Integrated tea polyphenols and polydopamine functionalized graphene anode for improved bioelectricity generation and Cr(VI) reduction in microbial fuel cells.

Microbial fuel cells (MFCs) have the dual advantage of mitigating Cr(Ⅵ) wastewater ecological threats while generating electricity. However, the low electron transfer efficiency and the limited enrichment of active electrogens are barriers to MFCs advancement. This study describes the synthesis of the TP-PDA-RGO@CC negative electrode using tea polyphenol as a reducing agent and polydopamine-doped graphene, significantly enhances the roughness and hydrophilicity of the anode. The charge transfer resistance was reduced by 94%, and the peak MFC power was 1375.80 mW·m-2. Under acidic conditions, the Cr(Ⅵ) reduction rate reached 92% within 24 h, with a 52% increase in coulombic efficiency. Biodiversity analysis shows that the TP-PDA-RGO@CC anode could enrich electrogens, thereby boosting the electron generation mechanism at the anode and enhancing the reduction efficiency of Cr(Ⅵ) in the cathode chamber. This work emphasizes high-performance anode materials for efficient pollutant removal, energy conversion, and biomass reuse.

Natural tea polyphenol functionalized graphene anode for simultaneous power production and degradation of methyl orange dye in microbial fuel cells.

The microbial fuel cell (MFCs) has dual functions, capable of achieving dye decolorization and synchronous power generation. Despite these advantages, the MFCs have faced challenges related to low electron transfer efficiencies and limited dye treatment capacity in wastewater applications. This work introduces an innovative approach by employing reduced graphene oxide-modified carbon cloth (TP-RGO@CC) anodes, utilizing tea polyphenols as the reducing agent. This modification significantly enhances the hydrophilicity and biocompatibility of the anodes. The MFC equipped with the TP-RGO@CC anode demonstrated a remarkable increase in the maximum power density, reaching 773.9 mW m-2, representing a 22% improvement over the plain carbon cloth electrode. The decolorization rate of methyl orange (50 mg L-1, pH 7) reached 99% within 48 h. Biodiversity analysis revealed that the TP-RGO@CC anode selectively enriched electrogens producing and organic matter-degrading bacteria, promoting a dual mechanism of dye decolorization, degradation, and simultaneous electro-production at the anode. This work highlights advanced anode materials that excel in effective pollutant removal, energy conversion, and biomass reuse.

MgO-modified biochar by modifying hydroxyl and amino groups for selective phosphate removal: Insight into phosphate selectivity adsorption mechanism through experimental and theoretical.

Metal oxides-modified biochars have been widely studied as promising adsorbents for removing phosphate from wastewater discharge. Yet, the low adsorption selectivity towards phosphate severely limits its potential in practical applications. In this study, MgO-modified biochar modified by hydroxyl and amino groups (OH/NH2@MBC) is developed for selective phosphorus recovery from wastewater. As major results, the OH/NH2@MBC exhibits favorable phosphate adsorption performance is superior to that of MBC resin in the presence of co-existing anions (NO3-, Cl-, HCO3- and SO42-) and natural organic matter (humic acid) even actual wastewater, suggesting its superior selectivity towards phosphate. The OH/NH2@MBC shows an excellent phosphate adsorption capacity (43.27 mg/g) and desorption ratio (82.34 %) after five cycles under the condition of anion coexistence (100 mg/L). The experimental and DFT theoretical study reveals that attaching hydroxyl and amino groups onto the MBC surface, which facilitates to inhibiting the side effects of anions (NO3-, Cl-, HCO3-, and SO42-) through Lewis acid-base sites, hydrogen bonds, and metal affinity, and preferentially select adsorption P, contributing greatly to improve phosphate adsorption selectivity. Importantly, the presence of amino and hydroxyl groups can reduce the Fermi level of OH/NH2@MgO(220) and OH/NH2@MgO(200) and improve the adsorption selection for HPO42-. This study provides an effective strategy for enhancing the adsorption selectivity of metal oxides-modified biochars towards phosphate through modifying functional groups.

Bi-functional biochar-g-C3N4-MgO composites for simultaneously minimizing pollution：Photocatalytic degradation of pesticide and phosphorus recovery as slow-release fertilizer.

