Iron Nitrogen Research Articles

ZVI-biochar granules for reactive chlorinated solvent filters generated by high temperature pyrolysis of iron(III) amended biomass

Reactive filters may replace activated carbon filters for degradation of chlorinated solvents in contaminated waters. Reactive porous filter materials with high hydraulic conductivity may be in form of millimeter sized zero valent iron (ZVI)-biochar granules produced via carbothermal reduction. We screened ZVI-biochar materials produced under different synthesis conditions including different iron sources, nitrogen additives and supplementary organic substrates followed by testing adsorption and dechlorination kinetics. Diatomaceous earth was used as an inorganic host reference material. The optimal product from the screening was identified as beech charcoal amended with Fe(III) chloride and urea followed by tube furnace pyrolysis at 1000 °C for 2 h. The millimeter sized granules have a high porosity of 79 %. This material resulted in fast trichloroethylene (TCE, 100–600 µM) sorption and complete dechlorination with acetylene as the main product. It also showed a 5 to 8.5-fold higher degradation capacity than the diatomaceous earth reference system. Fitted pseudo first-order dechlorination rate constants (0.114–0.281 h−1) were comparable to rates reported for powdered ZVI-activated carbon materials. In reactions with high TCE concentrations, Fe(0) consumption for TCE reduction reached up to 93.3 % demonstrating its high selectivity. Reactions with ground material demonstrated that intraparticle diffusion pose minor limitation to dehalogenation rates in the highly porous granules. Further tests demonstrated that the material was further highly reactive to tetrachloroethylene (PCE), cis-1,2-dichloroethyene (cis-DCE) and vinyl chloride (VC). The ZVI-BC material addresses the dual challenges of achieving both high hydraulic conductivity and dehalogenation reactivity, offering a cost-efficient and sustainable option for filter material selection in the remediation of CEs using reactive filters or permeable reactive barriers.

Iron single atoms and nitrogen vacancies on graphitic carbon nitride synergically shallowing deep electron traps towards efficient photocatalytic ozonation

The coupling of photocatalysis and ozonation has been approved a very efficient strategy for hydroxyl radicals (•OH) production and wastewater decontamination, yet it remains challenging to enrich surface-reaching charges around reaction centers to accelerate this process. This paper explored the strategy of single-atoms (SAs) modification and defects control, aiming to enhance the activity of graphite carbon nitride (CN) in the visible light photocatalytic ozonation. It was found that the presence of iron SAs on CN greatly altered the impact of nitrogen vacancies (NVs), which behaved as recombination centers of photogenerated charge carriers and deteriorated activity of CN, while positively promoting the separation and migration of photogenerated carriers in the case for Fe-CNV (consist of iron SAs and NVs) catalysts. Based on photoluminescence (PL) emission, time-resolved PL spectra, ultrafast transient absorption spectroscopy and first-principles calculations, we found that adjacent iron SAs revived electrons trapped at NVs by elevating their energy level and mediating their interfacial transfer, leading to the decreased loss during electron transfer. This finding demonstrates the feasible tailor of energy level alignment for defect states to shallow deep electron traps.

Effects of the SmFeN content on the electromagnetic wave absorbing properties of sandwich-structured YSZ/SmFeN/YSZ composites

In this study, the thermal barrier material Yttria Stabilized Zirconia (YSZ) and the electromagnetic wave (EMW) absorbing agent samarium iron nitrogen (SmFeN) were used to prepare a YSZ/SmFeN/YSZ sandwich-structured composite. The YSZ/SmFeN interface was prepared perpendicular to the directions of EMWs. The EMW attenuation of the composites with different SmFeN contents and their mechanisms were studied using electromagnetic parameters, impedance matching, Cole–Cole circles, and minimum reflection loss (RLmin value). Dielectric loss was the dominant mechanism behind EMW attenuation for the composites. In addition, the dipole orientation of SmFeN and the presence of phase interface induced the dielectric loss. The mechanism of dipole orientation polarization was influenced by SmFeN content; the lesser the SmFeN content in the composite, the higher the ε′ (real part of dielectric coefficient). The frequency at which ε ′ peaked shifted decreased with increasing SmFeN content. Higher dielectric losses were observed in the frequency band of 4.0–8.0 GHz. The EMW absorption rate showed that the optimum EMW absorption effect was achieved when the thickness ratio of YSZ:SmFeN:YSZ was 1:4:1 and the thickness is 3.325 mm. The corresponding RLmin was −35.3 dB and effective absorption bandwidth was 9.5 GHz (8.3–17.9 GHz).

