Genome and pan-genome analysis of a new exopolysaccharide-producing bacterium Pyschrobacillus sp. isolated from iron ores deposit and insights into iron uptake.

Bacterial exopolysaccharides (EPS) have emerged as one of the key players in the field of heavy metal-contaminated environmental bioremediation. This study aimed to characterize and evaluate the metal biosorption potential of EPS produced by a novel Psychrobacillus strain, NEAU-3TGS, isolated from an iron ore deposit at Tamra iron mine, northern Tunisia. Genomic and pan-genomic analysis of NEAU-3TGS bacterium with nine validated published Psychrobacillus species was also performed. The results showed that the NEAU-3TGS genome (4.48 Mb) had a mean GC content of 36%, 4,243 coding sequences and 14 RNA genes. Phylogenomic analysis and calculation of nucleotide identity (ANI) values (less than 95% for new species with all strains) confirmed that NEAU-3TGS represents a potential new species. Pangenomic analysis revealed that Psychrobacillus genomic diversity represents an "open" pangenome model with 33,091 homologous genes, including 65 core, 3,738 shell, and 29,288 cloud genes. Structural EPS characterization by attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy showed uronic acid and α-1,4-glycosidic bonds as dominant components of the EPS. X-ray diffraction (XRD) analysis revealed the presence of chitin, chitosan, and calcite CaCO3 and confirmed the amorphous nature of the EPS. Heavy metal bioabsorption assessment showed that iron and lead were more adsorbed than copper and cadmium. Notably, the optimum activity was observed at 37°C, pH=7 and after 3 h contact of EPS with each metal. Genomic insights on iron acquisition and metabolism in Psychrobacillus sp. NEAU-3TGS suggested that no genes involved in siderophore biosynthesis were found, and only the gene cluster FeuABCD and trilactone hydrolase genes involved in the uptake of siderophores, iron transporter and exporter are present. Molecular modelling and docking of FeuA (protein peptidoglycan siderophore-binding protein) and siderophores ferrienterobactine [Fe+3 (ENT)]-3 and ferribacillibactine [Fe+3 (BB)]-3 ligand revealed that [Fe+3 (ENT)]-3 binds to Phe122, Lys127, Ile100, Gln314, Arg215, Arg217, and Gln252. Almost the same for [Fe+3 (ENT)]-3 in addition to Cys222 and Tyr229, but not Ile100.To the best of our knowledge, this is the first report on the characterization of EPS and the adsorption of heavy metals by Psychrobacillus species. The heavy metal removal capabilities may be advantageous for using these organisms in metal remediation.

Tailoring the characteristics of polyacrylonitrile nanofiltration membranes for nickel removal from wastewater: The influence of binary solvents and pore-forming agents.

This work presents the results of an investigation on the physiochemical and structural characteristics of polyacrylonitrile (PAN) nanofiltration (NF) membranes prepared using a novel concept of binary solvents for nickel (Ni) removal from wastewater streams. The thermodynamic and kinetic aspects are emphasized aiming to optimize dope formulation, membrane performance, and durability. The fabricated membranes were characterized by scanning electron microscopy (SEM), porosimetry, tensile stress/strain, and flux and rejection. Results revealed that the use of an equal (1:1) mixture of n-methyl-2-pyrrolidone (NMP) and dimethylformamide (DMF) as dope solvents led to the formation of membranes with enhanced performance, offering pure water flux of 2.33 L·m-2·h-1·bar-1 and Ni rejection of 90.84%. Moreover, the incorporation of 0.5 wt.% PEG as a pore-forming agent to the dope solution further boosted pure water flux to 4.97 L·m-2·h-1·bar-1 with negligible impact on Ni rejection. Besides attractive performance, the adopted strategy offered membranes of exceptionally high flexibility with no sign of defect or failure especially during module fabrication and testing enabling smooth and hassle-free scale-up and extension to other applications. PRACTITIONER POINTS: Optimized solvent mixture: A 1:1 blend of n-methyl-2-pyrrolidone (NMP) and dimethylformamide (DMF) as solvents resulted in enhanced membrane performance. High flux and Ni rejection: The fabricated membranes exhibited a pure water flux of 2.33 L·m-2·h-1·bar-1 and a remarkable Ni rejection of 90.84%. PEG enhancement: Incorporating 0.5 wt.% PEG as a pore-forming agent further improved the membrane's pure water flux to 4.97 L·m-2·h-1·bar-1, without compromising Ni rejection. Exceptional flexibility: The adopted strategy yielded membranes with exceptional flexibility, making them suitable for scale-ups and other applications.

