Recyclable Covalent Adaptable Polystyrene Networks Using Boronates and TetraAzaADamantanes

被引:0
|
作者
van Hurne, Simon [1 ]
Raut, Sagar Kumar [1 ]
Smulders, Maarten Marinus Johannes [1 ]
机构
[1] Wageningen Univ, Lab Organ Chem, NL-6708 WE Wageningen, Netherlands
关键词
vitrimer; covalent adaptable network; boronicester; polystyrene; recycling; POLYMER NETWORKS; VITRIMERS; THERMOSETS; CHEMISTRY; THERMOPLASTICS; RELAXATION; PLASTICS; ROBUST;
D O I
10.1021/acsapm.4c01633
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
With an ever-increasing annual production of polymers and the accumulation of polymer waste leading to progressively adverse environmental consequences, it has become important that all polymers can be efficiently recycled at the end of their life cycle. Especially thermosets are intrinsically difficult to recycle because of their permanent covalent cross-links. A possible solution is to switch from using thermosets to covalent adaptable networks, sparking the rapid development of novel dynamic covalent chemistries and derived polymer materials. Next to development of these innovative polymer materials, there is also an evident advantage of merging the virtues of covalent adaptable networks with the proven material properties of widely used commodity plastics, by introducing dynamic covalent bonds in these original thermoplastic materials to obtain recyclable thermosets. Here we report the synthesis and characterization of a polystyrene polymer, functionalized with TetraAzaADamantanes and cross-linked with dynamic covalent boronic esters. The material properties were characterized for different degrees of cross-linking. The materials showed good solvent resistance with a high remaining insoluble fraction. In line with the typical behavior of traditional covalent adaptable networks, the prepared polystyrene-based boronate-TetraAzaADamantane materials were able to undergo stress relaxation. The material relaxation was also shown to be tunable by mixing with an acid catalyst. Lastly, the materials could be recycled at least 2 times.
引用
收藏
页码:7918 / 7925
页数:8
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