Sustainable Treatment Research Articles

Role of molybdenum compounds in enhancing denitrification: Structure-activity relationship and the regulatory mechanisms

The effect and regulatory mechanisms of molybdenum compounds (MoO2, MoS2, MoSe2 and MoSi2) on denitrification were investigated by structure-activity relationships, electrochemical characteristics, microbial metabolism analysis and bacterial community distribution. All the assessed molybdenum compounds exhibited the enhancement effect on denitrification, in the order of MoS2 > MoSi2 > MoSe2 > MoO2, with MoS2 increasing 7.08-fold in 12 h. Analysis of structure-activity relationships suggested that the molybdenum compounds with lower negative redox potential and higher redox reversibility were favorable for promoting denitrification. According to the morphology observation, the interactions between Mo compounds and denitrifying bacteria may be beneficial to extracellular electron transfer. Molybdenum compounds with electron transfer capability facilitated an increase in electron capacitance from 835.1 to 1011.3 μF, promoting the electron exchange rate during denitrification. In the denitrification electron transport chain, the molybdenum compounds upregulated nicotinamide adenine dinucleotide and denitrifying enzyme activity, as well as facilitated the abundance of quinone pools, ATP translocation, and cytochrome c related proteins. Moreover, Mo compounds enriched functional bacteria such as electroactive bacteria and denitrifying functional bacteria. Notably, Mo ions in molybdenum compounds may provide active sites for nitrate reductase, optimizing the electron distribution of the denitrification process and thus improved the partial denitrification efficiency. This work aimed to further understand the regulatory mechanisms of molybdenum on denitrification electron transfer in the compound state and to anticipate the catalytic role of Mo compounds for sustainable water treatment.

Selective electro-induced reduction using bionic BC@SA-Nafion particle electrodes in 3D systems and phytotoxicity assessment

Three-dimensional electrode technology (3D technology), featuring dispersed particulate electrodes is rapidly advancing in the separation of pollutants. However, in contrast to the electrochemical oxidation performance, the design of particulate electrodes for electrochemical reduction remains relatively underexplored. This study introduced a bionic particle electrode (BC@SA-Nafion) with high reducibility and selectivity, and integrated it into a 3D system. Specifically, the selective electro-induced reduction capacity of BC@SA-Nafion was examined using Cr(Ⅵ) as a model pollutant. The electrochemical reactivity of BC@SA-Nafion was found to be dependent on the amount of biochar (BC) incorporated. Furthermore, the selectivity for Cr(Ⅵ) could be fine-tuned by adjusting the Nafion content, thereby addressing the efficiency decline at lower Cr(Ⅵ) concentrations. In the 3D system, the Cr(Ⅵ) removal rate reached up to 99 % under optimal conditions (pH 2, 2 V cm−1, 30 min). The density functional theory calculations indicated that the selectivity of BC@SA-Nafion for Cr(Ⅵ) was dependent on the presence of fluorine bonds. The reduction of Cr(Ⅵ) mainly relied on direct electron transfer provided, with superoxide (·O- 2) also playing a role. Post-treatment with the 3D technology resulted in negligible phytotoxicity of the wastewater. This study introduced a novel strategy for enhancing the selectivity of particle electrodes, thereby expanding the application of the particle electrode and advancing sustainable water treatment technologies.

Selective adsorption of cationic dye by κ-carrageenan-potato starch bio-hydrogel: Kinetics, isotherm, and thermodynamic studies

An eco-friendly κ-carrageenan/potato starch bio-hydrogel is designed for the efficient removal of methylene blue (MB) dye from water. The incorporation of potato starch was successfully confirmed through XRD, FT-IR, and SEM analysis, while TGA highlighted the hydrogel's thermal stability. Batch adsorption experiments demonstrated excellent MB removal efficiency, with a maximum adsorption capacity of 116.1 mg/g under optimal conditions (initial dye concentration: 100 mg/L, contact time: 180 min, temperature: 20 °C, adsorbent dosage: 1.6 g/L, and pH: 11). FT-IR analysis indicated that electrostatic interactions and hydrogen bonding primarily govern the adsorption process. The adsorption followed pseudo-second-order kinetics and fitted well with the Langmuir isotherm model. Thermodynamic studies revealed that the adsorption was exothermic and spontaneous. A key feature of this bio hydrogel is its selective affinity for the cationic dye MB, in a mixture with Acid Orange (AO) and other cationic dyes (Rhodamine B (Rh B) and crystal violet (CV)). The adsorbent also demonstrated impressive reusability, maintaining 93 % of its efficiency after five cycles, highlighting its potential for sustainable and cost-effective water treatment.

