Jinlong Zuo

In this study, pomelo peel waste was utilized as the raw material to extract flavonoids, which were subsequently microencapsulated with β-cyclodextrin (β-CD) and incorporated into a corn starch/konjac glucomannan composite film matrix, aiming to develop biodegradable candidate films containing an antioxidant extract for potential food packaging applications. The extraction conditions for pomelo peel flavonoids (PF) were optimized via response surface methodology, yielding the optimal parameters as follows: extraction time of 123.88 min, temperature of 69.07 °C, etc., under which the total PF extraction rate reached 5.958%. At high concentrations, the 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging capacities of the obtained PF did not differ significantly from those of ascorbic acid. The fabricated PF-loaded β-cyclodextrin microcapsules (PF-CD-MCs) achieved an encapsulation efficiency of 71.24 ± 0.21%, the morphological and spectroscopic results suggested the successful formation of the inclusion complex and were incorporated into the composite films at varying addition levels ranging from 0% to 40% (w/w). The results demonstrated that the loading content of PF-CD-MCs played a critical regulatory role in the microstructure and macroscopic properties of the films. At 10% loading, the water vapor permeability (WVP) reached its minimum, whereas 20% loading provided the best overall compromise: the microcapsules remained uniformly dispersed without recrystallization, the film retained acceptable barrier and mechanical performance, and the active loading was higher than that at 10%. At 30%–40%, aggregation and recrystallization caused structural defects and marked deterioration in WVP, mechanical strength, and water resistance. Therefore, 20% is recommended as a comprehensive loading level rather than a single-property optimum. This study provides important theoretical foundations and technical references for the high-value utilization of pomelo peel waste and the rational design of biodegradable active packaging materials.

In this study, a carbon felt (CF)-based ternary composite anode was developed through the decoration of nickel cobaltite (NiCo₂O₄) nano-needles and subsequent in situ electropolymerization of polypyrrole (PPy). The structural and electrochemical properties of the modified electrodes were systematically characterized. The CF/NiCo₂O₄/PPy anode demonstrated significantly enhanced bioelectrochemical activity, achieving a peak current density of 96.0 A/m² and a steady-state current density of 28.9 A/m², which were 4.85 and 5.90 times higher than those of bare carbon felt, respectively. Geobacteriaceae is a type of electrogenic bacteria. It was hardly detected on the bare CF substrate; however, in the ternary CF/NiCo2O4/PPy electrode, the relative abundance of Geobacteriaceae significantly increased to 43%. Moreover, the composite electrode exhibited superior charge storage performance, with a total charge (Q_t) of 32,509.0 C/m² and a stored charge (Q_s) of 3609.0 C/m² measured under a 1000 s charging/discharging period. The MFC configured with the CF/NiCo₂O₄/PPy anode reached a maximum power density of 1901.25 mW/m² at an external resistance of 200 Ω, nearly six times that of the unmodified CF-based MFC. These improvements are attributed to the synergistic interaction between the pseudocapacitive NiCo₂O₄ and conductive PPy, which collectively facilitate electron transfer, promote microbial colonization, and enhance interfacial redox kinetics. This work provides an effective strategy for designing high-performance MFC electrodes with dual functionality in energy storage and power delivery.

This study addresses the challenge of chitosan (CS) being difficult to dissolve in water due to its highly ordered crystalline structure. Chitosan is modified with chloroacetic acid to reduce its crystallinity and enhance its water solubility. Through single-factor experiments, the optimal conditions for preparing carboxymethyl chitosan film (CMCS) were determined: under conditions of 50 °C, a cellulose substrate (CS) concentration of 18.75 g/L, a NaOH concentration of 112.5 g/L, and a chloroacetic acid concentration of 18.75 g/L, the reaction proceeded for 5 h. Under these conditions, the resulting carboxymethyl chitosan film exhibited the best flocculation effect, forming chitosan films in water that had flocculation activity toward mung bean starch protein wastewater. The successful introduction of carboxyl groups at the N and O positions of the chitosan molecular chain, which reduced the crystallinity of chitosan and enhanced its water solubility, was confirmed through analysis using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The prepared carboxymethyl chitosan film (CMCS) was applied in the flocculation recovery of protein. Through single-factor and response surface experiments, the optimal process conditions for flocculating and recovering protein with CMCS were determined: a CMCS dosage of 1.1 g/L, a reaction time of 39.6 min, a reaction temperature of 42.7 °C, and a pH of 5.2. Under these conditions, the protein recovery rate reached 56.97%. The composition and amino acid profile of the flocculated product were analyzed, revealing that the mung bean protein flocculated product contained 62.33% crude protein. The total essential amino acids (EAAs) accounted for 52.91%, non-essential amino acids (NEAAs) for 47.09%, hydrophobic amino acids for 39.56%, and hydrophilic amino acids for 12.67%. The ratio of aromatic to branched-chain amino acids was 0.31, and the ratio of basic to acidic amino acids was 1.68. These findings indicate that the recovered product has high surface activity and good protein stability, foaming ability, and emulsifying properties.

