Facile synthesis of lignin-based Fe-MOF for fast adsorption of methyl orange.

To rapidly remove dyes from wastewater, iron-based metal-organic frameworks modified with phenolated lignin (NH2-MIL@L) were prepared by a one-step hydrothermal method. Analyses of the chemical structure and adsorption mechanism of the NH2-MIL@L proved the successful introduction of lignin and the enhancement of its adsorption sites. Compared with NH2-MIL-101-Fe without phenolated lignin, the modification with lignin increased the methyl orange (MO) adsorption rate of NH2-MIL@L. For the best adsorbent, NH2-MIL@L4, the MO adsorption efficiency in MO solution reached 95.09% within 5 min. NH2-MIL@L4 reached adsorption equilibrium within 90 min, exhibiting an MO adsorption capacity of 195.31 mg/g. The process followed pseudo-second-order kinetics and the Dubinin-Radushkevich model. MO adsorption efficiency of NH2-MIL@L4 was maintained at 89.87% after six adsorption-desorption cycles. In mixed solutions of MO and methylene blue (MB), NH2-MIL@L4 achieved an MO adsorption of 94.02% at 5 min and reached MO adsorption equilibrium within 15 min with an MO adsorption capacity of 438.6 mg/g, while the MB adsorption equilibrium was established at 90 min with an MB adsorption rate and capacity of 95.60% and 481.34 mg/g, respectively. NH2-MIL@L4 sustained its excellent adsorption efficiency after six adsorption-desorption cycles (91.2% for MO and 93.4% for MB). The process of MO adsorption by NH2-MIL@L4 followed the Temkin model and pseudo-second-order kinetics, while MB adsorption followed the Dubinin-Radushkevich model and pseudo-second-order kinetics. Electrostatic interactions, π-π interactions, hydrogen bonding, and synergistic interactions affected the MO adsorption process of NH2-MIL@L4.

Harnessing iron materials for enhanced decolorization of azo dye wastewater: A comprehensive review.

Highly colored azo dye-contaminated wastewater poses significant environmental threats and requires effective treatment before discharge. The anaerobic azo dye treatment method is a cost-effective and environmentally friendly solution, while its time-consuming and inefficient processes present substantial challenges for industrial scaling. Thus, the use of iron materials presents a promising alternative. Laboratory studies have demonstrated that systems coupled with iron materials enhance the decolorization efficiency and reduce the processing time. To fully realize the potential of iron materials for anaerobic azo dye treatment, a comprehensive synthesis and evaluation based on individual-related research studies, which have not been conducted to date, are necessary. This review provides, for the first time, an extensive and detailed overview of the utilization of iron materials for azo dye treatment, with a focus on decolorization. It assesses the treatment potential, analyzes the influencing factors and their impacts, and proposes metabolic pathways to enhance anaerobic dye treatment using iron materials. The physicochemical characteristics of iron materials are also discussed to elucidate the mechanisms behind the enhanced bioreduction of azo dyes. This study further addresses the current obstacles and outlines future prospects for industrial-scale application of iron-coupled treatment systems.

Comparison of treatment performance and microbial community evolution of typical dye wastewater by different combined processes.

The degradation of typical dye wastewater is a focus of research in the printing and dyeing industry. In this study, a combined micro-electrolysis and microbial treatment method was established to treat refractory dye wastewater, and the pivotal factors in the microbial treatment were optimized. In the series and coupled modes, the removal rates of chroma reached 98.75% and 92.50%, and the removal rates of chemical oxygen demand (COD) reached 96.17% and 82.29%, respectively. The high-throughput sequencing results showed that the microbial communities in the microbial system varied at different treatment stages. From the culture stage to the domestication stage, the dominant phylum was Proteobacteria; however, the community abundance of microorganisms decreased. A combination of micro-electrolysis and biological methods can alter the characteristics of the microbial community, increase the number of dominant phyla, and increase the abundance of microorganisms. The degradation effect of the series mode and the overall strengthening effect of micro-electrolysis on the microorganisms were better than those of the coupled mode. In actual wastewater, the maximum removal rates of chroma, COD, total nitrogen (TN), ammonia nitrogen (NH3-N), and total phosphorus (TP) are 97.50%, 98.90%, 94.35%, 93.95%, and 91.17%, respectively. Three-dimensional fluorescence spectrum analysis showed that microbial processes could significantly degrade fluorescent components in wastewater, and methanogenic active enzymes in anaerobic processes could continue to react. The combined process can realize the efficient treatment of toxic dye wastewater by reducing the toxicity of wastewater and efficiently degrading organic matter, which has important guiding significance for the treatment of refractory dye wastewater.