A novel BiVO4/vermiculite Z-scheme heterojunction with enhanced removal rate of dyes through adsorption photodegradation synergistic mechanism

Water pollution, exacerbated by industrialization, poses severe threats to aquatic ecosystems and human health, particularly due to persistent organic pollutants like dyes. To mitigate this issue, the development of effective and sustainable water treatment technologies is essential. This study presents the synthesis of a novel bismuth vanadate (BVO)/vermiculite (Vt) adsorption-photocatalytic self-cycling composite using a simple hydrothermal method. The composite's Z-scheme heterojunction structure, along with the introduction of surface oxygen vacancies, significantly reduces electron-hole recombination and enhances charge separation. These modifications lead to a 1.64-fold increase in adsorption capacity compared to Vt and a 6.4-fold improvement in photocatalytic efficiency over BVO. The material maintained a 76 % removal efficiency after five usage cycles and demonstrated high efficacy in methylene blue (MB) solutions, even at concentrations up to 300 mg/L. Moreover, the composite displayed stable performance under repeated use and in high-pollutant environments, highlighting its durability and practicality. These characteristics underscore its strong potential for widespread application in environmental remediation and sustainable water resource management, offering an innovative solution to the global challenge of water pollution.

Photocatalyst immobilisation on cylindrical surface: Scale-up potential of continuous photocatalytic reactor

The use of continuous photocatalytic reactor is important for sustainable water treatment technology. Photocatalyst immobilisation on supports (of varying shapes and sizes) having the desired degree of uniformity and smoothness is challenging, and is evolving. The major concerns are the geometry of the surface (which restricts the scalability of such systems) and the appropriate adhesion of the photocatalyst. Flat surface has an inherent limitation of low photocatalyst area per floor space, and poor light distribution, whereas cylindrical surfaces can overcome all these limitations. In this work, we have developed and assessed the photocatalyst coating methodology over cylindrical (quartz) surface and have prepared a modular (continuous) photocatalytic reactor. We have immobilised titanium-dioxide on the outer surface of a cylindrical quartz tube using a rotating (coating) mechanism, using the viscous sol prepared from the sol-gel method followed by heat treatment, and not with any binder to the as-synthesized powder. Various characterization techniques, including ultraviolet-diffuse reflectance spectroscopy, energy-dispersive spectroscopy, x-ray diffraction, field-emission scanning electron microscopy, optical surface profilometry, and ultraviolet–visible spectroscopy, are used to evaluate the impact of process conditions – number of layers, rotational speed, and sol viscosity, on the coating uniformity, smoothness, and layer thickness. The performance of the custom-made (modular-type) reactor is evaluated for degradation of the model molecule (pollutant). The reactor performance and capacity can be easily scaled up by parallel connections or introducing multiple coated tubes (to increase the photocatalyst area). The outcome of the work will be of immense value in scaling up the continuous large scale photocatalytic operation and treatment process.

Directional Electron Transfer in Enzymatic Nano‐Bio Hybrids for Selective Photobiocatalytic Conversion of Nitrate

Semi‐artificial photosynthetic system (SAPS) that combines enzymes or cellular organisms with light‐absorbing semiconductors, has emerged as an attractive approach for nitrogen conversion, yet faces the challenge of reaction pathway regulation. Herein, we find that photoelectrons can transfer from the ‐C≡N groups at the edge of cyano‐rich carbon nitride (g‐C3N4‐CN) to nitrate reductase (NarGH), while the direct electron transfer to nitrite reductase (cd1NiR) is inhibited due to the physiological distance limit of active sites (> 14 Å). By means of the directional electron transfer between g‐C3N4‐CN and extracted biological enzymes, the product of the denitrification reaction was switched from inert N2 to usable nitrite with an unprecedented selectivity of up to 95.3%. The converted nitrite could be further utilized by anammox microbiota and dissimilatory nitrate reduction to ammonia (DNRA) microorganisms, doubling the efficiency of total nitrogen removal (96.5 ± 2.3 %) for biological nitrogen removal and ammonia generation (12.6 mg NH4+‐N L‐1 h‐1), respectively. Thus, our work paves an appealing way for the sustainable treatment and utilization of nitrate for ammonia fuel production by strategically regulating the electron transfer pathway across the biotic‐abiotic interface.

