Polymer Composite Hydrogel Based on Polyvinyl Alcohol/Polyacrylamide/Polybenzoxazine Carbon for Use in Flexible Supercapacitors.

Polymer gels are cross-linked polymer networks swollen by a solvent. These cross-linked networks are interconnected to produce a three-dimensional molecular framework. It is this cross-linked network that provides solidity to the gel and helps to hold the solvent in place. The present work deals with the fabrication of polybenzoxazine carbon (PBzC)-based gels that could function as a solid electrode in flexible supercapacitors (SCs). With the advantage of molecular design flexibility, polybenzoxazine-based carbon containing different hetero-atoms was synthesized. A preliminary analysis of PBzC including XRD, Raman, XPS, and SEM confirmed the presence of hetero-atoms with varying pore structures. These PBz-carbons, upon reaction with polyvinyl alcohol (PVA) and acrylamide (AAm), produced a composite polymer hydrogel, PVA/poly (AAm)/PBzC. The performance of the synthesized hydrogel was analyzed using a three-electrode system. PVA/poly (AAm)/PBzC represented the working electrode. The inclusion of PBzC within the PVA/poly (AAm) matrix was evaluated by cyclic voltammetry and galvanostatic charge/discharge measurements. A substantial increase in the CV area and a longer charge/discharge time signified the importance of PBzC inclusion. The PVA/poly (AAm)/PBzC electrode exhibited larger specific capacitance (Cs) of 210 F g-1 at a current density of 0.5 A g-1 when compared with the PVA/poly (AAm) electrode [Cs = 92 F g-1]. These improvements suggest that the synthesized composite hydrogel can be used in flexible supercapacitors requiring light weight and wearability.

Flexible Composite Hydrogels Based on Polybenzoxazine for Supercapacitor Applications.

Polybenzoxazines (Pbzs) are advanced forms of phenolic resins that possess many attractive properties, including thermal-induced self-curing polymerization, void-free polymeric products and absence of by-product formation. They also possess high Tg (glass transition temperature) and thermal stability. But the produced materials are brittle in nature. In this paper, we present our attempt to decrease the brittleness of Pbz by blending it with polyvinylalcohol (PVA). Benzoxazine monomer (Eu-Ed-Bzo) was synthesized by following a simple Mannich condensation reaction. The formation of a benzoxazine ring was confirmed by FT-IR and NMR spectroscopic analyses. The synthesized benzoxazine monomer was blended with PVA in order to produce composite films, PVA/Pbz, by varying the amount of benzoxazine monomer (1, 3 and 5 wt. % of PVA). The property of the composite films was studied using various characterization techniques, including DSC, TGA, water contact angle analysis (WCA) and SEM. WCA analysis proved that the hydrophobic nature of Pbz (value) was transformed to hydrophilic (WCA of PVA/Pbz5 is 35.5°). These composite films could play the same role as flexible electrolytes in supercapacitor applications. For this purpose, the composite films were immersed in a 1 M KOH solution for 12 h in order to analyze their swelling properties. Moreover, by using this swelled gel, a symmetric supercapacitor, AC//PVA/Pbz5//AC, was constructed, exhibiting a specific capacitance of 170 F g-1.

Innovative Carbon Ball Frameworks: Elevating Energy Storage Performance and Enhancing CO2 Capture Efficiency.

A novel porous carbon, derived from polybenzoxazine and subjected to hydrogen peroxide treatment, has been meticulously crafted to serve dual functions as a supercapacitor and a CO2 capture material. While supercapacitors offer a promising avenue for electrochemical energy storage, their widespread application is hampered by relatively low energy density. Addressing this limitation, our innovative approach introduces a three-dimensional holey carbon ball framework boasting a hierarchical porous structure, thereby elevating its performance as a metal-free supercapacitor electrode. The key to its superior performance lies in the intricate design, featuring a substantial ion-accessible surface area, well-established electron and ion transport pathways, and a remarkable packing density. This unique configuration endows the holey carbon ball framework electrode with an impressive capacitance of 274 F g-1. Notably, the electrode exhibits outstanding rate capability and remarkable longevity, maintaining a capacitance retention of 82% even after undergoing 5000 cycles in an aqueous electrolyte. Beyond its prowess as a supercapacitor, the hydrogen peroxide-treated porous carbon component reveals an additional facet, showcasing an exceptional CO2 adsorption capacity. At temperatures of 0 and 25 °C, the carbon material displays a CO2 adsorption capacity of 4.4 and 4.2 mmol/g, respectively, corresponding to equilibrium pressures of 1 bar. This dual functionality renders the porous carbon material a versatile and efficient candidate for addressing the energy storage and environmental challenges of our time.

