Copper-Integrated Aminated/Amidine-Functionalized Acrylic Textile for High-Stability HRP Immobilization and Bisphenol A Removal
This work introduces a textile-based platform for biocatalysis by integrating a copper-based hybrid domain onto aminated/amidine-functionalized acrylic textile (TAC–Cu), producing a functional bio-textile capable of high-performance enzyme immobilization. The textile substrate was chemically modified with ethylenediamine to generate amine/amidine-type functional groups, enabling in situ formation of copper-based hybrid structures through either a conventional solvothermal approach or a plant-mediated route employing Costus speciosus extract. The green-synthesized TAC–Cu composite exhibited superior structural uniformity, improved porosity, and enhanced surface chemistry, resulting in a higher horseradish peroxidase (HRP) immobilization yield (92%) compared with the chemically synthesized analogue. The resulting HRP-functionalized bio-textile demonstrated markedly improved catalytic behavior, including a reaction rate constant nearly twice that of the free enzyme, and strong operational robustness. As a technical textile engineered for environmental applications, the composite achieved 90% bisphenol A (BPA) removal within 90 min and retained substantial enzymatic activity even at 80 °C, whereas free HRP was almost fully deactivated. Overall, this study highlights the potential of eco-engineered TAC–Cu materials as a new class of functional and sustainable bio-textiles, combining enzyme stabilization, high catalytic efficiency, and suitability for wastewater treatment and other technical textile applications.
Authors
- J. Alkabli
- Naif Abdullah R. Almalki (ORCID: https://orcid.org/0000-0002-1142-607X)
- Yaaser Q. Almulaiky (ORCID: https://orcid.org/0000-0002-8934-8358)
Institutions
- King Abdulaziz University (SA)
- University of Jeddah (SA)
Publication Details
- Journal
- Polymers
- Published
- 2026-05-31
- DOI
- https://doi.org/10.3390/polym18111364
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 0.00