Gaseous Nitric Oxide As Probe Molecule for Fe-N-C ORR Electrocatalysts

Iron nitrogen carbon (Fe-N-C) electrocatalysts remain the most promising platinum group metal-free (PGM-free) catalysts for the oxygen reduction reaction (ORR) in polymer electrolyte fuel cells (PEFCs). Although significant progress has been made in recent years in improving both the ORR activity and stability of the Fe-N-C catalysts, further enhancement in the catalyst durability while maintaining the activity is imperative for the practical applications. One of the major factors that hinders the further enhancement of the catalysts is the lack of clear understanding of the nature of the active sites and density of the active sites in the Fe-N-C catalysts due to the complexity of the Fe-N-C catalysts’ composition and structure. Gaseous nitric oxide was proven to be a suitable probe molecule that can bond to Fe and impede the ORR of the Fe-N-C catalysts. In recent years, we have studied the effects of gas-phase adsorption and desorption of nitric oxide on the redox features and ORR activity on Fe-N-C catalysts synthesized by different methods. We have used various characterization tools to quantify the amount of nitric oxide adsorbed and to identify the adsorption sites and geometry, including electrochemical stripping, temperature programmed desorption, and in situ X-ray techniques. The corresponding results obtained will be summarized in this talk. The implication of these results on the nature of the ORR active sites of the Fe-N-C catalysts will be discussed.AcknowledgementsThis work was supported by the U.S. Department of Energy (DOE), Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office (HFTO) under the auspices of the Electrocatalysis Consortium (ElectroCat 2.0). This work utilized the resources of the Advanced Photon Source, a U.S. DOE Office of Science user facility operated by Argonne National Laboratory for DOE Office. This work was partially authored by Argonne, a U.S. Department of Energy (DOE) Office of Science laboratory operated for DOE by UChicago Argonne, LLC under contract no. DE-AC02-06CH11357.

Synergistic mechanisms of denitrification in FeS2-based constructed wetlands: Effects of organic carbon availability under day-night alterations

In constructed wetlands (CWs), carbon source availability profoundly affected microbial metabolic activities engaged in both iron cycle and nitrogen metabolism. However, research gaps existed in understanding the biotransformation of nitrogen and iron in response to fluctuations in organic carbon content under day-night alterations. Results demonstrated increased removal efficiency of NO3−-N (95.7 %) and NH4+-N (75.70 %) under light conditions, attributed to increased total organic carbon (TOC). This enhancement promoted the relative abundance of bacteria involved in nitrogen and iron processes, establishing a more stable microbial network. Elevated TOC content also upregulated genes for iron metabolism and glycolysis, facilitating denitrification. Spearman correlation analysis supported the synergistic mechanisms between FeS2-based autotrophic denitrification and TOC-mediated heterotrophic denitrification under light conditions. The significant impact of carbon sources on microbial activities underscores the critical role of organic carbon availability in enhancing nitrogen removal efficiency, providing valuable insights for optimizing FeS2-based CWs design and operation strategies.

Using Iron L-Edge and Nitrogen K-Edge X-ray Absorption Spectroscopy to Improve the Understanding of the Electronic Structure of Iron Carbene Complexes.

Iron-centered N-heterocyclic carbene compounds have attracted much attention in recent years due to their long-lived excited states with charge transfer (CT) character. Understanding the orbital interactions between the metal and ligand orbitals is of great importance for the rational tuning of the transition metal compound properties, e.g., for future photovoltaic and photocatalytic applications. Here, we investigate a series of iron-centered N-heterocyclic carbene complexes with +2, + 3, and +4 oxidation states of the central iron ion using iron L-edge and nitrogen K-edge X-ray absorption spectroscopy (XAS). The experimental Fe L-edge XAS data were simulated and interpreted through restricted-active space (RAS) and multiplet calculations. The experimental N K-edge XAS is simulated and compared with time-dependent density functional theory (TDDFT) calculations. Through the combination of the complementary Fe L-edge and N K-edge XAS, direct probing of the complex interplay of the metal and ligand character orbitals was possible. The σ-donating and π-accepting capabilities of different ligands are compared, evaluated, and discussed. The results show how X-ray spectroscopy, together with advanced modeling, can be a powerful tool for understanding the complex interplay of metal and ligand.