Microbial Degradation of Polyester Microfibers Using Indigenously Isolated Bacterial Strain Exiguobacterium Sp.

ABSTRACTSynthetic microfibers are emerging environmental microplastic pollutants released from different industrial and domestic sources. The present investigation describes the isolation of potential bacterial strains from microplastic‐contaminated sites of Bhubaneswar city of Odisha, India. Four morphologically distinct bacterial strains were isolated using 2% polyethylene glycol (PEG) supplemented nutrient agar (NA) medium and were screened for their polymer tolerance ability by growing them on 2%–8% PEG. A single microorganism capable of growing on 8% PEG was selected for biodegradation experiment. Through 16S rRNA sequencing, the selected bacterial strain was identified as Exiguobacterium sp. with gene bank accession number ON318396. The microbial strain's microfiber biodegradation ability was assessed in a laboratory setting over a period of 28 ± 2 days, utilizing optimized conditions with an initial pH of 7, 2 mL inoculum volume, an incubation temperature of 30°C ± 2°C, and 150 rpm, using 2 g of polyester microfiber. In optimum conditions, the weight loss of the treated sample with the selected microbial strain was 19.2%. The polyester degradation was confirmed through scanning electron microscopic images viewing the degradation of the polyester microfiber surfaces. Variation in functional groups confirmed through Fourier transform infrared spectrophotometry. Detection of carbonyl (C═O) group stretching band at 1711 cm−1 through ATR‐FTIR analysis in the treated sample confirmed the polymer biodegradation. The potential isolate can efficiently degrade polyester and, in the future, can be employed as a promising solution for the sustainable treatment of synthetic microfiber pollution.

Directional Electron Transfer in Enzymatic Nano-Bio Hybrids for Selective Photobiocatalytic Conversion of Nitrate.

Semi-artificial photosynthetic system (SAPS) that combines enzymes or cellular organisms with light-absorbing semiconductors, has emerged as an attractive approach for nitrogen conversion, yet faces the challenge of reaction pathway regulation. Herein, we find that photoelectrons can transfer from the -C≡N groups at the edge of cyano-rich carbon nitride (g-C3N4-CN) to nitrate reductase (NarGH), while the direct electron transfer to nitrite reductase (cd1NiR) is inhibited due to the physiological distance limit of active sites (> 14 Å). By means of the directional electron transfer between g-C3N4-CN and extracted biological enzymes, the product of the denitrification reaction was switched from inert N2 to usable nitrite with an unprecedented selectivity of up to 95.3%. The converted nitrite could be further utilized by anammox microbiota and dissimilatory nitrate reduction to ammonia (DNRA) microorganisms, doubling the efficiency of total nitrogen removal (96.5 ± 2.3 %) for biological nitrogen removal and ammonia generation (12.6 mg NH4+-N L-1 h-1), respectively. Thus, our work paves an appealing way for the sustainable treatment and utilization of nitrate for ammonia fuel production by strategically regulating the electron transfer pathway across the biotic-abiotic interface.

Alginate/CuO-gC3N4 composite: a novel, reusable, non-toxic photocatalyst for methylene blue degradation.

Increasing industrial contamination necessitates development of sustainable water treatment solutions. Photocatalysis is a green technology utilizing light-activated materials (photocatalysts), which can degrade pollutants into harmless by-products. It is an emergent need to develop a photocatalyst that presents a significant advancement for sustainable water treatment and non-toxic to the environment. This study investigates the photocatalytic activity and in vitro cytotoxicity of a novel hybrid material comprising of alginate, copper oxide (CuO) and graphitic carbon nitride (gC3N4) for methylene blue (MB) degradation. The hybrid material was synthesized by a two-step process: (i) doping of CuO on gC3N4 through co-precipitation method formed CuO-gC3N4 (CG) and (ii) incorporation of CG in the calcium alginate (A) by ionotropic gelation method that is named as ACG. The characteristic features of the synthesized A, CG and ACG were studied using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The optical characteristic of A, CG and ACG was studied using UV-diffuse reflectance spectroscopy (UV-DRS). The morphology and elemental composition of ACG was evaluated by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). To assess the environmental impact of ACG, a two-step approach was employed. First, the photocatalytic activity of ACG under UV-visible light (UV-vis) irradiation for MB degradation was evaluated. ACG exhibited photocatalytic activity by achieving 86.26% of degradation efficiency for MB within 60min. Second, the in vitro cytotoxicity of ACG, MB and MB degraded products towards tilapia gill cell lines were assessed. By comparing the toxicity of the MB and the secondary products, it is concluded that the overall process leads to a sustainable outcome.