Microbial Fuel Cell (MFC) is a novel bioelectrochemical system that catalyzes the oxidation of chemical energy in organic waste and converts it directly into electrical energy through the attachment and growth of electroactive microorganisms on the electrode surface. This technology realizes the synergistic effect of waste treatment and renewable energy production. A CF-NiO-PANI capacitor composite anode was prepared by loading polyaniline on a CF-NiO electrode to improve the capacitance of a CF electrode. The electrochemical characteristics of the composite anode were evaluated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), and the electrode materials were analyzed comprehensively by scanning electron microscopy (SEM), energy diffusion spectrometer (EDS), and Fourier transform infrared spectroscopy (FTIR). MFC system based on CF-NiO-PANI composite anode showed excellent energy conversion efficiency in potato starch wastewater treatment, and its maximum power density increased to 0.4 W/m³, which was 300% higher than that of the traditional CF anode. In the standard charge–discharge test (C1000/D1000), the charge storage capacity of the composite anode reached 2607.06 C/m², which was higher than that of the CF anode (348.77 C/m²). Microbial community analysis revealed that the CF-NiO-PANI anode surface formed a highly efficient electroactive biofilm dominated by electrogenic bacteria (accounting for 47.01%), confirming its excellent electron transfer ability. The development of this innovative capacitance-catalytic dual-function anode material provides a new technical path for the synergistic optimization of wastewater treatment and energy recovery in MFC systems.

Microbial fuel cells (MFCs) generate electricity through the microbial oxidation of organic waste. However, the inherent electrochemical performance of carbon felt (CF) electrodes is relatively poor and requires enhancement. In this study, nickel oxide (NiO) was successfully loaded onto CF to improve its electrode performance, thereby enhancing the electricity generation capacity of MFCs during the degradation of treated wastewater. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and energy diffusion spectrometer (EDS) analyses confirmed the successful deposition of NiO on the CF surface. The modification enhanced both the conductivity and capacitance of the electrode and increased the number of microbial attachment sites on the carbon fiber filaments. The prepared CF–NiO electrode was employed as the anode in an MFC, and its electrochemical and energy storage performance were evaluated. The maximum power density of the MFC with the CF–NiO anode reached 0.22 W/m², compared to 0.08 W/m² for the unmodified CF anode. Under the C1000-D1000 condition, the charge storage capacity and total charge output of the CF–NiO anode were 1290.03 C/m² and 14,150.03 C/m², respectively, which are significantly higher than the 452.9 C/m² and 6742.67 C/m² observed for the CF anode. These results indicate notable improvements in both power generation and energy storage performance. High-throughput gene sequencing of the anodic biofilm following MFC acclimation revealed that the CF–NiO anode surface hosted a higher proportion of electroactive bacteria. This suggests that the NiO modification enhances the biodegradation of organic matter and improves electricity generation efficiency.

Microbial fuel cells (MFCs) are a novel bioenergy technology that utilizes microorganisms to catalyze the conversion of fuels into electricity. However, traditional MFCs are constrained by the low electricity generation capacity of microorganisms, resulting in relatively low power output. Additionally, the inability of traditional MFCs to store electricity significantly limits their practical applications. In this study, we fabricate a novel oxide graphite/nickel cobalt oxide (GO/NiCo₂O₄) capacitive composite bioanode material supported on stainless-steel fiber felt (SSFF). This composite material combines the excellent biocompatibility of graphite oxide and the energy storage capacity of nickel cobalt oxide. Consequently, the prepared anode exhibits significant advantages, including high specific capacitance, efficient electron transport, and enhanced biocompatibility. The MFC with the SSFF/GO/NiCo₂O₄ anode demonstrated a significantly enhanced power density, achieving a maximum of 1267.5 mW/m²—1.38-fold and 2.23-fold higher than those of the SSFF/GO and SSFF anodes, respectively. Moreover, the modified anode (SSFF/GO/NiCo₂O₄) exhibited a stored charge (Q_s) of 1405.35 C/m², representing 2.61-fold and 35.79-fold increases compared to the SSFF/GO and SSFF anodes, respectively. High-throughput analysis revealed that SSFF/GO/NiCo₂O₄-modified anode achieved an electrogenic bacterial efficiency exceeding 81%, which was significantly higher than that of the SSFF/GO and SSFF anodes. The results of this study not only provide valuable insights and theoretical guidance for the development of MFCs using capacitive composite anode materials, they also present sustainable power solutions for low-power electronic systems, such as miniaturized sensors and IoT devices.