Mechanochemical Thioglycolate Modification of Microscale Zero-Valent Iron for Superior Heavy Metal Removal.

Microscale zero-valent iron (mZVI) is widely used for water pollutant control and environmental remediation, yet its reactivity is still constrained by the inert oxide shell. Herein, we demonstrate that mechanochemical thioglycolate (TG) modification can dramatically enhance heavy metal (NiII, CrVI, CdII, PbII, HgII, and SbIII) removal rates of mZVI by times of 16.7 to 88.0. Compared with conventional impregnation (wet chemical process), this dry mechanochemical process could construct more robust covalent bonding between TG and the inert oxide shell of mZVI through its electron-withdrawing carboxylate group to accelerate the electron release from the iron core, and more effectively strengthen the surface heavy metal adsorption through metal(d)-sulfur(p) orbital hybridization between its thiol group and heavy metal ions. Impressively, this mechanochemically TG-modified mZVI exhibited an unprecedented NiII removal capacity of 580.4 mg Ni g-1 Fe, 17.1 and 9.5 times those of mZVI and wet chemically TG-modified mZVI, respectively. Its application potential was further validated by more than 10 days of stable groundwater NiII removal in a column flow reactor. This study offers a promising strategy to enhance the reactivity of mZVI, and also emphasizes the importance of the modification strategy in optimizing its performance for environmental applications.

Multifunctional engineering of Mangifera indica L. peel extract-modified bacterial cellulose hydrogel: Unveiling novel strategies for enhanced heavy metal sequestration and cytotoxicity evaluation.

The escalating interest in bacterial cellulose (BC) confronts a substantial obstacle due to its biologically inert properties. Hence, BC was modified with ethanolic mango peel extract (EEMP) for various industrial and medical applications of the novel nanocomposite (BC/EEMP). High-performance liquid chromatography (HPLC) delineated the phenolic composition of EEMP, revealing a repertoire of polyphenolic compounds, notably chlorogenic acid, gallic acid, catechin, and ellagic acid. EEMP exhibited broad-spectrum antimicrobial activity against Candida albicans and Staphylococcus aureus, with MIC of 0.018 mg/mL and 0.009 mg/mL, respectively. The removal mechanism of Pb2+ and Ni2+ by BC/EEMP nanocomposite membrane via SEM, EDX, FT-IR, and XRD was characterized, indicating deposition and aggregation of heavy metals with diminished porosity. Heavy metal removal optimization using the Box-Behnken design achieved maximal removal of 95.5 % and 90 % for Pb2+ and Ni2+, respectively. Moreover, BC/EEMP nanocomposite demonstrated selective dose-dependent anticancer activity toward hepatoma (HepG-2, IC50 of 208.8 µg/mL), skin carcinoma (A431, IC50 of 216.7 µg/mL), and breast carcinoma (MDA, IC50 of 197.5 µg/mL), attributed to the enhanced availability of biologically active polyphenolic compounds and physical characteristics of BC. This study underscores the remarkable potential of BC/EEMP nanocomposite for multifaceted industrial and biomedical applications, marking a pioneering contribution to the field.

Porous sodium alginate/cellulose nanofiber composite hydrogel microspheres for heavy metal removal in wastewater.