Significant progress has been made in the development of phosphorus recovery adsorbents and photocatalysts for degradation of pesticides. However, the bifunctional materials for phosphorus recovery and photocatalytic degradation of pesticides have not been designed, and the mechanism of the interaction between photocatalysis and P adsorption remains unexplored. Herein, we develop biochar-g-C3N4-MgO composites (BC-g-C3N4-MgO) with bi-function application to minimize water toxicity and eutrophication. The results show phosphorus adsorption capacity of the BC-g-C3N4-MgO composite reaches 111.0 mg·g-1, and its degradation ratio of dinotefuran reaches 80.1% within 260 min. The mechanism studies show that MgO can play variety roles in BC-g-C3N4-MgO composite, in which can improve the adsorption capacity of phosphorus, enhance the utilization efficiency of visible light and the separation efficiency of photoinduced electron-hole pairs. The biochar existed in BC-g-C3N4-MgO serves as charge transporter with a good conductivity, which promotes the fluent transfer of photo-generated charge carriers. The ESR indicates that both •O2- and •OH generated from BC-g-C3N4-MgO are responsible for dinotefuran degradation. Finally, pot experiments reveal that P laden BC-g-C3N4-MgO promotes the growth of pepper seedlings with high P utilization efficiency of 49.27%.

Core-shell P-laden biochar/ZnO/g-C3N4 composite for enhanced photocatalytic degradation of atrazine and improved P slow-release performance.

Technologies that can effectively address the environmental issues arisen from the use of agrochemicals and P fertilizers are needed for the development of green agriculture. Here, we reporta new core-shell P-laden biochar/ZnO/g-C3N4 composite (Pbi-ZnO-g-C3N4) used both as an efficient photocatalyst for degrading atrazine and a promising slow-release fertilizer for improving the P utilization efficiency. In comparison with P-laden biochar/ZnO (Pbi-ZnO), Pbi-ZnO-g-C3N4 exhibits enhanced photocatalytic activity with the maximum atrazine degradation efficiency of 85.3% after 260 min. Pbi-ZnO-g-C3N4 also shows superior P slow-release performance with the cumulative P release concentration of 216.40 g/L in 260 min. Besides, it is found that the coating of g-C3N4 on the surface of Pbi-ZnO improves the utilization of visible light and separation of photoinduced electron-hole pairs, producing more radicals (•OH and •O2-) under visible light irradiation. The mechanistic study reveals that Z-shaped heterojunction is formed between ZnO and g-C3N4 in Pbi-ZnO-g-C3N4, and biochar serves as an electron-transfer bridge that promotes the separation of electron-hole pairs. Finally, pot experiments reveal that the P utilization efficiency for pepper seedlings fertilized by Pbi-ZnO-g-C3N4 is higher than that by Pbi-ZnO. The application of Pbi-ZnO-g-C3N4 is beneficial for the growth of native soil microorganism.

A new class of biochar-based slow-release phosphorus fertilizers with high water retention based on integrated co-pyrolysis and co-polymerization.

The development of slow-release phosphorus fertilizers (SRFs) with high water retention is of significance for modern agriculture. Herein, a new class of biochar-based SRFs are developed by an integrated co-pyrolysis and co-polymerization process (PSRFs). The water-retention performance and P slow-release behavior of PSRFs are evaluated, which are compared with other types of biochar-based SRFs derived from biochar-based phosphorus adsorption (MSRFs), co-pyrolysis of biomass-bentonite-nutrients (BSRFs), and the application of coating on BSRFs (CSRFs). The results show that the obtained PSRFs exhibits high water retention with the maximum swelling capacity of 94.2 g/g, far outstripping other tested SRFs. The water-retention performance of PSRFs is found to be positively correlated with their crosslinking agent contents. In addition, PSRFs has excellent P slow-release performance which is comparable with CSRFs (~51.5% of P release after 30 days), but much better than MSRFs and BSRFs with a complete P release after 30 days. Furthermore, pot experiments reveal that PSRFs has the highest P utilization efficiency (75.83% after 60 days), which can promote the growth of pepper seedlings better than other SRFs. Moreover, the soil burial tests indicate that PSRFs has a good biodegradability with the degradation ratio of 33.46% in 75 days. Finally, biological abundance analysis further reveals that Actinobacteria in soil is mainly responsible for the metabolism of starch and sodium alginate in PSRFs.

Trace metal elements mediated co-pyrolysis of biomass and bentonite for the synthesis of biochar with high stability.

