Efficient Wastewater Treatment Research Articles

Synthesis and characterization of La-doped SnO2 nanoparticles with different shape: A comprehensive study on morphology, structure, and photocatalytic efficiency for eco-friendly wastewater treatment

New controllable synthetic approach to obtain of La-doped SnO2 nanoparticles based on the combination of co-precipitation method with post synthetical hydrothermal treatment has been developed. Nanoparticles with various shape (3 nm spheres and 5 nm cubes) and structural parameters, i.e. different amount of oxygen vacancies and defects, and different dopant concentrations of 11 mol% and 33 mol% were fully characterized using XRD, FTIR, XPS and Raman spectroscopy, TEM, SSA evaluation, optical absorption spectra study, luminescence spectroscopy, including quantum chemical calculations.It was shown that hydrothermal treatment (240 °C during 6 h) promotes nanoparticle growth via the mechanism of oriented attachment. Original computational approach based on the calculation of interaction energies between ions and crystal facets was engaged to study the growth process.The presence of intrinsic photoluminescence (406, 414, 438, 460, 500 and 676 nm) for all obtained samples was established, determined by a complex set of different parameters for sub-10 nm nanoparticles.Photocatalytic efficiency of 95 % on the example of methylene blue under commercially available LED lamp described via quantum chemical modelling and tested on the example of a colorless antibiotic solution. A clear dependance of the morphological and structural parameters on the photocatalytic properties has been obtained and studied in detail.Novel concept based on a combination of chemical and computational method, for effective visible-light driven photocatalyst synthesis with potential antibacterial properties for complex eco-friendly wastewater treatment was proposed.

Bacterial and microalgal co-fixation for remediation of industrial wastewater contaminated with arsenic, mercury, and other pollutants

Microbial remediation is an efficient approach for improving heavy metal-contaminated water environments. Herein, this article developed a composite bacterial agent (CBA) with a high heavy metal tolerance. Within 12 h, the CBA demonstrated removal efficiencies of 65.18 ± 1.53% for As and 60.73 ± 0.94% for Hg in wastewater. This study prepared bacterial–algal fixed spheres (BAFS) to further enhance the removal efficiencies of As and Hg. Moreover, during desorption using 0.1 mol/L HNO3 for 60 min, the BAFS maintained high removal efficiencies for As and Hg after five adsorption–desorption cycles. Applying BAFS to industrial wastewater collected from factory outfall caused substantial reductions in chemical pollutants and other heavy metals. Scanning electron microscopy analysis further revealed that the internal cavities formed through the crosslinking of immobilized materials provided excellent survival carriers for bacteria and microalgae. Infrared spectroscopy analysis demonstrated the involvement of three functional groups, namely -OH, -CH2-, and C-O-C, in pollutant adsorption. Additionally, microbial community diversity analysis indicated that immobilization effectively preserved the pollutant adsorption ability of the microorganisms, increasing the abundance of functional microbial populations. These characteristics improved the efficiency of industrial wastewater treatment while promoting recycling.

Hydrothermal synthesis of high crystallinity ZSM-5 zeolite from coal gasification coarse slag and mother liquor circulation for efficient coal chemical wastewater purification.

A hydrothermal synthesis method was developed to produce high crystallinity ZSM-5 zeolite using coal gasification coarse slag (CGCS) as the raw material. Instead of the expensive NaOH(s.), Na2SiO3(s.) was utilized to activate, depolymerize, and recombine Si and Al elements in the CGCS. The mother liquor circulation technology was employed to recover and reuse raw materials and residual reagents (Na2SiO3(aq.) and TPABr), reducing waste emissions and enhancing resource utilization efficiency. The synthesized ZSM-5 had a specific surface area of 455.675 m2g-1, pore volume of 0.284 cm3g-1, and pore diameter of 2.496nm. The influence of various factors on the morphology and crystallinity of ZSM-5 was investigated, resulting in the production of ZSM-5 with higher specific surface area and pore volume. Adsorption experiments showed that WU-ZSM-5 exhibited a removal efficiency of 85% for ammonia nitrogen (NH4+-N(aq.)), validating its effectiveness in coal chemical wastewater purification. The mother liquor recycling technology enabled zero-emission utilization of solid waste resources and improved the utilization rate of alkali and template to 90%. These results demonstrate the potential application of the developed method in the efficient treatment of coal chemical wastewater.