High adsorption capacity, high adsorption rate and reusable adsorbents are urgent needed for removing heavy metals from wastewater. In this study, porous sodium alginate/cellulose nanofiber (SA/CNF) composite hydrogel microspheres were prepared by combining sodium alginate with cellulose nanofibers by microfluidics technology and adding polyethylene glycol (PEG) as pore making agent. The SA/CNF composite hydrogel microspheres could efficiently adsorb heavy metals (Pb2+, Cu2+ and Cd2+) in wastewater. The influencing factors of adsorption process, including pH, temperature, initial concentration, coexisting ions and aquatic environments, were systematically discussed. The adsorption process was more consistent with Langmuir isotherm model and pseudo-second-order model in batch system, indicating the adsorption process was mainly chemical adsorption. The adsorption capacity to Pb2+ obtained by Langmuir model was as high as 544.66 mg/g at 20 °C. Fixed-bed column adsorption experiments demonstrated the excellent performance of the as-prepared SA/CNF microspheres for treatment of the flowing wastewater in a column system. Overall, a highly practical adsorption process based on hydrogel adsorbents was developed for the removal of heavy metals from actual wastewater.

Copper Ion Removal by Adsorption Using Fly Ash-Based Geopolymers: Process Optimization Insights from Taguchi and ANOVA Statistical Methods.

The present study aimed to use geopolymer materials synthesized from different fly ashes, which are promising for the adsorption of copper ions from aqueous solutions. The characterization of fly ashes and prepared adsorbents was performed by energy-dispersive X-ray spectroscopy (EDS) analysis, Brunauer-Emmett-Teller (BET) surface area analysis, and Scanning Electron Microscopy (SEM). Taguchi and ANOVA methods were used to predict the effect of different working parameters on copper ion removal by prepared geopolymers. Based on data obtained by the Taguchi method, it was found that the factor most influencing the adsorption process is the type of adsorbent used, followed by the solution pH, the reaction time, the adsorbent dose, and the initial copper ion concentration. The ANOVA results agree with the Taguchi method. The optimal conditions of the adsorption process were: fly ash C modified by direct activation with 2 M NaOH, at 70 °C for 4 h, solution pH of 5, initial pollutant concentration of 300 mg/L, 40 g/L adsorbent dose, and 120 min of reaction time. Copper ion removal efficiency was determined experimentally under optimal conditions, achieving a value of 99.71%.

Development of a continuous electrochemical reactor incorporated with waste-derived activated carbon electrode for the effective removal of hexavalent chromium from industrial effluent.

Being a recognized carcinogen, hexavalent chromium is hazardous to both human and environmental health. Thus, it is imperative to regulate and oversee their levels in a variety of industries, including textiles, dyes, pigments, and metal finishing. This study strives to reduce Cr(VI) in wastewater by using capacitive deionization in conjunction with an activated carbon-based electrode and a continuous electrochemical reactor (CER). Activated carbon derived from rubberwood sawdust demonstrated excellent properties, including a high surface area of 1157 m2 g-1. The electrical conductivity and mechanical stability of the electrode were enhanced by the incorporation of synthesized expanded graphite (EG) into the AC. Key parameters were optimized via systematic batch electroreduction experiments with an optimal response surface design. The efficacy of the fabricated CER was proved when it successfully reduced Cr(VI) in a 5 mg L-1 solution within 15 min under optimized conditions, in contrast to the considerably longer durations anticipated by conventional methods. Validation of these findings was done by treating industrial wastewater of 30 mg L-1 in the CER. The electroreduction of Cr(VI) followed the Langmuir isotherm with a maximum capacity of 13.491 mg g-1 and pseudo-second-order kinetics. These results indicate that the combined use of the modified AC electrode and CER holds potential as a sustainable and economical approach to effectively eliminate Cr(VI) from wastewater.

Scenedesmus sp. as a phycoremediation agent for heavy metal removal from landfill leachate in a comparative study: batch, continuous, and membrane bioreactor (MBR).