Environmental sustainable treatment and disposal technologies for reservoir wastes: a review.

The process of dredging reservoirs serves the purpose of preserving water storage capacity and ensuring the functionality of navigational channels. Additionally, it has the potential to mitigate the presence of pollutants and chemicals that pose risks to both the environment and human well-being. This review article examines the many ways of disposal and treatment of dredged sediment, as well as the ecological and economic advantages associated with these approaches. Algae and reed-based treatment methods have the potential to effectively and economically remediate and sustainably manage dredged sediments. Landfills and ocean dumping are widely utilized methods for the disposal of excavated materials. However, other approaches such as land reclamation, the use of fill material, and the preservation of wetlands can offer cost-effective solutions while also contributing to environmental conservation. The implementation of sediment cleaning, stabilization, and solidification techniques has the potential to effectively mitigate waste and improve the quality of sediment, hence facilitating its reuse. Algae and reed-based treatment systems have been found to effectively mitigate disposal costs and contribute to environmental enhancement. Additionally, the practice of reusing dredged sediments has been recognized as a valuable strategy in promoting a circular economy.

CAR-macrophage: Breaking new ground in cellular immunotherapy.

Chimeric Antigen Receptor (CAR) technology has revolutionized cellular immunotherapy, particularly with the success of CAR-T cells in treating hematologic malignancies. However, CAR-T cells have the limited efficacy of against solid tumors. To address these limitations, CAR-macrophages (CAR-Ms) leverage the innate properties of macrophages with the specificity and potency of CAR technology, offering a novel and promising approach to cancer immunotherapy. Preclinical studies have shown that CAR-Ms can effectively target and destroy tumor cells, even within challenging microenvironments, by exhibiting direct cytotoxicity and enhancing the recruitment and activation of other immune cells. Additionally, the favorable safety profile of macrophages and their persistence within solid tumors position CAR-Ms as potentially safer and more durable therapeutic options compared to CAR-T cells. This review explores recent advancements in CAR-Ms technology, including engineering strategies to optimize their anti-tumor efficacy and preclinical evidence supporting their use. We also discuss the challenges and future directions in developing CAR-Ms therapies, emphasizing their potential to revolutionize cellular immunotherapy. By harnessing the unique properties of macrophages, CAR-Ms offer a groundbreaking approach to overcoming the current limitations of CAR-T cell therapies, paving the way for more effective and sustainable cancer treatments.

Spray-Deposited TiO2 Layers on Aluminum Foil for Sustainable Water Remediation

In this study, we developed TiO2-coated aluminum (TiO2/Al) surfaces using eco-friendly methods to create efficient and environmentally friendly photoactive materials with the potential to enhance water purification systems. TiO2 particles were deposited onto aluminum foil surfaces via a spray method, followed by heat treatment at 200 °C for 15 min. The morphology of the TiO2/Al surfaces, both before and after photocatalytic treatment, was characterized using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The photocatalytic properties of these modified surfaces were evaluated through the degradation of rhodamine B (RB), methylene blue (MB), and methyl orange (MO) under simulated solar and UV–LED irradiation. Among the dyes tested, MO exhibited the highest degradation, influenced by factors such as absorption maximum, molecular structure, charge, and the number of condensed rings. The computational study of interactions between dye molecules and the combined nanoparticle revealed that the binding was the strongest in the case of MO dye. This study also explored the influence of varying the number of TiO2/Al surfaces in solution (one, five, and ten) on the photodegradation efficiency. The solution with five TiO2/Al surfaces demonstrated optimal performance, achieving a 16% degradation of RB. The reusability of the TiO2/Al surfaces was confirmed through five successive runs of RB degradation. The results indicate that TiO2/Al surfaces are a promising solution for addressing water contamination challenges and advancing sustainable water treatment practices.

