Poon Kam C, Smith Madeleine L, Williams Charlotte K
Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford OX1 3TA, United Kingdom.
Macromolecules. 2024 Apr 24;57(9):4199-4207. doi: 10.1021/acs.macromol.4c00455. eCollection 2024 May 14.
Using CO polycarbonates as engineering thermoplastics has been limited by their mechanical performances, particularly their brittleness. Poly(cyclohexene carbonate) (PCHC) has a high tensile strength (40 MPa) but is very brittle (elongation at break <3%), which limits both its processing and applications. Here, well-defined, high molar mass CO terpolymers are prepared from cyclohexene oxide (CHO), cyclopentene oxide (CPO), and CO by using a Zn(II)Mg(II) catalyst. In the catalysis, CHO and CPO show reactivity ratios of 1.53 and 0.08 with CO, respectively; as such, the terpolymers have gradient structures. The poly(cyclohexene carbonate)--poly(cyclopentene carbonate) (PCHC--PCPC) have high molar masses (86 < < 164 kg mol, < 1.22) and good thermal stability ( > 250 °C). All the polymers are amorphous with a single, high glass transition temperature (96 < < 108 °C). The polymer entanglement molar masses, determined using dynamic mechanical analyses, range from 4 < < 23 kg mol depending on the polymer composition (PCHC:PCPC). These polymers show superior mechanical performance to PCHC; specifically the lead material (PCHC--PCPC) shows 25% greater tensile strength and 160% higher tensile toughness. These new plastics are recycled, using cycles of reprocessing by compression molding (150 °C, 1.2 ton m, 60 min), four times without any loss in mechanical properties. They are also efficiently chemically recycled to selectively yield the two epoxide monomers, CHO and CPO, as well as carbon dioxide, with high activity (TOF = 270-1653 h, 140 °C, 120 min). The isolated recycled monomers are repolymerized to form thermoplastic showing the same material properties. The findings highlight the benefits of the terpolymer strategy to deliver thermoplastics combining the beneficial low entanglement molar mass, high glass transition temperatures, and tensile strengths; PCHC properties are significantly improved by incorporating small quantities (23 mol %) of cyclopentene carbonate linkages. The general strategy of designing terpolymers to include chain segments of low entanglement molar mass may help to toughen other brittle and renewably sourced plastics.
将一氧化碳基聚碳酸酯用作工程热塑性塑料一直受到其机械性能的限制,尤其是脆性。聚(环己烯碳酸酯)(PCHC)具有较高的拉伸强度(40兆帕),但非常脆(断裂伸长率<3%),这限制了其加工和应用。在此,通过使用锌(II)镁(II)催化剂,由环氧环己烷(CHO)、环氧环戊烷(CPO)和一氧化碳制备了结构明确、高摩尔质量的一氧化碳三元共聚物。在催化过程中,CHO和CPO与一氧化碳的反应比分别为1.53和0.08;因此,三元共聚物具有梯度结构。聚(环己烯碳酸酯)-聚(环戊烯碳酸酯)(PCHC-PCPC)具有高摩尔质量(86<<164千克/摩尔,<1.22)和良好的热稳定性(>250°C)。所有聚合物均为非晶态,具有单一的高玻璃化转变温度(96<<108°C)。使用动态力学分析测定的聚合物缠结摩尔质量范围为4<<23千克/摩尔,具体取决于聚合物组成(PCHC:PCPC)。这些聚合物表现出优于PCHC的机械性能;特别是主要材料(PCHC-PCPC)的拉伸强度提高了25%,拉伸韧性提高了160%。这些新型塑料可通过压缩模塑(150°C,1.2吨/平方米,60分钟)进行多次再加工循环回收,四次循环后机械性能无任何损失。它们还可以有效地进行化学回收,以高活性(TOF = 270-1653小时,140°C,120分钟)选择性地生成两种环氧化合物单体CHO和CPO以及二氧化碳。分离出的回收单体重新聚合形成具有相同材料性能的热塑性塑料。这些发现突出了三元共聚物策略在提供结合有益的低缠结摩尔质量、高玻璃化转变温度和拉伸强度的热塑性塑料方面的优势;通过引入少量(23摩尔%)的环戊烯碳酸酯键,PCHC的性能得到了显著改善。设计包含低缠结摩尔质量链段的三元共聚物的一般策略可能有助于增韧其他脆性且可再生的塑料。