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Updated: Sep 26, 2026

Synthesis of Strong Adhesive Hydrogel, Gelatin O-Nitrosobenzaldehyde
Published on: November 11, 2022
Versatile carboxymethyl cellulose-based pH responsive hydrogel with robust mechanical strength, adhesion, and
Durgesh Kumar Sinha1, Nishikanta Singh1, Onkarnath Verma2
1Department of Chemistry, Indian Institute of Technology Bhilai, Durg 491001, Chhattisgarh, India.
Abstract:
Hydrogels exhibiting functional properties like mechanical strength, self-healing ability, strong adhesion, and reliable sensing performance remains a major challenge for wearable electronics. Herein, a sustainable biomass-derived CPAT hydrogel was fabricated from carboxymethyl cellulose (CMC), poly(vinyl alcohol) (PVA), acrylic acid (AA), and tannic acid (TA) through UV-induced polymerization and supramolecular crosslinking. The cooperative integration of a poly(ethylene glycol)diacrylate crosslinked poly(acrylic acid) (PAA-PEGDA) network with dynamic hydrogen-bonding interactions generated a robust multi-network architecture. This material exhibited good stretchability, high tensile strength, and toughness. Furthermore, the hydrogel demonstrated efficient self-healing with a healing efficiency exceeding 90%, an elastic recovery of approximately 90%, and 96% stress retention after repeated deformation cycles. The hydrogel displayed strong universal adhesion, pronounced pH-responsive swelling and sensing behaviour. Electrochemical impedance spectroscopy revealed an ionic conductivity of 3.33 × 10--2 S cm-1, while stable sensing performance was maintained over 1000 loading-unloading cycles. The hydrogel enabled real-time monitoring of human motions and good physiological activities, including swallowing and speech-related throat movements. The material exhibited excellent cytocompatibility, maintaining approximately 93% viability of L929 fibroblast cells. These results show the potential use of CPAT hydrogel as a multifunctional platform for wearable sensors, human-machine interfaces, and intelligent healthcare application.