Comparative genomic analysis of Bacillus atrophaeus HAB-5 reveals genes associated with antimicrobial and plant growth-promoting activities.

Bacillus atrophaeus HAB-5 is a plant growth-promoting rhizobacterium (PGPR) that exhibits several biotechnological traits, such as enhancing plant growth, colonizing the rhizosphere, and engaging in biocontrol activities. In this study, we conducted whole-genome sequencing of B. atrophaeus HAB-5 using the single-molecule real-time (SMRT) sequencing platform by Pacific Biosciences (PacBio; United States), which has a circular chromosome with a total length of 4,083,597 bp and a G + C content of 44.21%. The comparative genomic analysis of B. atrophaeus HAB-5 with other strains, Bacillus amyloliquefaciens DSM7, B. atrophaeus SRCM101359, Bacillus velezensis FZB42, B. velezensis HAB-2, and Bacillus subtilis 168, revealed that these strains share 2,465 CDSs, while 599 CDSs are exclusive to the B. atrophaeus HAB-5 strain. Many gene clusters in the B. atrophaeus HAB-5 genome are associated with the production of antimicrobial lipopeptides and polypeptides. These gene clusters comprise distinct enzymes that encode three NRPs, two Transat-Pks, one terpene, one lanthipeptide, one T3PKS, one Ripp, and one thiopeptide. In addition to the likely IAA-producing genes (trpA, trpB, trpC, trpD, trpE, trpS, ywkB, miaA, and nadE), there are probable genes that produce volatile chemicals (acoA, acoB, acoR, acuB, and acuC). Moreover, HAB-5 contained genes linked to iron transportation (fbpA, fetB, feuC, feuB, feuA, and fecD), sulfur metabolism (cysC, sat, cysK, cysS, and sulP), phosphorus solubilization (ispH, pstA, pstC, pstS, pstB, gltP, and phoH), and nitrogen fixation (nif3-like, gltP, gltX, glnR, glnA, nadR, nirB, nirD, nasD, narl, narH, narJ, and nark). In conclusion, this study provides a comprehensive genomic analysis of B. atrophaeus HAB-5, pinpointing the genes and genomic regions linked to the antimicrobial properties of the strain. These findings advance our knowledge of the genetic basis of the antimicrobial properties of B. atrophaeus and imply that HAB-5 may employ a variety of commercial biopesticides and biofertilizers as a substitute strategy to increase agricultural output and manage a variety of plant diseases.

Optimization of “sulfur–iron–nitrogen” cycle in constructed wetlands by adjusting siderite/sulfur (Fe/S) ratio

Sulfur-siderite autotrophic denitrification (SSAD) has been proved to solve the key problem of low nitrogen removal efficiency caused by the shortage of carbon source in constructed wetlands (CWs). In this study, five vertical flow constructed wetlands (VFCWs) were constructed with different Fe/S ratios (0/0, 0/1, 1/1, 2/1 and 1/2) to optimizing SSAD process, labeled S.0, S.1, S.2, S.3 and S.4. The results showed that the best NO3−-N and TN removal rates were achieved with a Fe/S ratio of 2:1 (S.3), which were 96.26 ± 1.40% and 93.63 ± 3.12%, respectively. The abundance of denitrification genes (nirS, nirK and nosZ) in S.3 was significantly increased. Illumina high-throughput sequencing analysis indicated that the abundance and diversity of microorganisms involved in the “Sulfur–Iron–Nitrogen” cycle were enriched in S.3. The current study provided that the “Sulfur–Iron–Nitrogen” cycle in CWs was optimized by adjusting Fe/S ratio, and more types of denitrifying bacteria could be enriched, thereby enhancing nitrogen removal.

