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In this study, we address the challenge of developing highly conductive hydrogels with enhanced stretchability for use in wearable sensors, which are critical for the precise detection of human motion and subtle physiological strains. Our novel approach utilizes amylopectin, a biopolymer, for the uniform integration of liquid metal gallium into the hydrogel matrix. This integration results in a conductive hydrogel characterized by remarkable elasticity (up to 7100 % extensibility) and superior electrical conductance (Gauge Factor = 31.4), coupled with a minimal detection limit of less than 0.1 % and exceptional durability over 5000 cycles. The hydrogel demonstrates significant antibacterial activity, inhibiting microbial growth in moist environments, thus enhancing its applicability in medical settings. Employing a synthesis process that involves ambient condition polymerization of acrylic acid, facilitated by a hydrophobic associative framework, this hydrogel stands out for its rapid gelation and robust mechanical properties. The potential applications of this hydrogel extend beyond wearable sensors, promising advancements in human-computer interaction through technologies like wireless actuation of robotic systems. This study not only introduces a viable material for current wearable technologies but also sets a foundation for future innovations in bio-compatible sensors and interactive devices., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The conductive hemicellulose hydrogels (CHHs) were achieved by incorporating carboxyl terminated aniline pentamer (CTAP) into the hydrophilic xylan-rich hemicellulose networks with epichlorohydrin. CHHs were obtained by facile one-pot reaction in water at ambient temperature. The successful synthesis of CTAP was confirmed by FT-IR, 1 H NMR, and UV-vis spectra. All the hydrogels reached their equilibrium-swollen state within 12 h. The morphology and the thermal stability of CHHs were adjusted by the addition of CTAP. The conductivities of CHHs could also be tuned from 8.92 × 10 -5 to 2.11 × 10 -3 S/m by adding the blending amounts of the CTAP from 0 to 50% mass ratio while simultaneously altering the equilibrium swelling ratio from 28.1 to 15.8. CHHs showed homogeneous porous structure, tunable swelling behavior, controllable conductivity, and good thermal stability. These results highlight that CHHs are attractive candidates to be used in biomedical applications., (Copyright © 2019 Elsevier B.V. All rights reserved.)

The chitosan/polyacrylic acid/polypyrrole/loaded with silver nanoparticles (CS/PAA/PPy/Ag-NPs) bionanocomposite as conductive, biodegradable, and biocompatible hydrogels were prepared by the casting method. Silver nanoparticles (Ag-NPs) were incorporated into the prepared bionanocomposite hydrogels to reinforce the electrical conductivity as well as the antimicrobial properties of the prepared hydrogels. The scanning electron microscopy revealed the compatibility of chitosan, polyacrylic acid, and polypyrrole, as well as Ag-NPs, were inserted in the polymer matrix and dispersed well on the superficies of the prepared bionanocomposites. X-ray diffraction displayed the presence of Ag-NPs into the polymer matrix. Also, the appearance of characteristic peaks in the Fourier transform infrared confirmed the compatibility of three polymers. Additionally, the swelling properties, antimicrobial activity as well as the electrical and dielectric characteristics of the fabricated bionanocomposites hydrogels were investigated. Moreover, the DC-conductivity was studied and our data designated that the DC-conductivity of the prepared bio-nanocomposites was improved by the existence of PPy more precisely than that of Ag-NPs. However, both were of high conductivity compared to that of the CS/PAA and found to follow the BNN universal relation. Also, The activation energy of about 55 kJ/mol of CS:2PAA hydrogel and reduce to about 15 kJ/mol in all the considered bionanocomposites after addition of Ag-NPs. Furthermore, the antibacterial activities of the knowledgeable microbes were improved as a result of the presence of Ag-NPs in bionanocomposites hydrogels., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Polyaniline (PANI) with/without polystyrene (PS), was successfully manufactured in the occurrence of dispersed pulp fibers via the oxidative polymerization reaction of aniline monomer to produce conductive paper sheets containing PANI, PANI/PS composites. Additionally, sliver nitrate (Ag-NO3) was added by varied loadings to the oxidative polymerization of aniline monomer to provide sliver nanoparticles (Ag-NPs) emptied into the prepared paper sheets. The prepared paper sheets were examined using scanning electron microscopy (SEM), X-ray diffraction (XRD) and infrared spectroscopy (IR), the mechanical properties of the prepared paper sheets were evaluated. Moreover, the electrical conductivity and biological studies such as cellulases assay, Microorganism & culture condition and detection of the released of Ag-NPs were evaluated. Furthermore, the prepared paper sheets were displayed good antibacterial properties contrary to gram positive and gram negative bacteria. Consequently, the prepared paper sheet may be used as novel materials for packaging applications., (Copyright © 2016 Elsevier Ltd. All rights reserved.)