Optimization of on-site wastewater treatment efficiency and recovery based on nutrient mobility and adsorption kinetics modelling using HYDRUS-2D coupled with PHREEQC

A closed-loop on-site wastewater treatment system (OWT) was studied comprising steps of septic tank to remove organics (Biological Oxygen Demand (BOD)), biofiltration clarifier for biological removal of nitrogen (N), phosphorus (P) and BOD, reactive Polonite® filter for chemical adsorption and precipitation removal of dissolved P, and tidal flow constructed wetland (TFCW) sand filter for polishing the effluent to low P and N effluent Swedish standards. The field experimental data that have been used to optimize TFCW design in the numerical modelling using HYDRUS-2D coupled with and without PHREEQC indicated that the adsorption efficiency of the reactive Polonite® adsorbent was nearly double to that obtained in TFCW sand filters for PO4-P (95 %) and Total-P (85 %) removal in summer at a high temperature range (15.4–18.8 °C) and pH range (9.9–10.8). The weaker PO4-P (53 %) and Total-P (25 %) removal efficiency in winter was due to a low temperature (1.5–8.1 °C) and low pH (7.2–7.9). This decrease in pH was attributed to salinity in the domestic wastewater and dilution of rainwater. Modelling results revealed that the transport mechanisms and rate of P adsorption kinetics in the TFCW sand filters enhanced with calcium and iron flow from chemical dissolution in the preceding Polonite® adsorbent was increased with the increase in temperature. However, the P adsorption was less sensitive at high ferrihydrite (Fe(OH)3) dose, suggesting limited effects of cations dissolution and abundance of metal oxides and hydroxide ions at the mineral surface for anions exchange with phosphate for surface complexation. The strategy of combining field data and modelling provided valuable insights for assessing adaptability and optimizing TFCW design under variable fluxes and scenario effects of insulated/uninsulated and dilution by rainwater in cold-climate regions.

Electrochemical Hydrogen Peroxide Generation and Removal of Moxifloxacin by Electro-Fenton Process

In this study, the removal of moxifloxacin, an antibiotic of the fluoroquinolone group, from aqueous solutions was investigated using the electro-Fenton process. As the efficiency of the electro-Fenton process is highly dependent on the amount of H2O2 produced during process, the formation of H2O2 under acidic conditions was also investigated. In this context, the effects of applied current, cathode type and O2 flow rate on H2O2 production were investigated using boron-doped diamond anode. The highest H2O2 production was achieved using the boron-doped diamond anode and the graphite felt cathode. In addition, the optimum conditions for the applied current and oxygen flow rate for H2O2 production were determined to be 0.25 A and 0.1 L min−1, respectively. The effects of applied current and Fe2+ concentration in the electro-Fenton process on the removal of moxifloxacin were investigated. It was found that the moxifloxacin removal rate increased with increasing applied current. The highest H2O2 accumulation was observed at 0.25 A applied current, and moxifloxacin removal also reached 93.6% after 60 min. The moxifloxacin removal rate reached the highest value at Fe2+ concentration of 0.01 mM. This study provides promising results for the efficient treatment of moxifloxacin-containing wastewater by the electro-Fenton process without the addition of H2O2 using boron-doped diamond anode anode and graphite felt cathode.