Improper disposal of municipal solid waste led to the release of heavy metals into the environment through leachate accumulation, causing a range of health and environmental problems. Phycoremediation, using microalgae to remove heavy metals from contaminated water, was investigated as a promising alternative to traditional remediation methods. This study explored the potential of Scenedesmus sp. as a phycoremediation agent for heavy metal removal from landfill leachate. The study was conducted in batch, continuous, and membrane bioreactor (MBR). In the batch system, Scenedesmus sp. was added to the leachate and incubated for 15 days before the biomass was separated from the suspension. In the continuous system, Scenedesmus sp. was cultured in a flow-through system, and the leachate was continuously fed into the system with flow rates measured at 120, 150, and 180 mL/h for 27 days. The MBR system was similar to the continuous system, but it incorporated a membrane filtration step to remove suspended solids from the treated water. The peristaltic pump was calibrated to operate at five different flow rates: 0.24 L/h, 0.30 L/h, 0.36 L/h, 0.42 L/h, and 0.48 L/h for the MBR system and ran for 24 h. The results showed that Scenedesmus sp. was effective in removing heavy metals such as lead (Pb), cobalt (Co), chromium (Cr), nickel (Ni), and zinc (Zn) from landfill leachate in all three systems. The highest removal efficiency was observed for Ni, with a removal of 0.083 mg/L in the MBR and 0.068 mg/L in batch mode. The lowest removal efficiency was observed for Zn, with a removal of 0.032 mg/L in the MBR, 0.027 mg/L in continuous mode, and 0.022 mg/L in batch mode. The findings depicted that the adsorption capacity varied among the studied metal ions, with the highest capacity observed for Ni (II) and the lowest for Zn (II), reflecting differences in metal speciation, surface charge interactions, and affinity for the adsorbent material. These factors influenced the adsorption process and resulted in varying adsorption capacities for different metal ions. The study also evaluated the biomass growth of Scenedesmus sp. and found that it was significantly influenced by the initial metal concentration in the leachate. The results of this study suggest that Scenedesmus sp. can be used as an effective phycoremediation agent for removing heavy metals from landfill leachate.

Chitosan-blended membranes for heavy metal removal from aqueous systems: A review of synthesis, separation mechanism, and performance.

The environmental pollution caused by heavy metal ions has become a serious global environmental issue. Heavy metal contaminants released from industrial effluents, agricultural runoff, and human activities, can enter into water resources. The toxicity of these heavy metal ions even at trace concentrations presents a substantial hazard to both aquatic systems and human well-being. The membrane separation processes have become more promising sustainable techniques for the separation of metal ions from the effluent. The research efforts have been concentrated on improving the synthesis of membranes and membrane materials to facilitate the sustainable separation of heavy metals. The application of chitosan in the fabrication of membranes is getting more attention. Chitosan, a natural polysaccharide derived from chitin, is abundant in nature and has active hydroxyl and amino groups suitable for the separation of heavy metal ions. It exhibits excellent chelating tendency, biocompatibility, and biodegradability. The functionalization of chitosan to improve its mechanical strength, chemical stability, and antifouling properties has become an ongoing area of research. This review examines the synthesis and efficient applications of chitosan blended membranes. The review concludes by outlining the current challenges and proposing future research prospects to enhance the applicability of chitosan-blended membranes in environmental remediation.

Simulation of hexavalent chromium removal by electrocoagulation using iron anode in flow-through reactor.

An electrocoagulation (EC) model is developed for hexavalent chromium reduction and precipitation, using iron electrodes. Parallel removal mechanisms such as adsorption of chromium on ferrihydrite and direct reduction at the cathode is assumed negligible due to low concentration of Cr(VI). The reaction model presented for batch system represents species complexation, precipitation/dissolution, acid/base, and oxidation-reduction reactions. Batch reactor simulation is verified using experimental data obtained by Sarahney et al. (2012), where the effect of initial chromium concentration, pH, volumetric current density, and ionic strength is considered (Sarahney et al., 2012). The model couples multicomponent ionic transport in MATLAB with chemical reaction model in PHREEQC, as a widely used computational programming tool and a geochemical reaction simulator with comprehensive geochemistry databases. The suggested current density is 0.05-0.3mA/cm2 and the surface to volume ratio in batch reactor is considered 0.017 1/cm. Design parameters are presented for operation of a flow-through hexavalent chromium removal using electrocoagulation by iron electrode to treat Cr(VI) in range of 10-50 mg/L. The operational parameters for a flow-through EC reactor for Cr(VI) removal is suggested to follow [Formula: see text] .

