Biobased Superwetting Cotton Fabric with Self-Healing Capacity and pH-Responsive Wettability Enabled by Dynamic Vitrimer Chemistry for On-Demand Oil/Water Separation
The development of advanced superwetting fabrics for oil/water separation is often hampered by limitations in durability, lack of smart responsiveness, and the use of nonsustainable materials. To address these challenges, this study presents a sustainable and smart superhydrophobic cotton fabric (SHCF) fabricated through a three-step process involving cellulase etching, coating with a biobased epoxy vitrimer (EVD), and grafting of octadecylamine (ODA) via dynamic imine bond exchange. The resulting SHCF exhibits excellent superhydrophobicity (WCA: 157.9°) and remarkable durability against boiling water, solvents, and salt. Importantly, the dynamic imine bonds confer self-healing properties to recover superhydrophobicity after mechanical damage and enable pH-responsive wettability. The SHCF can be switched to a hydrophilic state (dSHCF) under acidic conditions, showing underwater superoleophobicity, and critically, can be fully regenerated to a superhydrophobic state (rSHCF) under alkaline conditions. This pH-responsive wettability allows for on-demand oil/water separation: superhydrophobic SHCF effectively separates heavy oil/water mixtures with high efficiency (>93%), while hydrophilic dSHCF separates light oil/water mixtures with exceptional efficiency (>99%) and high flux. The fabric maintains high performance over multiple cycles, demonstrating its great potential for adaptive and sustainable oil/water separation applications.
Authors
- Min‐Huey Chen (ORCID: https://orcid.org/0000-0002-4853-1906)
- Yong Li (ORCID: https://orcid.org/0000-0003-4038-0493)
- P. B. Li
- Jian-Bing Zeng
- Gao-Can Zhu
Institutions
- Southwest University (CN)
Publication Details
- Journal
- ACS Sustainable Chemistry & Engineering
- Published
- 2026-02-04
- DOI
- https://doi.org/10.1021/acssuschemeng.5c11974
- Primary Topic
- Surface Modification and Superhydrophobicity
- Type
- article
- Field-Weighted Citation Impact
- 0.00