A bio-based strategy for efficient industrial wastewater treatment using TiO2 photocatalysis

A bio-based strategy for efficient industrial wastewater treatment using TiO2 photocatalysis

Advanced microcrystalline nanocellulose-based nanofiltration membranes for the efficient treatment of wastewater contaminated with cationic dyes

Advanced microcrystalline nanocellulose-based nanofiltration membranes for the efficient treatment of wastewater contaminated with cationic dyes

Unlocking potential: Exploring the methane production potential in anaerobic co-digestion of cassava wastewater and glycerol

This study aimed at evaluating the feasibility of CH4 production in a mesophilic (30 °C) single-stage anaerobic co-digestion of cassava wastewater (CW) and glycerol in an anaerobic fluidized bed reactor (AFBR) with mixing ratio of 50 % / 50 % CW/Gly on a (chemical oxygen demand)COD basis. Thus, the following strategy was used: increasing the organic loading rate (OLR) (1–20 g COD.L−1.d−1) by increasing the substrate concentration (1–20 g COD.L−1) and applying a hydraulic detention time (HRT) of 24 h. The AFBR presented a maximum methane (CH4) content of 88.38±1.94 % and a CH4 yield (MY) of 293.48±18.37 mL of CH4.mL−1CODrem in the OLR of 1 g COD.L−1.d−1 and the maximum methane production rate (MPR) of 62.09±2.75 mL of CH4.L−1.h−1 in the OLR of 20 g COD.L−1.d−1. The conversion of glycerol and carbohydrates remained above 91±0.54 % and 82±2.79 %, respectively, and the COD conversion was above 80±0.65 %. The main metabolites were HAc, HPr, HBu, EtOH and HVa. The most abundant genera identified in the AFBR were Izemoplasmatales and Enterobacteriaceae for the bacteria domain, and Methanosaeta, Methanobacterium for the archaea domain. The single-stage system is robust and can operate with higher OLR without reducing the efficiency of wastewater treatment and CH4 production.

Utilizing banana peel in conjunction with TiO2 photocatalyst for the efficient decolorization of malachite green

Porous materials are frequently integrated into TiO2 photocatalysts due to their enhanced surface area and reaction efficiency. This study aimed to enhance the efficiency of wastewater treatment by developing a TiO2 combined with banana peel (BP) through the sol-gel method. The TiO2/BP composite was extensively analyzed using a range of methods, such as X-ray diffraction (XRD), field emission transmission electron microscopy (FESEM), energy dispersive X-ray (EDX) analysis, diffuse reflectance spectroscopy (DRS UV–vis), photoluminescence spectra (PL), and Brunauer–Emmett–Teller (BET) analysis. Subsequent evaluation of the photoactivity of the TiO2/BP composite compared to bare TiO2 particles revealed a noteworthy enhancement in decolorizing malachite green (MG) dye under visible light. Furthermore, recyclability testing further demonstrated consistent performance for up to four cycles, highlighting the potential application of this porous material-based photocatalytic composite in wastewater treatment.

Highly adsorptive removal of heavy metal, dye, and antibiotic pollutants using functionalized graphene nanosheets sono-electrochemically derived from graphitic waste

The development of highly adsorptive materials at low cost is critically important for efficient treatment of industrial wastewater. We herein report a one-step sonoelectrochemical strategy to synthesize functionalized graphene (FG) nanosheets as an effective adsorptive material using graphite waste from spent household batteries. Scanning/transmission electron and Raman microscopy studies reveal that the as-synthesized nanosheets are composed of few (2–6) graphene layers. Additionally, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses imply the presence of oxygen functional groups on the nanosheets (CO and -COOH, oxygen content of 4.29%), which are immensely beneficial for the electrostatic adsorption with heavy metals, dyes, and antibiotics in aqueous solutions. As expected, FG nanosheets exhibit potent capabilities of handling a wide range of pollutants, such as methylene blue, methyl orange, enrofloxacin, and Pb2+, with high adsorption performances (99.95% and 21.21 mg/g for Enrofloxacin, 98.93% and 119.3 mg/g for methylene blue, 95.82% and 25.67 mg/g for methyl orange, 95.56% and 86.10 mg/g for Pb2+). These findings therefore show a great promise for practical uses of the FG material as efficient adsorbents in eliminating metallic, organic, and antibiotic pollutants in water.

Fabrication of Loose Nanofiltration Membrane by Crosslinking TEMPO-Oxidized Cellulose Nanofibers for Effective Dye/Salt Separation.