Mapping Degradation of Iron–Nitrogen–Carbon Heterogeneous Molecular Catalysts with Electron-Donating/Withdrawing Substituents

Mapping Degradation of Iron–Nitrogen–Carbon Heterogeneous Molecular Catalysts with Electron-Donating/Withdrawing Substituents

Simultaneous removal of nitrogen, phosphorus, and organic matter from oligotrophic water in a system containing biochar and construction waste iron: Performances and biotic community analysis

The issue of combined pollution in oligotrophic water has garnered increasing attention in recent years. To enhance the pollutant removal efficiency in oligotrophic water, the system containing Zoogloea sp. FY6 was constructed using polyester fiber wrapped sugarcane biochar and construction waste iron (PWSI), and the denitrification test of simulated water and actual oligotrophic water was carried out for 35 days. The experimental findings from the systems indicated that the removal efficiencies of nitrate (NO3–−N), total nitrogen (TN), chemical oxygen demand (COD), and total phosphorus (TP) in simulated water were 88.61%, 85.23%, 94.28%, and 98.90%, respectively. The removal efficiencies of actual oligotrophic water were 83.06%, 81.39%, 81.66%, and 97.82%, respectively. Furthermore, the high−throughput sequencing data demonstrated that strain FY6 was successfully loaded onto the biological carrier. According to functional gene predictions derived from the Kyoto Encyclopedia of Genes and Genomes (KEGG) database, the introduction of PWSI enhanced intracellular iron cycling and nitrogen metabolism.

Single-atom Fe catalysts with pyrrolic-type FeN4 sites for efficient oxygen reduction reaction: Identifying the roles of different N species

Developing electrocatalysts with efficient cathode oxygen reduction reaction (ORR), for example, iron-based single-atom catalysts (Fe-SACs), has been deemed necessary to accelerate the commercialisation process of zinc (Zn)–air batteries. Nevertheless, determining how various nitrogen species and active metal centres coordinate on an atomic scale remains unclear and inadequately explained. Herein, we demonstrate a soft-template-aided technique using Fe-containing molecules (e.g. iron phthalocyanine [FePc], Fe-1,10-phenanthroline [Fe-Phen] and Fe-glucose) to enhance the performance of Fe-SACs in terms of ORR. In this technique, FePc molecules can be converted into atomically dispersed pyrrolic-type iron–nitrogen (FeN4) sites during a pyrolytic process. The resultant catalyst exhibits excellent ORR activity (half-wave potential = 0.90 V) in alkaline medium and standing battery performance when used in Zn–air batteries (peak power density = 197.3 mW cm−2 and specific capacity = 796.2 mAh g−1). As per the findings from control experiments and characterisation studies, electron transfer between the support and the active Fe centre amplifies the ORR performance. Theoretical calculations substantiate that Fe sites coordinated with pyrrolic N atoms govern the electronic configuration of the catalysis, reducing the free energy absorption of reaction intermediates and thus increasing its intrinsic ORR capability. Herein, we aim to offer a fresh perspective on the relation between coordination environments and catalytic activity in ORR catalysts.

The effects of phase interfaces in SmFeN/YSZ composite thermal barrier materials on electromagnetic wave-absorbing properties

Yttria-stabilized zirconia (YSZ) oxide ceramic powder is a thermal-barrier material used to fabricate thermal barrier coatings (TBC). In this study, to improve the electromagnetic wave (EMW) absorbing properties of TBCs, microwave-absorbing samarium iron nitrogen (SmFeN) particles were used to prepare SmFeN/yttria-stabilized zirconia (YSZ) composites. To study the effect of the SmFeN/YSZ interfaces on the EMW-absorbing properties of the SmFeN/YSZ composite, SmFeN/YSZ interfaces were built in different ways in composite materials having the same mass ratio of 1:1, for example, SmFeN and YSZ particles homogeneously mixed together, SmFeN/YSZ interfaces perpendicular and parallel to the EMW incident direction, and different interfaces between YSZ and SmFeN. Thus, the microwave absorbing performance of the samples, including the electromagnetic parameters, attenuation coefficient, eddy-loss current (C0), impedance matching, and minimum reflection loss (RLmin) values were examined and analyzed. The results demonstrate that interfaces perpendicular to the direction of the EMWs can increase the contact area and enhance the interfacial absorption effect. Further, when the wave-absorbing agent was placed in the middle of the composite, its wave-absorbing effect was the best among all the samples, yielding RLmin = −27.824 dB and effective absorption bandwidth (EAB) = 8.5453 GHz (effective absorption frequency range 7.9256–16.4709 GHz for a 7.2-mm-thick layer). Crucially, the frequency and bandwidth at which the best absorption occurred could be tuned by adjusting the thickness of the coating. This is because the interfaces in the samples resulted in polarization enhancement and anomalous dispersion, leading to large dielectric losses. Overall, the use of a coaxial measurement technique is highly efficient for EMW absorbing body design and process simulations.