Enhancing membrane fouling control in wastewater treatment processes through artificial intelligence modeling: research progress and future perspectives

AbstractMembrane filtration processes have demonstrated remarkable effectiveness in wastewater treatment, achieving high contaminant removal and producing high-quality effluent suitable for safe reuse. Membrane technologies play a primary role in combating water scarcity and pollution challenges. However, the need for more effective strategies to mitigate membrane fouling remains a critical concern. Artificial intelligence (AI) modeling offers a promising solution by enabling accurate predictions of membrane fouling, thus supporting advanced fouling mitigation strategies.This review examines recent progress in the application of AI models, with a particular focus on artificial neural networks (ANNs), for simulating membrane fouling in wastewater treatment processes. It highlights the substantial potential of ANNs, particularly the widely studied multi-layer perceptron (MLP) and other emerging configurations, to accurately predict membrane fouling, thereby enhancing process optimization and fouling mitigation efforts. The review discusses both the potential benefits and current limitations of AI-based strategies, analyzing recent studies to offer valuable insights for designing ANNs capable of providing accurate fouling predictions. Specifically, it provides guidance on selecting appropriate model architectures, input/output variables, activation functions, and training algorithms. Finally, this review highlights the critical need to connect research findings with practical applications in full-scale wastewater treatment plants. Key steps crucial to address this challenge have been identified, emphasizing the potential of AI modeling to revolutionize process control and drive a paradigm shift toward more efficient and sustainable membrane-based wastewater treatment.

Evaluating the efficacy of palm waste in adsorption processes for wastewater treatment: A review

AbstractThe growing environmental concerns related to industrial effluents and waste underscore the urgent need for sustainable and cost‐effective wastewater treatment solutions. This review investigates the efficacy of palm waste‐derived adsorbents for removing heavy metals and organic pollutants from wastewater. It explores various modifications—including physical, chemical, and nanomaterial enhancements—applied to palm waste materials such as palm kernel shells, empty fruit bunches, and palm oil fuel ash, aimed at improving their adsorption capacities. The review reveals that these modified palm waste adsorbents demonstrate high removal efficiencies for contaminants like Cu(II), Pb(II), and organic dyes, often surpassing conventional adsorbents. Nonetheless, challenges remain, such as optimizing adsorbent preparation, understanding adsorption mechanisms in multi‐component systems, and enhancing adsorbent reusability. This review highlights the need for continued research to address these issues and advance the application of palm waste‐based materials in sustainable wastewater treatment.

Electrocatalytic arsenic removal: Unveiling selective capturing and conversion with a redox-active silica-lignosulfonate hybrid framework

Addressing the global challenge of arsenic groundwater pollution to ensure a safe water supply is crucial. Thus, we developed a versatile ferrocene (Fc) incorporated silica-lignosulphonate nano framework (Fc–Si–LS). This framework was precisely designed to target and transform the toxic arsenite (As+3) into a controllable form of arsenic (As+5). Results revealed that the unique Fc–Si–LS framework had significantly targeted As+3 and showed an impressive selective conversion (84 %) performance even at high concentrations (1 mM). Additionally, in real water application (As = 150 μg/L), the As+3 conversion rate remained effective (∼81.6 %). Remarkably, the synergy between Fc and Si–LS resulted in an exceptional adsorption capacity (106 mg/g) at 1.2 V, attaining a low energy consumption of only 0.072 kWh/m3. DFT simulations established a phenomenon that simultaneous selective capturing and conversion of arsenic requires a redox moiety integration on the catalyst surface to accept electrons from the selectively trapped As+3 to the electrode. Hence, this study highlighted the potential of precisely persuading Si–LS based redox-active nano frameworks in evolving energy effective solutions for arsenic removal from drinking water, thereby offering significant implications for sustainable water treatment technologies.

The role of TiO2 and gC3N4 bimetallic catalysts in boosting antibiotic resistance gene removal through photocatalyst assisted peroxone process