Polybenzoxazine-Based Nitrogen-Containing Porous Carbon and Their Composites with NiCo Bimetallic Oxides for Supercapacitor Applications.

Supercapacitors (SCs) are considered as emerging energy storage devices that bridge the gap between electrolytic capacitors and rechargeable batteries. However, due to their low energy density, their real-time usage is restricted. Hence, to enhance the energy density of SCs, we prepared hetero-atom-doped carbon along with bimetallic oxides at different calcination temperatures, viz., HC/NiCo@600, HC/NiCo@700, HC/NiCo@800 and HC/NiCo@900. The material produced at 800 °C (HC/NiCo@800) exhibits a hierarchical 3D flower-like morphology. The electrochemical measurement of the prepared materials was performed in a three-electrode system showing an enhanced specific capacitance for HC/NiCo@600 (Cs = 1515 F g-1) in 1 M KOH, at a current density of 1 A g-1, among others. An asymmetric SC device was also fabricated using HC/NiCo@800 as anode and HC as cathode (HC/NiCo@600//HC). The fabricated device had the ability to operate at a high voltage window (~1.6 V), exhibiting a specific capacitance of 142 F g-1 at a current density of 1 A g-1; power density of 743.11 W kg-1 and energy density of 49.93 Wh kg-1. Altogether, a simple strategy of hetero-atom doping and bimetallic inclusion into the carbon framework enhances the energy density of SCs.

Rapid Transformation in Wetting Properties of PTFE Membrane Using Plasma Treatment.

In this paper, we describe the surface modification of polytetrafluoroethylene (PTFE) through the plasma treatment process. Several parameters including different active gases, RF power, distance between the plasma source and sample, and plasma duration were optimized to reduce the hydrophobic nature of PTFE. Three different active gases were used (i.e., N2, O2, and (Ar+H2)); N2 was effective to reduce the hydrophobicity of PTFE within a shorter plasma duration of 2 min. Several surface characterizations including ATR-FTIR, water contact angle, FE-SEM, and XPS were utilized to verify the neat and modified PTFE surface after plasma treatment. The plasma treatment using N2 as an active gas improved the wettability of the PTFE membrane, showing a water contact angle of 109.5° when compared with the neat PTFE (141.9°). The SEM images of plasma-treated PTFE showed greater modifications on the surface indicating non-uniform fiber alignment and torn fibers at several places. The obtained results confirm the fact that plasma treatment is an effective way to modify the PTFE surface without altering its bulk property.

Enhanced Activity and Stability of Heteroatom-Doped Carbon/Bimetal Oxide for Efficient Water-Splitting Reaction.

The research community is actively exploring ways to create cost-efficient and high-performing electrocatalysts for the oxygen evolution reaction. In this investigation, an innovative technique was employed to produce heteroatom-doped carbon containing NiCo oxides, i.e., HC/NiCo oxide@800, in the form of a three-dimensional hierarchical flower. This method involved the reduction of a bimetallic (Ni, Co) metal-organic framework, followed by carefully controlled oxidative calcination. The resulting porous flower-like structure possess numerous advantages, such as expansive specific surface areas, excellent conductivity, and multiple electrocatalytic active sites for both hydrogen and oxygen evolution reactions. Moreover, the presence of oxygen vacancies within HC/NiCo oxide@800 significantly enhances the conductivity of the NiCo substance, thus expediting the kinetics of both the processes. These benefits work together synergistically to enhance the electrocatalytic performance of HC/NiCo oxide@800. Empirical findings reveal that HC/NiCo oxide@800 electrocatalysts demonstrate exceptional catalytic activity, minimal overpotential, and remarkable stability when deployed for both hydrogen evolution and oxygen evolution reactions in alkaline environments. This investigation introduces a fresh avenue for creating porous composite electrocatalysts by transforming metal-organic frameworks with controllable structures. This approach holds promise for advancing electrochemical energy conversion devices by facilitating the development of efficient and customizable electrocatalytic materials.

Facile Synthesis of Nitrogen-Rich Porous Carbon/NiMn Hybrids Using Efficient Water-Splitting Reaction.

