Dynamic Hydrophobic Domains Enable the Fabrication of Mechanically Robust and Highly Elastic Poly(vinyl alcohol)-Based Hydrogels with Excellent Self-Healing Ability AITranslate
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It is a great challenge to fabricate self-healing hydrogels that simultaneously possess high mechanical strength and good elasticity, and are capable of rapidly and efficiently healing physical damage. In this work, such hydrogels are fabricated by grafting 4-carboxybenzaldehyde (CBA) onto poly(vinyl alcohol) (PVA) in dimethyl sulfoxide, followed by sequential dialysis in ethanol and water. The dialysis in ethanol generates hydrogen-bond-cross-linked PVA-CBA organogels with homogeneous structures while the subsequent dialysis in water leads to PVA-CBA hydrogels uniformly dispersed with hydrogen-bond-cross-linked hydrophobic domains. The in-situ-formed hydrophobic domains with an average diameter of ∼13 nm can strengthen the PVA-CBA hydrogels to a tensile strength of ∼5.8 MPa and toughness of ∼14.9 MJ m–3, and endow the hydrogels with good elasticity. Because of the presence of hydrogen bonds, the hydrophobic domains can reversibly break and reform to enable the rapid and efficient self-healing of fractured hydrogels at room temperature to restore their original mechanical strength. Meanwhile, the hydrogels have good biocompatibility and are potentially useful as post-operative antiadhesive films.
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DOI:https://doi.org/10.1021/acsmaterialslett.0c00075
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It is a great challenge to fabricate self-healing hydrogels that simultaneously possess high mechanical strength and good elasticity, and are capable of rapidly and efficiently healing physical damage. In this work, such hydrogels are fabricated by grafting 4-carboxybenzaldehyde (CBA) onto poly(vinyl alcohol) (PVA) in dimethyl sulfoxide, followed by sequential dialysis in ethanol and water. The dialysis in ethanol generates hydrogen-bond-cross-linked PVA-CBA organogels with homogeneous structures while the subsequent dialysis in water leads to PVA-CBA hydrogels uniformly dispersed with hydrogen-bond-cross-linked hydrophobic domains. The in-situ-formed hydrophobic domains with an average diameter of ∼13 nm can strengthen the PVA-CBA hydrogels to a tensile strength of ∼5.8 MPa and toughness of ∼14.9 MJ m–3, and endow the hydrogels with good elasticity. Because of the presence of hydrogen bonds, the hydrophobic domains can reversibly break and reform to enable the rapid and efficient self-healing of fractured hydrogels at room temperature to restore their original mechanical strength. Meanwhile, the hydrogels have good biocompatibility and are potentially useful as post-operative antiadhesive films.
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| GB/T 7714-2015 | [1] Xu Fang, Yixuan Li, Xiang Li, et al. ACS Materials Letters, 2020(2). DOI:10.1021/acsmaterialslett.0c00075. |
| MLA | [1] Xu Fang, et al., ACS Materials Letters, no. 2, 2020, https://doi.org/10.1021/acsmaterialslett.0c00075. |
| APA | [1] Xu Fang, Yixuan Li, Xiang Li, Wenmo Liu, Xianghui Yu, Fei Yan, & Junqi Sun. (2020). ACS Materials Letters(2). https://doi.org/10.1021/acsmaterialslett.0c00075 |
| IEEE | [1] Xu Fang, Yixuan Li, Xiang Li, Wenmo Liu, Xianghui Yu, Fei Yan, and Junqi Sun, ACS Materials Letters, no. 2, 2020, doi: 10.1021/acsmaterialslett.0c00075. |
