copolymer possessed a cyclic topology, and it could be completely recycled into cyclic thiourethane by simply heating the bulk materials at 200 degrees C for 1.5 h. The copolymer was applied as a heavy metal absorption and recovery agent; lead ions in aqueous solution were adsorbed by the copolymer, and both were eventually separated and recovered in the form of lead compounds and cyclic thiourethanes, respectively. Hence, this study provides a sustainable and atom-economical method for synthesizing polythiourethane and a green method to recover hazardous metals with minimal waste and VOC emission.
机译:聚噻吩是一种含有含有优异性质的有前途的含杂原子的聚合物材料,例如高折射率,生物相容性和良好的重金属离子的良好配位能力。然而,由于其合成方法有限的方法,多种多噻吩烷的实例相对稀缺。在此,我们报告了一种有效的非异氰酸酯和无异氰酸酯和催化剂的策略,从羰基硫醚(COS)和2-甲基氮丙啶的高度交替和区域选择性共聚合中合成聚噻吩。共聚在室温下有效地进行,并在95%选择性和分子量中得到的共聚物,2小时内为15.2kg / mol。此外,即使在室温下在1atm的COS中也是有效的反应。值得注意的是,共聚物具有循环拓扑,并且可以通过简单地将散装材料以200℃加热1.5小时来完全再循环到环硫醚中。将共聚物用作重金属吸收和回收剂;通过共聚物吸附水溶液中的铅离子,并且两者最终分离并分别以铅化合物和环硫醚形式回收。因此,本研究提供了一种可持续的和原子经济的方法,用于合成聚噻吩甲烷和绿色方法,以通过最小的废物和VOC排放来回收危险金属。

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