Antibiotics are extensively used in human medicine, aquaculture, and animal husbandry, leading to the release of antimicrobial resistance into the environment. This contributes to the rapid spread of antibiotic-resistant genes (ARGs), posing a significant threat to human health and aquatic ecosystems. Conventional wastewater treatment methods often fail to eliminate ARGs, prompting the adoption of advanced oxidation processes (AOPs) to address this growing risk. The study investigates the efficacy of visible light-driven photocatalytic systems utilizing two catalyst types (TiO2-Pd/Cu and g-C3N4-Pd/Cu), with a particular emphasis on their effectiveness in eliminating blaTEM, ermB, qnrS, tetM. intl1, 16 S rDNA and 23 S rDNA through photocatalytic ozonation and peroxone processes. Incorporating O3 into photocatalytic processes significantly enhances target removal efficiency, with the photocatalyst-assisted peroxone process emerging as the most effective AOP. The reemergence of targeted contaminants following treatment highlights the pivotal importance of AOPs and the meticulous selection of catalysts in ensuring sustained treatment efficacy. Furthermore, Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis (PCR-DGGE) analysis reveals challenges in eradicating GC-rich bacteria with TiO2 and g-C3N4 processes, while slight differences in Cu/Pd loadings suggest g-C3N4-based ozonation improved antibacterial effectiveness. Terminal Restriction Fragment Length Polymorphism analysis highlights the efficacy of the photocatalyst-assisted peroxone process in treating diverse samples.

Testing the effectiveness of a virtual sustained tobacco treatment: Initial reporting of findings from the EAQ171CD randomized clinical trial conducted by ECOG-ACRIN within the NCI Community Oncology Research Program (NCORP).

376 Background: Persistent smoking among patients diagnosed with cancer is associated with adverse clinical outcomes, yet clinical guidelines for tobacco use interventions have not been integrated into community oncology settings. We conducted a trial of a virtual sustained tobacco treatment intervention across community oncology settings nationally. Methods: This randomized clinical trial, conducted through ECOG-ACRIN, compared the effectiveness of sustained telehealth counseling plus medication (Virtual Sustained Treatment; VST) to referral to the NCI quitline (Enhanced Usual Care; EUC) in assisting recently diagnosed cancer patients to quit smoking. The VST group received up to 11 synchronous telehealth sessions (4 weekly, 4 biweekly, 3 monthly) of motivational counseling and up to 12-weeks of free NRT patch and/or lozenge. Eligibility criteria included adults within 4 months of a new cancer diagnosis, cigarette use in the past 30 days, English/Spanish speaking, and access to an internet-enabled device. The primary outcome is 6-month self-reported 7-day point prevalence abstinence. Results: From 08/2019 to 12/2022, 306 patients were randomized from 30 NCORP Community Sites and 7 Minority/Underserved NCORP sites. Participants were 70.9% female; 86.3% White; 8.8% Black; and 2.9% Hispanic; median age 57 years; 25.5% completed a college degree; 50.3% stages 0-2; 46.4% had non-smoking-related tumors. Median cigarettes per day was 12.0; 72.2% (n = 221/306) smoked within 30 minutes of waking; 49.0% (n = 150/306) were in precontemplation/contemplation stage of readiness to quit. 73.8% (222/301) and 72.2% (210/291) completed the 3 and 6-month outcome assessments. Classifying missing smoking status as smokers, 6-month abstinence rates were 28.4% (42/148) in the VST group vs. 14.7% (21/143) in the EUC group (p<.005). For secondary outcomes, there were no significant differences when adjusted for multiple comparisons (α = 0.0025); abstinence at 3-months was 24.7% (38/154) in the VST group vs. 15.0% (22/147) in the EUC group (p=.035); continuous abstinence at 6 months was 18.9% (28/148) in the VST vs 9.1% (13/143) in the EUC (p=.016). 80.8% (126/156) of individuals randomized to VST participated in counseling; of those, 59.5% (75/126) completed at least 6 sessions, 46.0% (58/126) completed at least one monthly booster session, and 85.7% (108/126) were dispensed 4 weeks of NRT. Conclusions: Among recently diagnosed cancer patients, sustained remotely delivered telehealth counseling and free NRT produced a significantly higher 6-month quit rate than a quitline referral. Findings support adopting a policy of widespread sustained tobacco treatment and implementation of tobacco treatment into community oncology care settings nationwide. Clinical trial information: NCT03808818 .