Dye/salt separation has gained increasing attention in recent years, prompting the quest to find cost-effective and environmentally friendly raw materials for synthesizing high performance nanofiltration (NF) membrane for effective dye/salt separation. Herein, a high-performance loose-structured NF membrane was fabricated via a simple vacuum filtration method using a green nanomaterial, 2,2,6,6-tetramethylpiperidine-1-oxide radical (TEMPO)-oxidized cellulose nanofiber (TOCNF), by sequentially filtrating larger-sized and finer-sized TOCNFs on a microporous substrate, followed by crosslinking with trimesoyl chloride. The resulting TCM membrane possessed a separating layer composed entirely of pure TOCNF, eliminating the need for other polymer or nanomaterial additives. TCM membranes exhibit high performance and effective dye/salt selectivity. Scanning Electron Microscope (SEM) analysis shows that the TCM membrane with the Fine-TOCNF layer has a tight layered structure. Further characterizations via Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) confirmed the presence of functional groups and chemical bonds of the crosslinked membrane. Notably, the optimized TCM-5 membrane exhibits a rejection rate of over 99% for various dyes (Congo red and orange yellow) and 14.2% for NaCl, showcasing a potential candidate for efficient dye wastewater treatment.

A pilot-scale anoxic-anaerobic-anoxic-oxic combined with moving bed biofilm reactor system for advanced treatment of rural wastewater

Rural domestic poses a significant challenge to treatment technologies due to significant fluctuations in both water quality, particularly in terms of carbon concentration, and quantity. Conventional biological technology, such as anaerobic-anoxic-oxic (A2O) systems, is inefficient. In this work, a continuous pilot-scale anoxic-anaerobic-anoxic-oxic (A3O) reactor with a moving bed biofilm reactor (MBBR) system was constructed and optimized to improve the treatment efficiency of rural domestic wastewater. The sludge return ratio, volume ratio of the oxic-to-anoxic zone (Voxi/Vano), step-feeding and hydraulic retention time (HRT) at low temperature were considered the main parameters for optimization. Microbial analysis was performed on both the mixed liquor and carrier of the A3O-MBBR system under initial and post-optimized conditions. The results indicated that the A3O-MBBR improved the treatment efficiency of rural domestic wastewater, especially for total phosphorus (TP), which increased by 20 % compared with that of the A2O-MBR. In addition, the removal efficiencies of nitrogen and phosphorus were further optimized, and the average concentrations of total nitrogen (TN) and TP in the effluent reached 2.46 and 0.364 mg/L, respectively, at a sludge reflux ratio of 100 or 150 %, Voxi/Vano =200 %, step-feeding of 0.5Q/0.5Q (anaerobic/anoxic) and HRT of 15 h at low temperature in the A3O-MBBR, which met standard A of GB18918–2002, China (TN < 15 mg/L, TP < 0.5 mg/L). The average rate of attaining the standard increased by 58.63 % (post optimization). The microbial analysis showed an increase in species diversity and richness after the parameters were optimized. Moreover, compared to the microbial community structure before optimization, the post-optimization exhibited a more stable microbial structure with a significant enrichment of functional bacteria. Defluviimonas, Novosphingobium and Bifidobacterium, considered as the dominant nitrification or denitrifying bacteria, were enriched in the suspended sludge of the MBBR reactor, which the relative abundance increased by 3.11 %, 3.84 %, and 3.24 %, respectively. Further analysis of the microbial community in the carrier revealed that the abundance of Nitrospira and the denitrifying bacteria carried by the carrier were much greater than those in the suspended sludge. Consequently, the microorganism cooperation between suspended sludge and biofilm might be responsible for the improved performance of the optimized A3O-MBBR.

