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There is ongoing research for biomedical applications of polyvinyl alcohol (PVA)-based hydrogels; however, the execution of this has not yet been achieved at an appropriate level for commercialization. Advanced perception is necessary for the design and synthesis of suitable materials, such as PVA-based hydrogel for biomedical applications. Among polymers, PVA-based hydrogel has drawn great interest in biomedical applications owing to their attractive potential with characteristics such as good biocompatibility, great mechanical strength, and apposite water content. By designing the suitable synthesis approach and investigating the hydrogel structure, PVA-based hydrogels can attain superb cytocompatibility, flexibility, and antimicrobial activities, signifying that it is a good candidate for tissue engineering and regenerative medicine, drug delivery, wound dressing, contact lenses, and other fields. In this review, we highlight the current progresses on the synthesis of PVA-based hydrogels for biomedical applications explaining their diverse usage across a variety of areas. We explain numerous synthesis techniques and related phenomena for biomedical applications based on these materials. This review may stipulate a wide reference for future acumens of PVA-based hydrogel materials for their extensive applications in biomedical fields.

Polypyrrole (PPy)-based nanocomposite materials are of great interest to the scientific community owing to their usefulness in designing state-of-the-art industrial applications, such as fuel cells, catalysts and sensors, energy devices, and especially batteries. However, the commercialization of these materials has not yet reached a satisfactory level of implementation. More research is required for the design and synthesis of PPy-based composite materials for numerous types of battery applications. Due to the rising demand for environmentally friendly, cost-effective, and sustainable energy, battery applications are a significant solution to the energy crisis, utilizing suitable materials like PPy-based composites. Among the conducting polymers, PPy is considered an important class of materials owing to their ease of synthesis, low cost, environmentally friendly nature, and so on. In this context, PPy-based nanocomposites may be very promising due to their nanostructural properties and distinct morphological topography, which are vital concerns for their applications for battery applications. Such features of PPy-based nanocomposites make them particularly promising for next-generation electrode materials. However, the design and fabrication of appropriate PPy-based nanocomposites for battery applications is still a challenging area of research. This review paper describes the current progress on the synthesizing of PPy-based composites for battery applications along with their morphological topography. We discussed here the recent progress on the synthesis of different PPy-based composites, including PPy/S, PPy/MnOx, MWCNT/PPy, V2O5/PPy, Cl-doped PPy/rGO, and Fe/α-MnO2@PPy composites, by a polymerization approach for numerous battery applications. The insights presented in this review aim to provide a comprehensive reference for the future development of PPy-based composites in battery technology.

The achievement of large-scale applications of plasma-based polymers in biomedical sectors does not satisfy the appropriate level although a substantial amount of research is already performed. In this context, further investigations are necessary to design and synthesize plasma polymers for biomedical applications. Among the polymeric materials, plasma-based polymers have attracted substantial attention owing to their numerous advantages like faster processing, lower costs, eco-friendly waste, biocompatibility, and versatility, making them excellent materials for biomedical applications. Further, polymer synthesis using plasma polymerization techniques can avoid the time-consuming conventional multistep synthesis procedure. Plasma polymerization also offers a significant solution to overcome the numerous difficulties in the traditional approach where polymers can be directly attached to the desired surface using a plasma process, without disturbing the growing chain, and, thus, prevent an additional process such as grafting. Nevertheless, the design of appropriate plasma-based synthesis methods, optimization of the plasma process parameters, and exploration of polymer-based biocompatibility approaches are still challenging research areas. Regarding the surface morphological features of these plasma polymers, they possess several characteristics, such as wettability, adhesion capacity, and so on, that are important considerations in biomedical applications. In this review, numerous recent approaches to plasma polymerization methods along with different precursor phases used for such kind of synthesis of polymeric materials are discussed. The morphological aspect of the synthesized plasma polymers connected with biomedical applications is also reported in this review. Finally, promising aspects of plasma polymers for biomedical applications are briefly reported in this work. This review may offer an extensive reference for upcoming perceptions of plasma-based polymers and their applications in biomedical sectors.