Sulfhydryl functionalized two-dimensional Ti3C2Tx MXene for efficient removal of Hg2+ in water samples.

This study describes an adsorption method for the removal of Hg2+ from aquatic environments using sulfhydryl-functionalized Ti3C2Tx (SH-Ti3C2Tx). SH-Ti3C2Tx materials were synthesized through covalent interactions between dithiothreitol and two-dimensional Ti3C2Tx. The insertion of -SH groups increased the interlayer spacing of Ti3C2Tx, resulting in a 3-fold increase in the specific surface area of SH-Ti3C2Tx compared with the original Ti3C2Tx. The maximum Hg2+ adsorption capacity of SH-Ti3C2Tx was 3042 mg/g, which was 2.3-fold greater than that of Ti3C2Tx. After Hg2+ adsorption, SH-Ti3C2Tx was regenerated for repeated used by rinsing with HCl-thiourea. Next, SH-Ti3C2Tx was loaded onto a melamine sponge to construct SH-Ti3C2Tx adsorption columns suitable for continuous flow Hg2+ removal with extremely low flow resistance. Hg2+ removal rates exceeded 95 % when treating both high and low-concentration solutions (20 mg/L Hg2+ and 10 µg/L Hg2+). This study demonstrates the excellent adsorption-regeneration performance of SH-Ti3C2Tx, which has broad application prospects for the in-situ treatment of water contaminated with Hg2+.

Effective adsorptive removal of Pb2+ ions from aqueous solution using functionalized agri-waste biosorbent: New green mediation via Seidlitzia rosmarinus extract.

Currently, the use of natural adsorbent for the elimination of pollutants, such as heavy metals, from water has been extensively investigated. However, the low adsorption capacity of these natural adsorbents has led researchers towards the use of synthetic surfactants, which themselves can become environmental pollutants. In this research, an investigation was conducted to examine the impact of a surfactant obtained from the Seidlitzia rosmarinus plant on the adsorption properties of Pumpkin seed shell (PSS), a natural adsorbent. As a result, a modified version of PSS, known as functionalized Pumpkin seed shell (FPSS), was developed, and the effect of these two adsorbents on the elimination of Pb2+ has been investigated. FESEM, EDS, FTIR, and BET analyses were conducted to get detailed information of the adsorbent. Additionally, the effects of contact time, dosage of the adsorbent, pH of the solution, and temperature on the adsorbent were studied. The experimental data was fitted using Langmuir, Freundlich, Temkin, and Jovanovic isotherms. The PSS adsorbent was fitted best with the Langmuir isotherm, showing an adsorption capacity of 160.80 mg g-1, while the FPSS adsorbent was fitted with the Jovanovic isotherm, exhibiting an adsorption capacity of 553.57 mg g-1. Furthermore, kinetic modeling results indicated that the data for these adsorbents follow pseudo-second-order kinetic. Finally, the impact of coexisting ions and reusability was examined, with the FPSS adsorbent outperforming PSS. Therefore, the investigation of all these aspects demonstrated that the use of this natural surfactant significantly improves the performance of the adsorbent.

Effect of eco-friendly pervious concrete pavement with travertine waste and sand on the heavy metal removal and runoff reduction performance.