Synergistic molecular mechanism of degradation in dye wastewater by Rhodopseudomonas palustris intimately coupled carbon nanotube - Silver modified titanium dioxide photocatalytic composite with sodium alginate.

The intimately coupled photocatalysis and biodegradation (ICPB), which combined the advantages of high oxidation capacity of photocatalysis and high mineralization rate of biodegradation, has demonstrated excellent removal performance in the degradation of azo dyes with highly toxic, refractory, mutagenic and carcinogenic. In order to explore the metagenomics mechanism of the ICPB system, a novel ICPB was prepared by coupling Rhodopseudomonas palustris (R. Palustris), carbon nanotube - silver modified titanium dioxide photocatalytic composite (CNT-Ag -TiO2, CAT) and sodium alginate (SA) (R. palustris/CAT@SA, R-CAT). Metagenomics sequencing was used to investigate the molecular mechanism of adaptation and degradation of dyes by photosynthetic microorganisms and the adaptive and synergistic interaction between photosynthetic microorganisms and photocatalyst. Experiments on the adaptability and degradability of photosynthetic microorganisms have proved that low concentration azo dyes could be utilized as carbon sources for growth of photosynthetic microorganisms. Metagenomics sequencing revealed that R. palustris was the main degrading bacterium in photosynthetic microorganisms and the functional genes related to carbohydrate metabolism, biological regulation and catalytic activity were abundant. It was found that the addition of photocatalyst significantly up-regulated the functional genes related to the catabolic process, electron transport, oxidoreductase activity and superoxide metabolism of organic matter in the photosynthetic microorganisms. Moreover, many key gene such as alpha-amylase, 1-acyl-sn-glycerol-3-phosphate acyltransferase, aldehyde dehydrogenase enrichment in microbial basal metabolism, such as enoyl-CoA hydratase, malate dehydrogenase, glutathione S-transferase enrichment in degrading azo dyes and electron transport, and many key gene such as undecaprenyl-diphosphatase, carbon storage regulator, DNA ligase enrichment in response to dyes and photocatalysts were discovered. These findings would contribute to a comprehensive understanding of the mechanism of degradation of dye wastewater by ICPB system, a series of genes was produced to adapt to environmental changes, and played synergistic role in terms of intermediate product degradation and electron transfer for degrading azo dyes. The photosynthetic microorganisms might be a promising microorganism for constructing ICPB system.

Boron Bifunctional Catalysts for Rapid Degradation of Persistent Organic Pollutants in a Metal-Free Electro-Fenton Process: O2 and H2O2 Activation Process.

Metals usually served as the active sites of the heterogeneous bifunctional electro-Fenton reaction, which faced the challenge of poor stability under acidic or even neutral conditions. Exploring a metal-free heterogeneous bifunctional electro-Fenton catalyst can effectively solve the above problems. In this work, a stable metal-free heterogeneous bifunctional boron-modified porous carbon catalyst (BTA-1000) was synthesized. For the BTA-1000 catalyst, the yield of H2O2 (294 mg/L) significantly increased. The degradation rate of phenol by BTA-1000 (0.242 min-1) increased by an order of magnitude, compared with the porous carbon catalyst (0.0105 min-1). The BTA catalyst could rapidly degrade industrial dye wastewater, and its specific energy consumption was 5.52 kW h kg-1 COD-1, lower than that in previous reports (6.38-7.4 kW h kg-1 COD-1). DFT and XPS revealed that C═O and -BC2O groups jointly promoted the generation of H2O2, and the -BCO2 group played dominant roles in the generation of •OH because the oxygen atom near the electron-giving groups (-BCO2 group) facilitated the formation of hydrogen bond and H2O2 adsorption. This work gained deep insights into the reaction mechanism of the boron-modified porous carbon catalyst, which helped to guide the development of metal-free heterogeneous bifunctional electro-Fenton catalysts.

Electrostatic deposition of TiO2 nanoparticles on porous wood veneer for improved membrane filtration performance and antifouling properties.