Catalytic degradation of BPA by bamboo leaf-derived KOH-activated porous biocarbon loaded with CoFe2O4-activated peroxymonosulfate

Multiphase catalysts with wide pH, high environmental adaptability, and high activity are urgently needed for the water's contaminants to break down. In this study, the biomass waste bamboo leaves were used as the carbon source and activated by KOH to further increase the active sites (the adsorption capacity was 8.06 times that of the unactivated material) loaded with cobalt ferrite composite catalyst CoFe2O4@PBCX, which could effectively activate the PMS to realize the degradation of BPA. The CoFe2O4@PBCX + PMS system demonstrated remarkable BPA degradation across a broad starting pH range (3–11), and 100% BPA removal was achieved in 9 min at pH=11. CoFe2O4@PBCX achieved excellent BPA removal performance under high salinity conditions (200 mM). The toxicity of BPA and its oxidation intermediates was predicted by the ECOSAR model, which proved that BPA was eventually degraded into non-toxic products. In the bisphenol A degradation device, no catalyst deactivation was observed after 14 h, and 80% removal was maintained after 40 h. This study showed that the synthesized CoFe2O4@PBCX is a highly efficient PMS activation catalyst, which has the potential of low cost, high efficiency, and ecological friendliness in practical wastewater treatment.

Molecular Simulation Studies of Pharmaceutical Pollutant Removal (Rosuvastatin and Simvastatin) Using Novel Modified-MOF Nanostructures (UIO-66, UIO-66/Chitosan, and UIO-66/Oxidized Chitosan).

The ubiquitous presence of pharmaceutical pollutants in the environment significantly threatens human health and aquatic ecosystems. Conventional wastewater treatment processes often fall short of effectively removing these emerging contaminants. Therefore, the development of high-performance adsorbents is crucial for environmental remediation. This research utilizes molecular simulation to explore the potential of novel modified metal-organic frameworks (MOFs) in pharmaceutical pollutant removal, paving the way for the design of efficient wastewater treatment strategies. Utilizing UIO-66, a robust MOF, as the base material, we developed UIO-66 functionalized with chitosan (CHI) and oxidized chitosan (OCHI). These modified MOFs' physical and chemical properties were first investigated through various characterization techniques. Subsequently, molecular dynamics simulation (MDS) and Monte Carlo simulation (MCS) were employed to elucidate the adsorption mechanisms of rosuvastatin (ROSU) and simvastatin (SIMV), two prevalent pharmaceutical pollutants, onto these nanostructures. MCS calculations demonstrated a significant enhancement in the adsorption energy by incorporating CHI and OCHI into UIO-66. This increased ROSU from -14,522 to -16,459 kcal/mol and SIMV from -17,652 to -21,207 kcal/mol. Moreover, MDS reveals ROSU rejection rates in neat UIO-66 to be at 40%, rising to 60 and 70% with CHI and OCHI. Accumulation rates increase from 4 Å in UIO-66 to 6 and 9 Å in UIO-CHI and UIO-OCHI. Concentration analysis shows SIMV rejection surges from 50 to 90%, with accumulation rates increasing from 6 to 11 Å with CHI and OCHI in UIO-66. Functionalizing UIO-66 with CHI and OCHI significantly enhanced the adsorption capacity and selectivity for ROSU and SIMV. Abundant hydroxyl and amino groups facilitated strong interactions, improving performance over that of unmodified UIO-66. Surface functionalization plays a vital role in customizing the MOFs for pharmaceutical pollutant removal. These insights guide next-gen adsorbent development, offering high efficiency and selectivity for wastewater treatment.

Preparation of Heterogeneous Fenton Catalysts Cu-Doped MnO2 for Enhanced Degradation of Dyes in Wastewater.

Herein, a series of heterogeneous Fenton catalysts, Cu doped MnO2 (CDM), with different Cu/Mn molar ratios were prepared via a hydrothermal reaction. Meanwhile, detailed characterizations were used to study the structures of CDM, and it is amazing that the morphology of CDM changed from nanowires to nanoflowers with an increasing amount of Cu doped. Apart from this, both the specific surface area and oxygen vacancy increased obviously with the increasing Cu/Mn molar ratio. Then, the degradation of different dyes was utilized to evaluate the catalytic activity of different CDM with H2O2 used as the oxidizing agent, and the 50%-CDM with the highest content of Cu doped displayed the best catalytic activity. Herein, the degradation efficiency (D%) of Congo red (CR) solution with low concentration (60 mg/L) reached 100% in 3 min, while the D% of CR solution with a high concentration (300 mg/L) reached 99.4% after 5 min with a higher dosage of H2O2. Additionally, the 50%-CDM also displayed excellent reusability, for which the D% values were still higher than 90% after the 14th cycles. Based on the structure characteristics and mechanism analysis, the excellent catalytic capacity of 50%-CDM was due to the combined influence of large specific surface area and abundant oxygen vacancy. Thus, a promising heterogeneous Fenton catalyst was developed in this study, which proved the treatment efficiency of actual dye wastewater.