Proper design of multifunctional electrocatalyst that are abundantly available on earth, cost-effective and possess excellent activity and electrochemical stability towards oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are required for effective hydrogen generation from water-splitting reaction. In this context, the work herein reports the fabrication of nitrogen-rich porous carbon (NRPC) along with the inclusion of non-noble metal-based catalyst, adopting a simple and scalable methodology. NRPC containing nitrogen and oxygen atoms were synthesized from polybenzoxazine (Pbz) source, and non-noble metal(s) are inserted into the porous carbon surface using hydrothermal process. The structure formation and electrocatalytic activity of neat NRPC and monometallic and bimetallic inclusions (NRPC/Mn, NRPC/Ni and NRPC/NiMn) were analyzed using XRD, Raman, XPS, BET, SEM, TEM and electrochemical measurements. The formation of hierarchical 3D flower-like morphology for NRPC/NiMn was observed in SEM and TEM analyses. Especially, NRPC/NiMn proves to be an efficient electrocatalyst providing an overpotential of 370 mV towards OER and an overpotential of 136 mV towards HER. Moreover, it also shows a lowest Tafel slope of 64 mV dec-1 and exhibits excellent electrochemical stability up to 20 h. The synergistic effect produced by NRPC and bimetallic compounds increases the number of active sites at the electrode/electrolyte interface and thus speeds up the OER process.

Heteroatom-Enhanced Porous Carbon Materials Based on Polybenzoxazine for Supercapacitor Electrodes and CO2 Capture.

Through a solution method utilizing benzoxazine chemistry, heteroatoms containing porous carbons (HCPCs) were synthesized from melamine, eugenol and formaldehyde, followed by carbonization in a nitrogen atmosphere and chemical activation with KOH at three different activation temperatures, 700, 800 and 900 °C. The introduction of melamine and eugenol to the monomer produced structurally bonded nitrogen and oxygen in porous carbons. Changing the calcination temperature can alter the doping level of heteroatoms and the particle size. These carbon materials exhibit large pore size distributions, tunable pore structure, high nitrogen and oxygen contents and high surface areas, which make them suitable for use as electrode materials in supercapacitors. As a result of activating at 800 °C, the sample HCPC-800 exhibits a high specific surface area of 984 m2/g, high oxygen and nitrogen content (3.64-6.26 wt.% and 10.61-13.65 wt.%), hierarchical pore structure, high degree of graphitization and good electrical conductivity. An outstanding rate capability is also demonstrated, as well as incredible longevity, retaining the capacitance up to 83% even after 5000 cycles in a solution containing 1 M H2SO4. Moreover, the activated porous carbon containing nitrogen exhibits a CO2 adsorption capacity of 3.6 and 3.5 mmol/g at 25 °C and 0 °C, respectively, which corresponds to equilibrium pressures of 1 bar.

Synthesis of Bio-Based Polybenzoxazine and Its Antibiofilm and Anticorrosive Activities.

Candida albicans are highly widespread pathogenic fungi in humans. Moreover, its developed biofilm causes serious clinical problems, leading to drug failure caused by its inherent drug tolerance. Hence, the inhibition of biofilm formation and virulence characteristics provide other means of addressing infections. Polymer composites (PCs) derived from natural products have attracted increasing interest in the scientific community, including antimicrobial applications. PCs are a good alternative approach to solving this challenge because of their excellent penetration power inside biofilms. The main objectives of this study were to synthesize a novel curcumin-based polybenzoxazine polymer composite (poly(Cu-A) PC) using Mannich condensation reaction and evaluate their potency as an antibiofilm and anticorrosive candidate against C. albicans. In addition, their anticorrosive efficacy was also explored. PC exhibited significant antibiofilm efficacy versus C. albicans DAY185 by the morphologic changing of yeast to hyphae, and>90% anticorrosive efficacy was observed at a higher dose of PC. These prepared PC were safe in vivo against Caenorhabditis elegans and Raphanus raphanistrum. The study shows that a polybenzoxazine polymer composite has the potential for controlling biofilm-associated fungal infections and virulence by C. albicans, and opens a new avenue for designing PCs as antifungal, anticorrosive agents for biofilm-associated fungal infections and industrial remediation.

Bio-Based Polybenzoxazine-Cellulose Grafted Films: Material Fabrication and Properties.