Toxic effects of nanoplastics on biological nitrogen removal in constructed wetlands: Evidence from iron utilization and metabolism

Nanoplastics (NPs) in wastewaters may present a potential threat to biological nitrogen removal in constructed wetlands (CWs). Iron ions are pivotal in microbially mediated nitrogen metabolism, however, explicit evidence demonstrating the impact of NPs on nitrogen removal regulated by iron utilization and metabolism remains unclear. Here, we investigated how NPs disturb intracellular iron homeostasis, consequently interfering with the coupling mechanism between iron utilization and nitrogen metabolism in CWs. Results indicated that microorganisms affected by NPs developed a siderophore-mediated iron acquisition mechanism to compensate for iron loss. This deficiency resulted from NPs internalization limited the activity of the electron transport system and key enzymes involved in nitrogen metabolism. Microbial network analysis further suggested that NPs exposure could potentially trigger destabilization in microbial networks and impair effective microbial communication, and ultimately inhibit nitrogen metabolism. These adverse effects, accompanied by the dominance of Fe3+ over certain electron acceptors engaged in nitrogen metabolism under NPs exposure, were potentially responsible for the observed significant deterioration in nitrogen removal (decreased by 30 %). This study sheds light on the potential impact of NPs on intracellular iron utilization and offers a substantial understanding of the iron-nitrogen coupling mechanisms in CWs.

Promoting denitrification via high electron conversion ratio in the iron valence Cycle: Prospects for Pseudomonas sp. JM-7 application in environmental engineering

The interdependence between iron and nitrogen in the environment is of utmost importance, and this study has explored the intricate relationship between denitrification and iron valence cycling using Pseudomonas sp. strain JM-7 (P. JM-7) as a model bacteria. Our research demonstrated that P. JM-7 had the ability to effectuate electron transfer from the periplasmic space to electron acceptors, such as nitrate, via Cytochrome c-proteins (c-Cyts). We found that iron valence state transformations with Fe(II)/Fe(III) promoted P. JM-7′s denitrification of nitrate coupled to yeast extract powder (YEP) oxidation. Denitrification rates depended on temperature (>21 °C) and pH (6–9). During logarithmic growth, 5 g/L YEP enabled 350 mg/L nitrate removal, increasing to 1650 mg/L in stable growth. Addition of 4 mM Fe(II)/Fe(III) increased denitrification to 500 mg/L during logarithmic growth. The dynamic test results displayed that compared to the SiO2 filler control group, iron-containing fillers could facilitate P. JM-7 to reduce 100 mg/L nitrate with 50 mg/L YEP electrons, corresponding to 6 times the maximum electron transfer efficiency in the static test. Overall, iron redox cycling significantly enhanced P. JM-7 denitrification, imparting insights into iron–nitrogen interactions. In summary, our research imparts valuable insights into the nexus between iron and nitrogen in the environment, highlighting the potential application of P. JM-7 in environmental engineering. Our findings indicate that P. JM-7 exhibits a significant denitrification capability, and further research is recommended to investigate its ability to remove phosphorus and promote sustainable environmental remediation practices.