Bismuth oxyiodide-based composites for advanced visible-light activation of peroxymonosulfate in pharmaceutical mineralization

The presence of pharmaceutical pollutants in water bodies represents a significant environmental and public health concern, largely due to their inherent persistence and potential to induce antibiotic resistance. Advanced oxidation processes (AOPs) that employ peroxymonosulfate (PMS) activation have emerged as an effective means of degrading these contaminants. Bismuth oxyiodides (BiOI), which are known for their visible-light photocatalytic properties, demonstrate considerable potential for removal of pharmaceutical pollutants. This study examines the synthesis and performance of BiOI-based composites with barium ferrite (BFO) nanoparticles for enhanced PMS activation under visible light. BiOI and Bi5O7I were synthesized via solvothermal and electrodeposition methods, respectively, and their morphologies and crystalline structures were observed to exhibit distinctive characteristics following annealing. The formation of the composite with BFO resulted in an improvement in the catalytic properties, which in turn enhanced the surface area and availability of active sites. The objective of the photocatalytic studies was to evaluate the degradation and mineralization of tetracycline (TC) under visible light, PMS, and combined conditions. The Bi5O7I(ED)-BFO catalyst was identified as the optimal candidate, achieving up to 99.8% TC degradation and 99.4% mineralization within 90 min at room temperature. The synergistic effect of BFO in BiOI-based composites significantly enhanced performance across all conditions, indicating their potential for efficient remediation of pharmaceutical pollutant. The material's performance was further evaluated in tap water, where the degradation efficiency decreased to 56.4% and mineralization to 38.2%. These results reflect the challenges posed by complex water matrices. However, doubling the PMS concentration to 5 mM led to improved outcomes, with 93.8% degradation and 81.4% mineralization achieved. These findings demonstrate the material's robust potential for treating pharmaceutical pollutants in real-world conditions, advancing sustainable water treatment technologies.

Selective oxidation of electron-rich pollutants in peroxymonosulfate-activated electro-Fenton system: the role of microenvironment-regulated cathode

Electro-Fenton technologies driven by peroxymonosulfate (PMS) activation have been extensively explored for abatement of organic pollutants from water. Unfortunately, a great diversity of matrix components in contaminated water scenarios inevitably and significantly compromises the efficiency of the generated radicals toward target pollutants. Thus, selective oxidation of the electro-Fenton technologies is urgently desired for cost effective and sustainable water treatment, but challenged by the traditional electron transfer pathway from cathode to PMS to mainly form SO4•− and HO• radicals. In this study, we successfully realized selective generation of 1O2, a non-radical species specific for electron-rich pollutants, by regulating the second-shell coordination environment of single-atom Fe in carbonaceous cathode. The doped electron-accepting B drives directional electron transfer from PMS to electrode and inhibiting the undesirable radical pathways. Besides, the electrochemical reduction of H+ in-situ generated from the dissociation of H-O in PMS is favourable for the formation of 1O2 as high as 163.4 μmol.L−1min−1. Fast and preferential removal of sulfonamides pollutants in different water matrices demonstrated the excellent matrix tolerance of the newly developed electro-Fenton process. A pilot electrochemical device was designed to further selective remove phenols in real-scenario application. No residual phenol was detected (<0.01 mg/L) with TOC removal around 50% (down to 23.9±0.3 mg L−1) during the continuous 24-h operation. This study is also believed to shed new light on how to achieve desirable electrochemical reactions via microenvironmental regulation in response to sustainable water decontamination and beyond.

Bioremediation and microbiome-generating electricity in butter catfish (Ompok bimaculatus) aquaculture wastewater treatment via water fern (Azolla microphylla)

The increasing volume of wastewater from fish farming poses a serious environmental threat. This study investigated a novel treatment method for butter catfish (Ompok bimaculatus) wastewater using a constructed wetland-microbial fuel cell (CW-MFC) integrated with the water fern Azolla microphylla. The system was effectiveness in removing pollutants like electrical conductivity (EC), total dissolved solids (TDS), ammonium, nitrate, nitrite, and phosphate was evaluated. Additionally, the electricity generation capabilities were measured. The CW-MFC system achieved significant removal rates: 67.65% for EC, 61.67% for TDS, 100% for ammonium, 75.00% for nitrate, 81.25% for nitrite, and 70.00% for phosphate. Furthermore, the system generated a maximum open-circuit voltage (OCV) of 690±90 mV, a current density (CD) of 7.29±0.43 mA/m³and a power density (PD) of 0.37±0.04 mW/m³. Analysis of the microbial community revealed a diverse root consortium dominated by bacterial genera including Phreatobacter, Emticicia and Rhodobacter, along with fungal genera such as Strelitziana, Ramularia, Cladosporium,Trichomerium, Cercospora, Erythrobasidium and Fusarium. These findings suggest that CW-MFC systems integrated with A. microphylla offer a promising approach for sustainable and efficient treatment of wastewater from catfish farming while simultaneously generating bioelectricity.