Despite the fact that amino cellulose (AC) is biodegradable, biocompatible, and has excellent film-forming properties, AC films have poor mechanical properties and are not thermally stable. An AC-based composite film prepared from AC and curcumin-stearylamine based benzoxazine (C-st) is reported in order to improve its performance and promote its application. As starting materials, C-st and AC were used to produce a C-st/AC composite film possessing a synergistic property through chemical cross-linking and hydrogen bonds. Two salient features with respect to the curing behavior were obtained. Firstly, the onset of curing was reduced to 163 °C when the benzoxazine monomer was synthesized from fully bio-based precursors (such as curcumin and stearylamine). Secondly, a synergistic effect in curing behavior was obtained by mixing C-st with AC. As a result of tensile tests and thermal analysis, the poly(C-st) benefited the composite films with pronounced mechanical and thermal properties, even at elevated temperatures. There was a 2.5-fold increase in tensile strength compared to the AC film, indicating that the composite films have the potential to be used for functional purposes. These poly(C-st)/AC films with improved mechanical and thermal properties have the ability to replace naturally occurring polymer films in film-related applications.

Sustainable Chitosan/Polybenzoxazine Films: Synergistically Improved Thermal, Mechanical, and Antimicrobial Properties.

Polybenzoxazines (Pbzs) are considered as an advanced class of thermosetting phenolic resins as they overcome the shortcomings associated with novolac and resole type phenolic resins. Several advantages of these materials include curing without the use of catalysts, release of non-toxic by-products during curing, molecular design flexibility, near-zero shrinkage of the cured materials, low water absorption and so on. In spite of all these advantages, the brittleness of Pbz is a knotty problem that could be solved by blending with other polymers. Chitosan (Ch), has been extensively investigated in this context, but its thermal and mechanical properties rule out its practical applications. The purpose of this work is to fabricate an entirely bio-based Pbz films by blending chitosan with benzoxazine (Bzo), which is synthesized from curcumin and furfuryl amine (curcumin-furfurylamine-based Bzo, C-fu), by making use of a benign Schiff base chemistry. FT-IR and 1H-NMR spectroscopy were used to confirm the structure of C-fu. The impact of chitosan on benzoxazine polymerization was examined using FT-IR and DSC analyses. Further evidence for synergistic interactions was provided by DSC, SEM, TGA, and tensile testing. By incorporating C-fu into Ch, Ch-grafted-poly(C-fu) films were obtained with enhanced chemical resistance and tensile strength. The bio-based polymer films produced inhibited the growth of Staphylococcus aureus and Escherichia coli, by reversible labile linkages, expanding Ch galleries, and releasing phenolic species, which was 125 times stronger than bare Ch. In addition, synthesized polybenzoxazine films [Ch/Poly(C-fu)] showed significant dose-dependent antibiofilm activity against S. aureus and E. coli as determined by confirmed by confocal laser scanning microscopy (CLSM). This study suggests that bio-based Ch-graft-polymer material provide improved anti-bacterial property and characteristics that may be considered as a possibility in the near future for wound healing and implant applications.

Thermoplastic Starch Composites Reinforced with Functionalized POSS: Fabrication, Characterization, and Evolution of Mechanical, Thermal and Biological Activities.

Rapid advancements in materials that offer the appropriate mechanical strength, barrier, and antimicrobial activity for food packaging are still confronted with significant challenges. In this study, a modest, environmentally friendly method was used to synthesize functionalized octakis(3-chloropropyl)octasilsesquioxane [fn-POSS] nanofiller. Composite films compared to the neat thermoplastic starch (TS) film, show improved thermal and mechanical properties. Tensile strength results improved from 7.8 MPa to 28.1 MPa (TS + 5.0 wt.% fn-POSS) with fn-POSS loading (neat TS). The barrier characteristics of TS/fn-POSS composites were increased by fn-POSS by offering penetrant molecules with a twisting pathway. Also, the rates of O2 and H2O transmission were decreased by 50.0 cc/m2/day and 48.1 g/m2/day in TS/fn-POSS composites. Based on an examination of its antimicrobial activity, the fn-POSS blended TS (TSP-5.0) film exhibits a favorable zone of inhibition against the bacterial pathogenic Staphylococcus aureus and Escherichia coli. The TS/fn-POSS (TSP-5.0) film lost 78.4% of its weight after 28 days in natural soil. New plastic materials used for packaging, especially food packaging, are typically not biodegradable, so the TS composite with 5.0 wt.% fn-POSS is therefore of definite interest. The incorporation of fn-POSS with TS composites can improve their characteristics, boost the use of nanoparticles in food packaging, and promote studies on biodegradable composites.