Wood has been a promising water purifier material on account of its abundant natural transport channels, easy processing, and renewability, which is mainly focused on its utilization in growth direction for effective separation.Wood veneer manufacured from raw wood block has a reversed-tree pore structure, and possesses advantages of low cost, easy fabrication, material saving, and abundant sources. To realize its functionalization and practicable application for membrane separation, modification of wood veneer is prerequisite. Herein, thin wood veneer with disparate utilization direction of wood was developed to design filter membrane loading TiO2 nanoparticles for treatment of dye wastewater. Wood veneer with reversed-tree transport pathways exhibits unique porous structure, and filtering direction and wood growth direction is almost orthogonal generated numerous sinuous channels. Thereout, sufficient area for loading TiO2 nanoparticles and contacting pollutants as well as appropriate water transport pathways at significantly shrinking thickness of wood (the thickness of 0.2 mm) can be provide by these sinuous channels. TiO2 nanoparticles was first modified by (3-Aminopropyl)triethoxysilane with high positive charge, and immobilized on negatively charged wood surface through atmospheric impregnation via strong electrostatic attractive interaction. Vast quantities of exposed TiO2 nanoparticles on wood cell lumens significantly enhance the adsorption ability for dye contaminants, resulting in a high membrane separation performance. The flux of TiO2/wood veneer membrane can achieve high level of 636.94 L/(m2h) with considerable methylene blue removal of 99.9% at 0.01 MPa. Meanwhile, it shows good cycling stability as well as decent flexibility and excellent mechanical strength. Moreover, the designed membrane with photocatalytic function of TiO2 also displays impressive decontaminated and recycling ability. The flux can recover its pre-recession level after 10 h light irradiation. The designed TiO2/wood veneer with simple preparation process and excellent water treatment capacity exhibits promising results for practical wastewater treatment.

Optimization of dye-contaminated wastewater treatment by fungal Mycelial-light expanded clay aggregate composite.

Dye-contaminated wastewaters from the printing batik industry are hazardous if discharged into the environment without any treatment. Finding an optimization and reusability assessment of a new fungal-material composite for dye-contaminated wastewater treatment is important for efficiency. The study purposes to optimize fungal mycelia Trametes hirsuta EDN 082 - light expanded clay aggregate (myco-LECA) composite for real priting batik dye wastewater treatment by using Response Surface Methodology with Central Composite Design (RSM-CCD). The factors included myco-LECA weight (2-6 g), wastewater volume (20-80 mL), and glucose concentration (0-10%) were applied for 144 h of incubation time. The result showed that the optimum condition was achieved at 5.1 g myco-LECA, at 20 mL wastewater, and at 9.1% glucose, respectively. In this condition, the decolorization values with an incubation time of 144 h were 90, 93, and 95%, at wavelengths 570, 620, and 670 nm, respectively. A reusability assessment was conducted for 19 cycles and the result showed that decolorization effectiveness was still above 96%. GCMS analysis showed the degradation of most compounds in the wastewater and the degradation products of the wastewater demonstrated detoxification against Vigna radiata and Artemia salina. The study suggests that myco-LECA composite has a good performance and therefore is a promising method for the treatment of printing batik wastewater.

Fe, N, S co-doped cellulose paper carbon fibers as an air-cathode catalyst for microbial fuel cells.

The heteroatoms and transition metal co-doped carbon-based catalysts are an important way to improve the catalytic activity of oxygen reduction reaction (ORR). Herein, we reported a facile method to obtain iron, nitrogen, and sulfur co-doped cellulose paper carbon fibers as catalysts (Fe-N-S/CFs) for ORR in microbial fuel cells (MFCs) with the adsorption recovery of Congo red molecules from dye wastewater. The thermal treatment promoted the etching of carbon surface by ferric ions, resulting in increased surface roughness for forming the defective carbon structure. The rich active species and defective carbon formed on the etched surface to enhance the electroactive surface area and effective sites. Fe-N-S/CFs catalysts achieved high half-wave potential due to the synergy effect between chemical components and defect structures. The assembled single-chamber air cathode MFC gained a high maximum power density of 1773 ± 40 mW m-2 versus Pt/C MFC of 1325 ± 94 mW m-2. This work provides a strategy for recovering dye molecules from wastewater to prepare non-precious metal catalysts for enhancing ORR activity.

