Dual-Functional Biopolyurethane Blends with Shape-Memory and Self-Healing Properties: Effects of Mixed Hard Domains on Structures and Properties AITranslate
Abstract AITranslate
Thermoplastic biopolyurethanes (bio-TPUs) with shape-memory and self-healing properties exhibit promising application in smart medical devices. The phase structure plays a crucial role in designing dual-functional bio-TPUs, and the stability of the hard domain can directly affect the structure and properties of bio-TPUs. It is of high application value to simultaneously optimize the shape-memory and self-healing properties of TPUs by adjusting the composition of the hard domain. In this study, two kinds of TPUs containing either alicyclic isocyanate [isophorone diisocyanate (IPDI)] or aliphatic isocyanate [hexamethylene diisocyanate (HDI)] were prepared, and tunable thermoresponsive shape-memory and self-healing dual-function blends were constructed by solution blending of IPDI-based PU (I-PU) and HDI-based PU (H-PU). Based on the hydrogen bonding between the urethane groups, the two types of hard segments in the blend could self-assemble into mixed hard domains, and the phase-transition temperature of hard domains could be increased from 130 to 163 °C with the addition of H-PU. It is worth noting that the self-assembly of the hard segments weakened the effect on the chain motion of the soft segments, resulting in an increased crystallized ability of the soft segments. Hence, the shape-memory behavior of the blends could be modified according to the H-PU content. The increase of the H-PU content decreased the shape fixity (100–93.1%) and recovery ratios (96.2–76.7%) of the blends but increased the stability of the shape-memory process. Meanwhile, the mixed hard domains served as the stationary phase, and the chain motion of the soft segments at 60 °C imparted self-healing properties to the blends. Combined with excellent biocompatibility, the designed blends are promising to be used in various cutting-edge applications, such as tissue scaffolds, smart clothing, and wearable devices.
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DOI:https://doi.org/10.1021/acsapm.3c01865
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Thermoplastic biopolyurethanes (bio-TPUs) with shape-memory and self-healing properties exhibit promising application in smart medical devices. The phase structure plays a crucial role in designing dual-functional bio-TPUs, and the stability of the hard domain can directly affect the structure and properties of bio-TPUs. It is of high application value to simultaneously optimize the shape-memory and self-healing properties of TPUs by adjusting the composition of the hard domain. In this study, two kinds of TPUs containing either alicyclic isocyanate [isophorone diisocyanate (IPDI)] or aliphatic isocyanate [hexamethylene diisocyanate (HDI)] were prepared, and tunable thermoresponsive shape-memory and self-healing dual-function blends were constructed by solution blending of IPDI-based PU (I-PU) and HDI-based PU (H-PU). Based on the hydrogen bonding between the urethane groups, the two types of hard segments in the blend could self-assemble into mixed hard domains, and the phase-transition temperature of hard domains could be increased from 130 to 163 °C with the addition of H-PU. It is worth noting that the self-assembly of the hard segments weakened the effect on the chain motion of the soft segments, resulting in an increased crystallized ability of the soft segments. Hence, the shape-memory behavior of the blends could be modified according to the H-PU content. The increase of the H-PU content decreased the shape fixity (100–93.1%) and recovery ratios (96.2–76.7%) of the blends but increased the stability of the shape-memory process. Meanwhile, the mixed hard domains served as the stationary phase, and the chain motion of the soft segments at 60 °C imparted self-healing properties to the blends. Combined with excellent biocompatibility, the designed blends are promising to be used in various cutting-edge applications, such as tissue scaffolds, smart clothing, and wearable devices.
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| GB/T 7714-2015 | [1] Yujie Wang, Huifang Nie, Shimin Wang, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.3c01865. |
| MLA | [1] Yujie Wang, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.3c01865. |
| APA | [1] Yujie Wang, Huifang Nie, Shimin Wang, Hao Zhang, Xiaofeng Zhang, Lei Jiang, Wentao Liu, & Miaoming Huang. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.3c01865 |
| IEEE | [1] Yujie Wang, Huifang Nie, Shimin Wang, Hao Zhang, Xiaofeng Zhang, Lei Jiang, Wentao Liu, and Miaoming Huang, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.3c01865. keywords: {TPU blends;tunable microphase structure;stimulusresponse;shapememory property;selfhealing;biomaterials} |