Biodegradable polymers play an important role in environmental concerns compared to non-biodegradable polymers. Polyvinyl alcohol (PVA) is a biodegradable polymer with film-forming properties with antimicrobial and antioxidant activities and are considered for numerous practical applications in the industry, like food packaging, pharmaceuticals, and so on. The synthesis of PVA with promising properties like rheology, morphology, and mechanical performance is significant from the application point of view in industrial sectors. It is vital to realize the drawbacks and promising prospects associated with PVA rheology, morphology, and mechanical properties and how to address the problems concerning these properties. The present review describes the contemporary advancement of numerous synthesis approaches of PVA-based composite films and their rheology, morphology, and mechanical properties. This comprehensive review offers a comprehensive discussion of various strategies to enhance the rheology, morphology, and mechanical properties of composite films. It emphasizes modifications using environmentally friendly materials such as nanoparticles, metal oxides, polymers, and others. Additionally, existing challenges and the potential for forthcoming advancements in the properties of such composite films are discussed. The correlation between the PVA-based composite films and their promising properties like rheology, morphology, and mechanical performance may provide a reference for new insights into their applications in industrial sectors.

The current level of achievement in obtaining suitable polymer gel-based materials for efficient applications in thermoelectric devices is insufficient, although a substantial amount of research has already been performed. In this context, further investigations are necessary to design and synthesize polymer gel-based materials for ionic thermoelectric device applications. Polymer gel-based materials have attracted extensive consideration because of their multiple benefits, including easy processing, eco-friendly waste, and versatility, making them excellent materials for ionic thermoelectric devices. However, the design and synthesis of suitable polymer gel-based materials for ionic thermoelectric devices are still challenging areas of research. The surface morphological topography of prepared polymer gels is an important issue in thermoelectric device applications. In this review, significant approaches for the design and synthesis of polymer gel-based materials are discussed. This review may provide an important reference for upcoming perceptions on the design and synthesis of polymer gel materials for thermoelectric devices.

Poly(vinyl alcohol) (PVA)–ZnO–Al2O3 composite films have been prepared by the addition of different compositions of ZnO and Al2O3 through solvent casting method. Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–Vis) and photoluminescence spectroscopy (PL) spectra revealed the successful incorporation of ZnO and Al2O3 onto PVA and interactions among ZnO, Al2O3 and PVA molecules. PL data indeed showed the enhanced luminescence property of composite films compared with the PVA. Thermogravimetric analysis (TGA) data showed that thermal stability of PVA–ZnO–Al2O3 composite films could be greatly improved by the incorporation of ZnO and Al2O3 into the system. The glass transition temperature (Tg) were increased for the composite samples using ZnO and Al2O3. Differential scanning calorimetry (DSC) measurements revealed that the melting temperature (Tm) of PVA–ZnO–Al2O3 composite films are significantly higher (~ 12 to 25 °C) than PVA. The photocatalytic measurements exhibited better photocatalytic degradation ability of PVA–ZnO–Al2O3 composites over PVA. Such photocatalytic capacity makes the PVA–ZnO–Al2O3 composite films promising candidates for the removal of organic dyes for water purification.