Adsorption study of Methylene blue dye: an effluents from local textile industry using Pennisteum pupureum (elephant grass).

This study evaluates the adsorptive capacity of elephant grass (EG) in the removal of Methylene blue (MB) dye from wastewater sourced from two major local dyeing industries in Ogun State, Nigeria. Batch adsorption method was used to determine the optimum conditions, characterization of the adsorbent, equilibrium Isotherm models, kinetics and thermodynamics studies were conducted to evaluate the nature of the adsorption process. The optimum adsorption conditions obtained for the standard solution of MB dye were; pH 7, Temp 40 °C, contact time 180 min and adsorbent dosage 2.0 g. The presence of oxygen containing functional groups and shift or disappearance of bands in the FTIR suggested the suitability of EG for the process. The SEM of EG revealed presence and disappearance of pores before and after the adsorption process. The mechanism of this adsorption is complex, the adsorption data is best fitted to Langmuir isotherm, the mean adsorption energy E (≤6.455 kJ/mol), and activation energy (10.84 kJ/mol) represents physical process but, the thermodynamic studies revealed spontaneity (ΔG° -15.93 to -14.26 kJ mol-1), randomness, and endothermic (ΔH° 40.1 kJ/mol) nature, representing chemisorption. Therefore, local dyers around the study sites can make use of the freely available EG for the remediation of their wastewater.

Elephant grass (EG) abundantly thrives on the study sites where dye wastewater is released by local dyers. This serves as the impetus for this research as no other plants thrive on the dye-polluted environment. A favorable adsorption was obtained with EG as adsorbent for the Methylene blue (MB) dye that is a major constituent of the wastewater from the two major local dyeing industries investigated. Therefore, this study provides scientific support for the local dyers around the study sites to make use of the freely available EG for the remediation of their wastewater.

A novel titanium sulfate modified poly-magnesium-silicate coagulant with improved pH range for dye removal.

Coagulation with inorganic Mg-based coagulants is an efficient technology for dyes removal. However, the promising poly-magnesium-silicate (PMS) coagulant with better aggregation abilities can only be used in a very limited pH range. In this study, poly-magnesium-titanium-silicate (PMTS) was prepared by using titanium sulfate modified PMS. For the treatment of Congo red dye wastewater, PMTS(S), PMTS(Cl) and PMTS(N) synthesized under different acid media (H2SO4, HCl and HNO3) were used. PMTSs had the highest coagulation efficiency at Ti/Mg molar ratio of 0.75 and B value of 1.5. PMTSs outperformed PMS in the initial pH range of 5.50-9.00, with a dye removal efficiency of over 90% at 17.1 mg/L. Under optimal conditions, PMTS(S) had higher coagulation efficiency than that of PMTS(Cl) and PMTS(N), and the settling rate of the four Mg-based coagulants followed an order of PMTS(S) > PMS > PMTS(Cl) > PMTS(N). The coagulation mechanisms of PMTSs on Congo red dye were elucidated by further analysis of coagulation precipitates using UV, FT-IR, SEM and EDS. These results showed that the basis mechanism for floc formation was charge neutralization, while the key to floc formation was chemical combination. Based on the SEM and FTIR results, PMTSs could be found to have special shapes and chain structures, such as Si-O-Ti, Si-O-Mg, Ti-O-Ti, Mg-OH and Ti-OH. Combined with the results of zeta potential, the dominant mechanisms of PMTSs were more likely to be adsorption-interparticle bridging and net-sweeping. In a word, this study provided a highly efficient coagulant with a wide range of applicable pH for the control of dye contamination, and shed light on the potential application of PMTS in the removal of dye pollutants.

The Development and Synthesis of a CdZnS @Metal-Organic Framework ZIF-8 for the Highly Efficient Photocatalytic Degradation of Organic Dyes.