To address the negative environmental and economic impact of the large amounts of solid waste generated during travertine mining and to reduce the dependence on natural aggregates and cement for pervious concrete pavement applications, travertine waste, as aggregate and powder, was used for the travertine powder pervious concrete (TPPC) to improve the utilization of solid waste and decrease CO2 emissions. The experimental results showed that using 25% travertine aggregate and 5% powder results in a compressive strength reduction of only 9.8% to 25.92 MPa but a significant improvement in water permeability of 57.1% from 3.89 to 6.11 mm/s. To improve the performance of TPPC, further research was done on the effect of sand addition rate (SAR) on TPPC's density, compressive strength, porosity, water permeability, freeze-thaw resistance and heavy metal removal capacity to obtain an optimal incorporation ratio. As SAR rises, the compressive strength of TPPC with sand (STPC) initially increases and then decreases, while permeability behaves inversely. At 3% SAR, the compressive strength reached a maximum of 26.51 MPa, primarily due to the sand added to fill in some of the pores and stabilize the gradation. After 25 cycles, the strength loss rate of STPC varies from 11.39 to 17.93% and the freeze-thaw resistance is most excellent when SAR is 3%. The removal rate of heavy metals using the immersion method was found to be significantly higher (83.4-100%) compared to the rapid method (11.7-28.1%). Therefore, the 3% SAR was recommended for the mixture design of STPC. A laboratory-scale version of the pavement was constructed to assess the efficacy of STPC pavement (STPCP) in reducing runoff and removing heavy metals. The results showed that STPCP could remove more than 94% of runoff with varying intensities after 1 h. The STPCP exhibited removal rates ranging from 42.0 to 99.4% for Cd2+ and 79.5-95.4% for Cu2+. STPCP also attained a removal rate above 98% for Pb2+ after 30 min, demonstrating its environmental friendliness.

Bio-chelate assisted leaching for enhanced heavy metal remediation in municipal solid waste compost.

Municipal solid waste compost, the circular economy's closed-loop product often contains excessive amounts of toxic heavy metals, leading to market rejection and disposal as waste material. To address this issue, the study develops a novel approach based on: (i) utilizing plant-based biodegradable chelating agent, L-glutamic acid, N,N-diacetic acid (GLDA) to remediate heavy metals from contaminated MSW compost, (ii) comparative assessment of GLDA removal efficiency at optimal conditions with conventional nonbiodegradable chelator EDTA, and (iii) enhanced pre- and post-leaching to evaluate the mobility, toxicity, and bioavailability of heavy metals. The impact of treatment variables, such as GLDA concentration, pH, and retention time, on the removal of heavy metals was investigated. The process was optimized using response surface methodology to achieve the highest removal effectiveness. The findings indicated that under optimal conditions (GLDA concentration of 150 mM, pH of 2.9, retention time for 120 min), the maximum removal efficiencies were as follows: Cd-90.32%, Cu-81.96%, Pb-91.62%, and Zn-80.34%. This process followed a pseudo-second-order kinetic equation. Following GLDA-assisted leaching, the geochemical fractions were studied and the distribution highlighted Cd, Cu, and Pb's potential remobilization in exchangeable fractions, while Zn displayed integration with the compost matrix. GLDA-assisted leaching and subsequent fractions illustrated transformation and stability. Therefore, this process could be a sustainable alternative for industrial applications (agricultural fertilizers and bioenergy) and social benefits (waste reduction, urban landscaping, and carbon sequestration) as it has controlled environmental footprints. Hence, the proposed remediation strategy, chemically assisted leaching, could be a practical option for extracting heavy metals from MSW compost, thereby boosting circular economy.

Adsorption of Pb, Cu, and Ni Ions on Activated Carbon Prepared from Oak Cupules: Kinetics and Thermodynamics Studies.