Optimizing particle morphology: Atomic iron–nitrogen centers with graphitic‐N for highly efficient CO2 electroreduction

AbstractTransition metal‐coordinated nitrogen sites on carbon catalysts (M‐N‐C) hold potential for CO2 electroreduction (CO2ER), but optimal morphology and active sites are unclear. We introduce a novel approach, developing zeolitic imidazolate framework‐8 (ZIF‐8)‐derived carbon catalysts with Fe‐N and graphitic‐N sites (Fe2‐NC) via molecular confinement and thermal activation. Fine‐tuning ZIF‐8 size and activation temperature yielded 44.98% active N sites. The 300 nm Fe2‐NC catalyst displayed outstanding CO2‐to‐CO conversion, with a 170 mV overpotential and 94.3% Faradaic efficiency at −0.5 V, outperforming state‐of‐the‐art materials. Enhanced CO2ER kinetics and conductivity contributed to this superiority. Results highlight the correlation between maximum CO Faradaic efficiency and cumulative Fe‐N/graphitic‐N sites, dependent on size and activation. The 300 nm Fe2‐NC in a gas diffusion electrode‐loaded flow cell achieved a 15.3‐fold CO partial current density increase. In a Zn‐CO2 battery, the 300 nm Fe2‐NC demonstrated a peak power density of 0.618 mW cm−2, showcasing energy storage potential.

Mesoporous Single Atom-Cluster Fe-N/C Oxygen Evolution Electrocatalysts Synthesized with Bottlebrush Block Copolymer-Templated Rapid Thermal Annealing.

Current electrocatalysts for oxygen evolution reaction (OER) are either expensive (such as IrO2, RuO2) or/and exhibit high overpotential as well as sluggish kinetics. This article reports mesoporous earth-abundant iron (Fe)-nitrogen (N) doped carbon electrocatalysts with iron clusters and closely surrounding Fe-N4 active sites. Unique to this work is that the mechanically stable mesoporous carbon-matrix structure (79 nm in pore size) with well-dispersed nitrogen-coordinated Fe single atom-cluster is synthesized via rapid thermal annealing (RTA) within only minutes using a self-assembled bottlebrush block copolymer (BBCP) melamine-formaldehyde resin composite template. The resulting porous structure and domain size can be tuned with the degree of polymerization of the BBCP backbone, which increases the electrochemically active surface area and improves electron transfer and mass transport for an effective OER process. The optimized electrocatalyst shows a required potential of 1.48 V (versus RHE) to obtain the current density of 10 mA/cm2 in 1 M KOH aqueous electrolyte and a small Tafel slope of 55 mV/decade at a given overpotential of 250 mV, which is significantly lower than recently reported earth-abundant electrocatalysts. Importantly, the Fe single-atom nitrogen coordination environment facilitates the surface reconstruction into a highly active oxyhydroxide under OER conditions, as revealed by X-ray photoelectron spectroscopy and in situ Raman spectroscopy, while the atomic clusters boost the single atoms reactive sites to prevent demetalation during the OER process. Density functional theory (DFT) calculations support that the iron nitrogen environment and reconstructed oxyhydroxides are electrocatalytically active sites as the kinetics barrier is largely reduced. This work has opened a new avenue for simple, rapid synthesis of inexpensive, earth-abundant, tailorable, mechanically stable, mesoporous carbon-coordinated single-atom electrocatalysts that can be used for renewable energy production.

Comparative Reports on Pleurotus Sajor-caju Cultivated on Local Wood Wastes in Ibadan Metropolis, Nigeria

Cultivation of Pleurotus species, an Oyster mushroom is now becoming well known due to its taste, medicinal and nutritional values. It is capable of degrading agricultural wastes efficiently and even grows at different temperature ranges. Relatively, Pleurotus species has shorter life span and the fruiting bodies are rarely attacked by pests and diseases unlike the other edible mushrooms. Therefore, the aim of this research is to access the influence of mineral constituents of five local wood wastes (Anogeissus leiocarpa, Pouteria altissima, Vitellaria paradoxa, Cordia milleni and Triplochiton scleroxylon) in Ibadan metropolis on the growth, fruiting body yield and proximate analysis of cultivated oyster mushroom (P. sajor-caju). Data of Carbon/Nitrogen ratio (11.10 – 11.60) found reveal composition of Magnesium (0.035 mg), Potassium (0.053 mEq/l), Manganese (0.0013 mg), Copper (0.00050 g/m3), Iron (0.00275 mol/L), Phosphorus (0.027 mmol/L), Organic carbon (32.10 mg/L C), Organic matter (55.3 t/ha) and total nitrogen (2.77 mg/L) contributed greatly to the high crude protein, fats and ash contents of mushroom cultivated on T. Scleroxylon. However, insignificant contents of sodium (0.2 mg), Calcium (0.2 mmol/L) and Magnesium (0.013 mg) in Pouteria altissima led to the general inadequate performance of (P. sajor-caju) in yields. The fresh mean weight of (P. sajor-caju) was from 8.00 g – 27.53 g. The heaviest weight was obtained from T. scleroxylon followed by V. paradoxa, C. milleni, while Anogeissus leiocarpa gave the lightest weight. Hence, T. scleroxylon will be suggested for cultivating P. sajor-caju because of its positive impact on the yield, crude fibre, and protein content of the experimented mushroom.