With the advancement of China’s agricultural modernization and scientific and technological progress, there has been a substantial increase in corn production, resulting in significant agricultural waste of materials such as corncobs. Conventional incineration methods fail to efficiently utilize the recyclable resources present in corncobs. In this investigation, corncob biochar film (CBC) was synthesized through the pyrolysis of corncob. Single-factor and orthogonal experiments were used to determine the conditions needed to prepare biochar film with the best Cr(VI) adsorption effect. The experiments showed that at a heating rate of 5 °C/min, pyrolysis temperature of 500 °C and pyrolysis time of 120 min, the Cr(VI) removal rate of prepared biochar film reached 73.55% and the adsorption capacity was 18.39 mg/g. Meanwhile, the factors affecting the removal of Cr(VI), including pH value, initial concentration of Cr(VI) solution, dosage of adsorbent, adsorption kinetics and isothermal adsorption, were analyzed in detail. The structures of CBC before and after Cr(VI) adsorption were analyzed by SEM, FTIR, XRD, XPS, and BET. These findings demonstrate the efficacy of corncob biochar film in Cr(VI) removal.

Biochar, a carbon-dense material known for its substantial specific surface area, remarkable porosity, diversity of functional groups, and cost-effective production, has garnered widespread acclaim as a premier adsorbent for the elimination of heavy metal ions and organic contaminants. Nevertheless, the application of powdered biochar is hindered by the challenges associated with its separation from aqueous solutions, and without appropriate management, it risks becoming hazardous waste. To facilitate its use as an immobilization medium, biochar necessitates modification. In this investigation, sodium alginate, celebrated for its superior gelation capabilities, was amalgamated with polyvinyl alcohol to bolster mechanical robustness, thereby embedding biochar to formulate sodium alginate biochar microspheres (PVA/SA-FMB). A meticulously designed response surface methodology experiment was employed to ascertain the optimal synthesis conditions for PVA/SA-FMB. Characterization outcomes unveiled a highly developed surface abundant in functional groups and confirmed the successful incorporation of iron ions. Adsorption trials revealed that at a temperature of 25 °C and a pH of 2, the adsorption capacity of PVA/SA-FMB for Cr(VI) was 13.7 mg/g within the initial 30 min, reaching an equilibrium capacity of 26.03 mg/g after 1440 min. Notably, the material sustained a Cr(VI) removal efficiency exceeding 90% across five cycles, underscoring its rapid and effective Cr(VI) eradication performance. Kinetic and isothermal adsorption analyses suggested that the adsorption of Cr(VI) adheres to a pseudo-second-order kinetic model and the Freundlich isotherm, indicative of monolayer adsorption dominated by reaction mechanisms. X-ray photoelectron spectroscopy (XPS) analysis inferred that the adsorption mechanism predominantly encompasses electrostatic attraction, redox processes, and complex formation.

This study focuses on synthesizing a composite material of Ag/ZnO/BiOCl using Ag, ZnO, and BiOCl as raw materials. The material was prepared by loading Ag and BiOCl onto ZnO nanofilms, aiming to enhance the photocatalytic degradation of ciprofloxacin (CIP). Optimization of the photocatalytic degradation process through single-factor experiments revealed that under conditions of an initial CIP pH of 9, an Ag/ZnO/BiOCl dosage of 1 g/L, and an initial CIP concentration of 5 mg/L the conversion efficiency of CIP reached 98.79% after 150 min of exposure to a 250 W xenon lamp simulating sunlight. Furthermore, the composite material maintained a conversion efficiency of 86.17% for CIP even after five cycles of reuse, demonstrating its excellent stability. The optical properties, elemental composition, valence state, crystallinity, and morphology of the samples were analyzed using techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL), UV–visible diffuse reflectance spectroscopy (UV-vis DRS), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The results indicate that the introduction of Ag expanded the light response range of ZnO, while the addition of BiOCl improved the separation efficiency of electron–hole pairs in the composite nanomaterial. The photocatalytic mechanism was further elucidated through radical scavenging experiments, confirming that ·OH and h⁺ are the main active species in the degradation process.