Agricultural residue-activated carbon and biochar, inexpensive and environmentally friendly adsorbent materials, have recently received significant research attention. This study investigated the potential use of oak cupules in activated carbon form to remove widespread heavy metals (Pb2+, Cu2+, and Ni2+) from wastewater. The oak-activated carbon was prepared from oak cupules and activated with phosphoric acid. Oak-activated carbon was characterized using FTIR, BET analysis, energy-dispersive X-ray spectrometry (EDS), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The Freundlich, Langmuir, and Temkin isotherm models were used to assess the equilibrium data. The impact of various parameters, including pH effect, temperature, adsorbent dose, and contact time, was estimated. The Freundlich model was the most agreeable with Pb2+ adsorption by oak-based activated carbon, and Langmuir was more compatible with Cu2+ and Ni2+. Under optimum conditions, the average maximum removal was 63% Pb2+, 60% Cu2+, and 54% Ni2+ when every ion was alone in the aqueous solution. The removal was enhanced to 98% Pb2+, 72% Cu2+, and 60% Ni2+ when found as a mixture. The thermodynamic model revealed that the adsorption of ions by oak-based activated carbon is endothermic. The pseudo-second-order kinetic best describes the adsorption mechanism in this study; it verifies chemical sorption as the rate-limiting step in adsorption mechanisms. The oak-activated carbon was effective in removing Pb2+, Cu2+, and Ni2+ from wastewater and aqueous solutions.

Rapid aggregation of amyloid-like protein enhanced by mTGase to prepare functional wool fabrics for efficient and sustainable remove heavy metals from wastewater.

To counteract the increasing severity of water pollution and purify water sources, wastewater treatment materials are essential. In particular, it is necessary to improve the bonding strength between the adsorption material and the substrate in a long-term humid environment, and resist the invasion of microorganisms to prolong the service life. In this study, an amyloid-like aggregation method of lysozyme catalyzed by microbial transglutaminase (mTGase). Lysozyme self-assembles into an amyloid-like phase-transited lysozyme (PTL) in the presence of a reducing agent. Simultaneously, mTGase catalyzes acyl transfer reactions within lysozyme molecules or between lysozyme and keratin molecules, and driving PTL assembly on the wool fiber (TG-PTL@wool). This process enhances the grafting amount and fastness of PTL on the wool. Moreover, the tensile strength of wool fabric increased to 523 N. TG-PTL@wool achieves a 97.32 % removal rate of heavy metals, maintaining a removal rate of over 95 % after 5 cycles. TG-PTL@wool has excellent antibacterial property (99 %), and it remains above 90 % after 50 times of circulating washing. This study proved that mTGase can enhance the amyloid aggregation of lysozyme and enhance the bonding strength between PTL coating and substrate. Moreover, TG-PTL@wool provides a sustainable, efficient and cleaner solution for removing heavy metals from water.

Application and mechanism of carbonate material in the treatment of heavy metal pollution: a review.

Among the many heavy metal pollution treatment agents, carbonate materials show strong flexibility and versatility by virtue of their high adsorption capacity for heavy metals and the characteristics of multiple and simple modification methods. It shows good potential for development. This review summarizes the application of carbonate materials in the treatment of heavy metal pollution according to the research of other scholars. It mainly relates to the application of surface-modified, activated, and nano-sized carbonate materials in the treatment of heavy metal pollution in water. Natural carbonate minerals and composite carbonate minerals solidify and stabilize heavy metals in soil. Solidification of heavy metals in hazardous waste solids is by MICP. There are four aspects of calcium carbonate oligomers curing heavy metals in fly ash from waste incineration. The mechanism of treating heavy metals by carbonate in different media was discussed. However, in the complex environment where multiple types of pollutants coexist, questions on how to maintain the efficient processing capacity of carbonate materials and how to use MICP to integrate heavy metal fixation and seepage prevention in solid waste base under complex and changeable natural environment deserve our further consideration. In addition, the use of carbonate materials for the purification of trace radioactive wastewater and the safe treatment of trace radioactive solid waste are also worthy of further exploration.

Efficiency of magnetic zeolitic imidazolate framework-8 (ZIF-8) modified graphene oxide for lead adsorption.