Development and testing of alginate/C3N4porphyrin bead as a self-initiated Fenton photocatalyst for highly efficient atrazine removal

Fenton reaction has been widely used for efficient treatment of organic wastewater. However, its applications are limited by such key factors as pH < 3. In this study, we developed, tested, and optimized an alginate/C3N4porphyrin bead (C3N4por-SA) as a recyclable photocatalyst in a photocatalysis-self-Fenton process to overcome these limitations. Porphyrin-modified C3N4 (C3N4por) was used as the H2O2 donator, while Fe(III) nodes served as the Fenton reagent. The as-prepared floating alginate/C3N4por bead utilized the light source as a driving force for the catalysis. Under visible light irradiation for 6 h, the model pollutant atrazine was degraded by 70.96 % by the optimized photocatalyst (named as C3N4por-SA-Fe1Ca5), demonstrating better photocatalytic performance than alginate/C3N4 beads. This improvement was attributed to the higher H2O2 yield from C3N4por. The alginate/C3N4por bead showed better photocatalytic activity even after several consecutive cycles and could easily be recovered for reuse. Furthermore, Fe(III)/Ca(II) bimetallic alginate bead exhibited better photocatalytic activity and a higher content of •OH radicals than the Ca(II) monometallic alginate beads, due to the ability of Fe(III) nodes to serve as a Fenton reagent. The influences of light sources, and commonly existing matters (namely SO42−, Cl−, CO32−, NO3−, and humic acid) were investigated. Moreover, the alginate/C3N4por bead demonstrated good photocatalytic performance in a simulated natural environment without the addition of extra H2O2, with an atrazine removal percentage of up to 96.3 % after 3-h irradiation. These findings indicated the great potential of alginate/C3N4por bead in practical applications.

Study on Preparation of Calcium-Based Modified Coal Gangue and Its Adsorption Dye Characteristics.

Efficient and thorough treatment of dye wastewater is essential to achieve ecological harmony. In this study, a new type of calcium-based modified coal gangue (Ca-CG) was prepared by using solid waste coal gangue as raw material and a CaCl2 modifier, which was used for the removal of malachite green, methylene blue, crystal violet, methyl violet and other dyes in water. When the dosage of Ca-CG was 1-5 g/L, the dosage of Ca-CG was the main factor affecting the dye adsorption effect. The adsorption effects of Ca-CG on four dyes were as follows: malachite green > crystal violet > methylene blue > methyl violet. Kinetics, isotherms and thermodynamic analysis showed that the adsorption of malachite green, methyl blue, crystal violet and methyl violet by Ca-CG fitted the second-order kinetic model, and adsorption with chemical reaction is the main process. The adsorption of four dyes by Ca-CG conformed to the Freundlich model, which is dominated by multi-molecular layer adsorption, and the adsorption was easy to carry out. The adsorption process of Ca-CG on the four dyes was spontaneous. The results of FTIR, XRD and SEM showed that the calcium-based materials such as lipscombite and dolomite were the key to the adsorption of malachite green by Ca-CG, and the main mechanisms for the adsorption of malachite green by Ca-CG are surface precipitation, electrostatic action, and chelation reaction. Ca-CG adsorption has great potential for the removal of dye wastewater.