A novel γ-Fe3O4-N-BC combined membrane bioreactor for wastewater treatment: Performance and mechanism

In this study, a new type of iron–nitrogen doped biochar (γ- Fe3O4-N-BC) was developed to improve nutrient removal efficiency and mitigate membrane fouling in combination with MBR. The characteristion of γ-Fe3O4-N-BC, N-BC, and BC revealed that the BET surface area (SBET) of γ-Fe3O4-N-BC, which was 1320.86 m2/g, was greater than that of N-BC (702.75 m2/g) and BC (1033.63 m2/g). The excellent SBET exhibited by γ-Fe3O4-N-BC compared to that of the other biochars is attributed to hydrogen bonding and electrostatic interactions. Compared to the addition of N-BC or BC or the absence of biochar, the addition of γ-Fe3O4-N-BC in the membrane bioreactor (MBR) resulted in superior wastewater treatment performance, for which the average removal efficiencies of chemical oxygen demand (COD), ammonia nitrogen (NH4+-N), and total phosphorus (TP) were 94.65 %, 82.56 %, and 65.90 %, respectively. Moreover, after inoculation with γ-Fe3O4-N-BC, the TMP increase rate and time required to reach 42.37 kPa were 2.35 kPa/d and 18 d, respectively. The investigation of the effect of the γ-Fe3O4-N-BC concentration on MBR performance showed that the nutrient removal efficiency in the 500-MBR greater than that in the 350-MBR, 650-MBR, and 800-MBR, and that the membrane fouling was more ameliorative. A mechanistic investigation demonstrated that the 500-MBR had a beneficial influence on sludge biomass growth and helped to improve the nutrient removal capacity of the MBR. The 500-MBR improved the flocculability and stability of the sludge flocs in the MBR by increasing particle size and zeta potential. Changes in the extracellular polymeric substance (EPS) concentration and the smaller protein (PN) / polysaccharide (PS) ratio in 500-MBR also had significant impacts on alleviating the adhesion and accumulation of fouling layers on the improved membrane surface. Consequently, this study provides a new method for nutrient removal and membrane fouling mitigation in the MBR process.

GREEN CHEMISTRY: USING MORE SUSTAINABLE TECHNIQUES TO ESTIMATE THE WATER QUALITY OF THE UBERABA RIVER USING ORBITAL OPTICAL SENSORS

Green Chemistry aims to prevent pollution resulting from activities in the chemical sector. Generally, laboratory activities generate pollution because toxic substances are used to perform analyses, which produce waste once the analyses are completed. This study aimed to monitor the quality of the Uberaba River using more sustainable and non-destructive techniques through orbital remote sensing and to develop methods for estimating water quality at reduced costs using orbital sensors and machine learning. The values of water quality parameters, such as iron, nitrate, chloride, total phosphorus, and total nitrogen, were studied between 2018 and 2023. Orbital sensing data (spectral bands and vegetation indices) were taken from the exact geographic coordinates of the collection points. Data were analyzed using Pearson’s correlation coefficient and random forest regression analysis. The study concludes that it is possible to perform orbital remote sensing by estimating water quality through random forest regression, correlating the information obtained from Sentinel-2 images with the values of these parameters. This approach is a sustainable technique that does not generate waste and represents a 100% saving compared to conventional chemical analyses.

Sulfur-assisted ammonia treatment of a fibrous carbon matrix to fabricate a high-content pyrrole-type Fe–N–C catalyst for superior oxygen reduction

High-content pyrrole-type iron–nitrogen–carbon sites on a fibrous carbon matrix were successfully prepared through ammonia treatment with pre-doping of sulfur, which shows excellent performance toward the oxygen reduction reaction.