Simple and efficient removal of Pb(II) ion from aqueous solution through adsorption has accelerated the development of many new composites to improve this popular method. In this study, the composites of graphene oxide (GO), zeolitic imidazolate framework-8 (ZIF-8), and magnetic materials were synthesized via coprecipitation method utilizing a different molar ratio between FeCl2 and FeCl3 of 1:0.5, 2:1, 3:1.5, and 4:2. The ZIF-8/GO was prepared via room temperature synthesis method prior to its further modification with magnetic materials for ease of separation. It was observed that the MZIF-8/GO2 of molar ratio 2:1 showed the best performance in adsorbing Pb(II) ion. As confirmed by FESEM image, it appeared to be ZIF-8 particles that have grown all over the GO platform and overlayed with Fe3O4 granular-shaped particles. The MZIF-8/GO2 successfully achieved 99% removal of Pb(II) within 10 min. The optimum values obtained for the initial concentration of Pb (II) were 100 mg/L, pH of 4 to 6, and adsorbent dosage used was 10 mg. The Langmuir isotherm and the pseudo-second-order kinetic model were deemed suitable to evaluate the adsorption of Pb(II) using MZIF-8/GO2. Results showed that MZIF-8GO2 achieved a maximum adsorption capacity of 625 mg/g of Pb(II) adsorption. All parent materials demonstrated a good synergistic effects, while exhibiting a significant contribution in providing active sites for Pb(II) adsorption. Therefore, this ternary composite of MZIF-8/GO2 is expected to be a promising adsorbent for Pb(II) adsorption from aqueous solution with an added value of ease of post phase separation using external magnetic field.

Investigation of the performance of the combined moving bed bioreactor-membrane bioreactor (MBBR-MBR) for textile wastewater treatment.

The present study focused on the investigation of the performance of a Moving Bed Bioreactor coupled with a Membrane Bioreactor (MBBR-MBR) on a small scale for textile wastewater treatment. The parameters examined in this study included the removal efficiency of chemical oxygen demand (COD), biochemical oxygen demand (BOD), total suspended solids (TSS), turbidity, color, and heavy metals (HM). The two reactors were operated consecutively and maintained aerobic conditions. The idea is to reduce the pollutant load significantly through the activity of microorganism attached to the biofilm covered carriers in MBBR and successive membrane filtration. The system demonstrated a favorable outcome even in a smaller hydraulic retention time (HRT) of 1 day, which presents a significant advantage in terms of cost and space saving. The removal effectiveness of COD attained a maximum of 92 %, BOD reached a maximum of 95 %, and the color removal performance obtained a removal efficiency of 87 %. Furthermore, the treatment showed remarkable efficiency in removing up to 100 % of TSS and 96 % of turbidity. Additionally, an evaluation was conducted on the elimination of heavy metals, including Zinc (Zn), Lead (Pb), Chromium (Cr), and Iron (Fe). The efficacy of removing these HMs was found to exceed 85 %. All these favorable outcomes contribute to the improvement of effluent quality, mitigation of contamination hazards, and fouling reduction.

Mechanisms for synergistically enhancing cadmium remediation performance of biochar: Silicon activation and functional group effects.

This work proposes an advanced biochar material (ß-CD@SiBC) for controllable transformation of specific silicon (Si) forms through endogenous Si activation and functional group introduction for efficient cadmium (Cd) immobilization and removal. The maximum adsorption capacity of ß-CD@SiBC for Cd(II) reached 137.6 mg g-1 with a remarkable removal efficiency of 99 % for 200 mg L-1Cd(II). Moreover, the developed ß-CD@SiBC flow column exhibited excellent performance at the environmental Cd concentration, with the final concentration meeting the environmental standard for surface water quality (0.05 mg L-1). The remediation mechanism of ß-CD@SiBC could be mainly attributed to mineral precipitation and ion exchange, which accounted for 42 % and 29 % of the remediation effect, respectively, while functional group introduction enhanced its binding stability with Cd. Overall, this work proposes the role and principle of transformation of Si forms within biochar, providing new strategies for better utilizing endogenous components in biomass.