Emerging trends of ferrite-based nanomaterials as photocatalysts for environmental remediation: A review and synthetic perspective

Efficient wastewater treatment processes are in high demand for removing organic and inorganic pollutants. Photocatalysis, as an environmentally friendly technology, has shown significant progress in the treatment of contaminated wastewater. This review explores the potential of spinel ferrite-based nanomaterials as efficient photocatalysts for wastewater treatment. To enhance their properties, ferrites have been combined with advanced materials, such as BiOX, MXene, and g-C3N4 to form binary and ternary nanocomposites. We highlight the state-of-the-art in these binary and ternary spinel ferrite nanocomposites in the photocatalytic degradation of organic pollutants. These ferrite nanocomposites showed superior photocatalytic performance due to enhanced properties such as increasing the capacity for light utilization, slowing electron-hole recombination, and reducing agglomeration. Furthermore, our review explores recent research on template-assisted synthesis, a novel approach for fine-tuning the morphology of spinel ferrites and enhancing their catalytic efficiency. The impact of both the soft and hard templates on the properties of the produced ferrite nanomaterials is discussed. Overall, this unique combination of advanced nanocomposite materials and structural control using template-assisted approaches paves the way for a new generation of highly efficient photocatalysts. Thus, we provide a comprehensive overview of recent advances in the development of ferrite nanocomposites, underlining their potential as photocatalysts for environmental remediation applications.

A Study of the Feasibility of Pinus patula Biochar: The Regeneration of the Indigo Carmine-Loaded Biochar and its Efficiency for Real Textile Wastewater Treatment

The feasibility of an adsorbent material like biochar (BC) depends on its regeneration capacity and its ability to achieve high removal efficiencies on real wastewater (WW) effluents. In this study, the regeneration capacity of the Pinus patula BC previously used in the removal of Indigo Carmine from water was evaluated. The regeneration technique that resulted in the highest desorption efficiency was a thermo-chemical method that consisted of heating the spent BC in a stove at 160 °C for 45 min followed by regeneration with ethanol (C2H6O) at a concentration of 75% for 6 h. Through this regeneration method, it was found that Pinus patula BC could be used in seven consecutive adsorption–desorption cycles. The feasibility of this BC was also assessed by evaluating the adsorbent’s efficiency in real textile WW. Under optimal operational conditions (solution pH = 3, BC dose = 13.5 g/L, and BC particle size = 300–450 µm), the highest removal efficiencies in terms of colour and dissolved organic carbon (DOC) were 81.3 and 76.8%, respectively, for 120 min of treatment. The results obtained in the regeneration studies and the treatment of real textile WW suggested that the use of Pinus patula BC could be suitable to be scaled to an industrial level, contributing to sustainable development and the circular bioeconomy by using a waste to solve the dye pollution problem of another waste.

Unlocking the superior flexibility and enhanced catalytic oxidation performance of CoTiO3 nanofibrous membranes through zirconium doping

The development of continuous CoTiO3 (CTO) fibers with prominent catalytic oxidation activity, tunable fibrous structures, and improved recyclability is appealing for application in efficient organic wastewater treatment; however, inescapable flaws remain, such as their inherent brittleness and adverse operability. Herein, a facile and effective strategy is proposed for the fabrication of flexible and mechanically robust CTO nanofibrous membranes through a combination of element doping and sol–gel-assisted electrospinning. Compared with pristine CTO fibers, the resulting zirconium-doped CoTiO3 (ZCTO) nanofibrous membranes displayed remarkably enhanced flexibility and tensile mechanics, which were attributed to their lower crystallinity, smaller grain size, and fewer fiber surface defects. The developed ZCTO fibrous membrane demonstrated exceptional resistance to bending fatigue, retaining a polymer-like bending rigidity of approximately 25 mN even after undergoing 200 reciprocating bending cycles. Furthermore, the incorporation of zirconium into CTO clearly had an advantageous effect on the formation of oxygen vacancies, thereby enhancing the surface adsorption of peroxymonosulfate (PMS), accelerating the electron transfer process, and weakening the peroxy bonds. The tetracycline degradation efficiency of the ZCTO fibers remained at 81.4% within 10 min after 5 continuous cycles. Benefiting from their robust mechanical properties and excellent catalytic activity, the fabricated membranes demonstrated outstanding dynamic catalytic performance under gravity-driven conditions. More importantly, the reported strategy might be adopted and extended to develop a wide range of ceramic fibers with enhanced flexibility and mechanics for catalytic oxidation.