The stability of biochar is a crucial parameter in determining the potential of biochar for carbon sequestration. Many studies have demonstrated that the addition of clay during the pyrolysis of biomass is beneficial for the production of biochar with a high stability, but finding a strategy for a further improvement of stability of clay-modified biochar is still highly desirable. Herein, the co-pyrolysis of biomass and clay mediated by trace metal elements is proposed as a new strategy for the production of biochar with exceptionally high stability. The results indicate that the biochar resistance index for biochar obtained from the trace metal elements mediated the co-pyrolysis of biomass and clay is ~0.75, which is much higher than that of biochars obtained from biomass pyrolysis or the co-pyrolysis of biomass and clay, demonstrating that the presence of metal ions during the co-pyrolytic process can significantly improve the oxidation resistance of biochar. Thermogravimetric analysis reveals that the carbon retention value is reduced when the addition of metal ions during the co-pyrolytic process, and the presence of metal ions can reduce the starting temperature of the pyrolysis reaction and catalyze the process of biomass pyrolysis. In addition, the percentages of CC, CC, and CH in all biochars obtained from trace metal elements mediated the co-pyrolysis of biomass and clay are greater than 41.82%, which are higher than that of original biochar. Besides, the percentage of oxygen-containing functional groups is found to be decreased after the presence of metal ions during the co-pyrolytic process. The presence of metal ions can form metal nano-sulfides and oxides on the surface, which plays a physical barrier to the anti-oxidation performance of biochar. Furthermore, compared to BBC or BC, MnBBC and ZnBBC have a better leaching resistance to P, while FeBBC has almost no leaching resistance to soil P. Overall, the study reveals that the addition of trace element metal ions during the co-prolysis of biomass and bentonite is an effective method to increase the stability of obtained biochar, and it is also beneficial for retarding the release of nutrients in the soil and thus increase the utilization of nutrients.

Biochar for simultaneously enhancing the slow-release performance of fertilizers and minimizing the pollution of pesticides.

Biochar has been extensively studied as a promising carrier material for fertilizers and an ideal adsorbent for the removal of pesticides. Yet, the application of biochar for simultaneously eliminating the pollution from the agricultural use of fertilizers and pesticides remains unexplored. Herein, we develop P-loaded biochar-based fertilizers (PBC) by the co-pyrolysis of cotton straw and H3PO4. The slow-release performance of PBC and their adsorption properties toward pesticides are investigated. The results indicate that the PBC leads to the improvement of adsorption performance, with the maximum adsorption capacities of lambda-cyhalothrin (LAC) for PBC and pristine biochar are 55.90 mg/g and 42.71 mg/g, respectively. Additionally, the adsorption of LAC is beneficial for the improvement of slow-release performance of PBC. The release ratios of P from PBC within 30 days reach 100.0% and 83.5% in water and LAC solution, respectively, demonstrating the existence of synergistic effects between the adsorption of pesticides and the slow release of nutrients. The mechanistic investigation reveals that the pretreatment of H3PO4 facilitates to activate more surface functional groups of PBC, contributing greatly to the improved adsorption of LAC. The adsorption of LAC reduces the BET of PBC with pore filling, enabling slower release rate of nutrients from PBC.

Microwave-assisted catalytic pyrolysis of apple wood to produce biochar: Co-pyrolysis behavior, pyrolysis kinetics analysis and evaluation of microbial carriers.

This studyinvestigated the behavior and kinetics of co-pyrolysis of apple wood (AW)with H3PO4and K3PO4as catalysts under microwaveto prepare biochar as microbialabsorbent. The kinetic studies indicate that the co-pyrolysis of AW withH3PO4orK3PO4can effectively improve the pyrolysis efficiencyand enhance the biocharcharacteristicsby reducing ofthe activation energy of the pyrolysis reaction. The kinetic parameters indicate that the activation energy of the mixturesin the main pyrolysis stage is lower than that of a single AW, whichmeanthat the co-pyrolysis of AW withH3PO4orK3PO4shows excellent synergy. Biochar characterization showed that the yield of biochar reachedthe highest58.6% whenthe ratio(H3PO4/AW) is0.5. The adsorption results show that the bacteria SL-44 can be effectively loaded on the surface of the biochar, and the adsorption process is combined with Langmuir model and process can proceed spontaneously.