Several kinds of acrylic-acid-grafted-starch (starch/AAc) hydrogels were prepared at room temperature (27°C) by applying 5, 10, 15, 20, and 25 kGy of gamma radiation to 15% AAc aqueous solutions containing 5, 7.5, and 15% of starch. With increment of the radiation dose, gel fraction became higher and attained the maximum (96.5%) at 15 kGy, above which the fraction got lowered. On the other hand, the gel fraction monotonically increased with the starch content. Swelling ratios were lower for the starch/AAc hydrogels prepared with higher gamma-ray doses and so with larger starch contents. Significant promotions of the swelling ratios were demonstrated by hydrolysis with NaOH: 13632±10% for 15 kGy radiation-dosed [5% starch/15% AAc] hydrogel, while the maximum swelling ratio was ~200% for those without the treatment. The authors further investigated the availability of the starch/AAc hydrogel as an adsorbent recovering dye waste from the industrial effluents by adopting methylene blue as a model material; the hydrogels showed high dye-capturing coefficients which increase with the starch ratio. The optimum dye adsorption was found to be 576 mg per g of the hydrogel having 7.5 starch and 15% AAc composition. Two kinetic models, (i) pseudo-first-order and (ii) pseudo-second-order kinetic models, were applied to test the experimental data. The latter provided the best correlation of the experimental data compared to the pseudo-first-order model.

Flexible sensors are revolutionizing wearable and implantable devices, with conductive hydrogels emerging as key materials due to their biomimetic structure, biocompatibility, tunable transparency, and stimuli-responsive electrical properties. However, their fragility and limited durability pose significant challenges for broader applications. Drawing inspiration from the self-healing capabilities of natural organisms like mussels, researchers are embedding self-repair mechanisms into hydrogels to improve their reliability and lifespan. This review highlights recent advances in self-healing (SH) conductive hydrogels, focusing on synthesis methods, healing mechanisms, and strategies to enhance multifunctionality. It also explores their wide-ranging applications, including in vivo signal monitoring, wearable biochemical sensors, supercapacitors, flexible displays, triboelectric nanogenerators, and implantable bioelectronics. While progress has been made, challenges remain in balancing self-healing efficiency, mechanical strength, and sensing performance. This review offers insights into overcoming these obstacles and discusses future research directions for advancing SH hydrogel-based bioelectronics, aiming to pave the way for durable, high-performance devices in next-generation wearable and implantable technologies.

This study aims to develop efficient and sustainable hydrogels for dye adsorption, addressing the critical need for improved wastewater treatment methods. Carboxymethyl cellulose (CMC)-based hydrogels grafted with AAc were synthesized using gamma radiation polymerization. Various AAc to CMC ratios (5:5, 5:7.5, 5:10, 5:15) were treated with 37% NaOH and exposed to 1–15 kGy radiation, with the optimal hydrogel obtained at 5 kGy. Swelling studies showed an increase in swelling with 5–7.5% AAc content, with the 5:7.5 hydrogel achieving the highest swelling at 18,774.60 (g/g). FTIR spectroscopy confirmed the interaction between AAc and CMC, indicating the successful formation of the hydrogel. DSC analysis revealed that higher AAc content led to increased glass transition and decomposition temperatures, thereby enhancing thermal stability. The swelling kinetics were linked to a reduction in pore size and improved AAc grafting. The 5:7.5 hydrogel demonstrated the highest adsorption capacity (681 mg/g) for methylene blue at 80 mg/L, achieving a desorption efficiency of 95% in 2M HCl. Kinetic analysis revealed non-uniform physisorption on a heterogeneous surface, which followed Schott’s pseudo-second-order model. This study advances the development of efficient hydrogels for water purification, providing a cost-effective and environmentally friendly solution for large-scale applications.

Hybrid supercapacitors (HSCs) have garnered growing interest for their ability to combine the high energy storage capability of batteries with the rapid charge–discharge characteristics of supercapacitors. This review examines the evolution of HSCs, emphasizing the synergistic mechanisms that integrate both Faradaic and non-Faradaic charge storage processes. Transition metal oxides (TMOs) are highlighted as promising battery-type electrodes owing to their notable energy storage potential and compatibility with various synthesis routes, including hydro/solvothermal methods, electrospinning, electrodeposition, and sol–gel processes. Particular attention is directed toward Ti-, Co-, and V-based TMOs, with a focus on tailoring their properties through morphology control, composite formation, and doping to enhance electrochemical performance. Overall, the discussion underscores the potential of HSCs to meet the growing demand for next-generation energy storage systems by bridging the gap between high energy and high power requirements.