The development of photocatalysts for organic degradation is a hot research topic. In this study, CdZnS was selected as the carrier, and ZIF-8 was combined with it to explore the photocatalytic performance of the composite. In addition, the compound material, CdZnS@ZIF-8, was used as a photocatalyst for the decomposition of methylene blue dye, and the performance of pure CdZnS and pure ZIF-8 was compared. The photocatalytic efficiency of CdZnS@ZIF-8 was significantly higher than that of the other two. In the experimental reaction, the amount of catalyst was 0.04 g, the pH value was 7, the initial concentration of methylene blue aqueous solution was 20 mg/L, and the degradation of methylene blue in 50 mL aqueous solution could reach 99.5% under visible light irradiation for 90 min, showing excellent photocatalytic efficiency in the visible light range. It demonstrated excellent photocatalytic function in the visible light region, and the electron transfer phenomenon at the interface occurred in the het-junction and the separation of the photo-generating electron-hole as an electron acceptor of ZIF-8 further promoted the photocatalytic effect.

Effect of Enhanced Hydrolytic Acidification Process on the Treatment of Azo Dye Wastewater.

The hydrolysis acidification process is an economical and effective method, but its efficiency is still low in treating azo dye wastewater. It is therefore crucial to find more suitable and efficient means or techniques to further strengthen the process of treating azo dye wastewater by a hydrolytic acidification process. In this study, a hydrolytic acidification aerobic reactor was used to simulate the azo dye wastewater process. The change of wastewater quality during the reaction process was monitored, and the deep enhancement effect of single or composite biological intensification technology on the treatment of azo dye wastewater by the hydrolytic acidification process was also explored. Co-substrate strengthening and the addition of fructose co-substrate can significantly improve the efficiency of hydrolytic acidification. Compared with the experimental group without the addition of fructose, the decolorization ratio of wastewater was higher (93%) after adding fructose co-substrate. The immobilization technology was strengthened, and the immobilized functional bacteria DDMZ1 pellet was used to treat the simulated azo dye wastewater. The results showed that the composite technology experimental group with the additional fructose co-matrix had a better decolorization efficiency than the single immobilized bio-enhancement technology, with the highest decolorization ratio of 97%. As a composite biological intensification method, the fructose co-matrix composite with immobilized functional bacteria DDMZ1 technology can be applied to the treatment of azo dye wastewater.

Electrochemical removal of synthetic methyl orange dyeing wastewater by reverse electrodialysis reactor: Experiment and mineralizing model.

In this paper, the synthetic methyl orange (MO) dyeing wastewater treated by a reverse electrodialysis reactor (REDR) with 40 member pairs was investigated first. The boron-doped diamond (BDD) and carbon felt were adopted as an anode and a cathode in the REDR. The influences of operation parameters on the chemical oxygen demand (COD) removal efficiency were detected and explored. Then, a mathematical model of organic mineralizing was developed for the REDR to predict the variation of COD removal efficiency with treating time under the different operation conditions. Finally, the energy consumption of the wastewater treated by the REDR was analyzed. The results showed that raising the working fluid flowing velocity and electrode rinse solution flowrate improved the COD removal efficiency and instantaneous current efficiency (ICE), and reduced the total energy consumption (TEC) of the REDR. Raising the initial MO concentration could significantly reduce the TEC despite the COD removal efficiency being near. Since the main energy consumed by the REDR was salinity gradient energy (SGE) from waste heat conversion or the natural environment, the energy cost of REDR treating wastewater has been reduced significantly.

Ultrasound-enhanced catalytic degradation of simulated dye wastewater using waste printed circuit boards: catalytic performance and artificial neuron network-based simulation.

Recent developments of heterogeneous advanced oxidation for refractory organic contaminants and catalysts made of solid waste have attracted much attention. In this work, waste printed circuit board (wPCB) was used for catalytic degradation of simulated textile wastewater enhanced by ultrasound. Catalytic degradation of rhodamine B (RhB) and methylene blue (MB) was conducted in the presence of H2O2. Effect of ultrasound, wPCB, H2O2, pH, and dye concentration was investigated by single factor experiments. The growing catalytic efficiency was determined by ultrasound. The removal efficiency of MB and RhB are influenced by wPCB, H2O2, pH, and dye concentration. Degradation efficiency is accelerated with increasing wPCB dosage and H2O2 and decreasing dye concentration. Effective degradation of MB and RhB is obtained under broader pH region, attractively at neutral pH. Under optimal conditions, MB removal reaches 98.83% at 90 min while RhB removal reaches 99.57% at 80 min. Hydroxyl radicals play an important role in catalytic process. Tentative mechanism for catalytic degradation of MB and RhB are discussed based on multiple characterizations. Superior reusability of wPCB proves that wPCB is highly durable catalyst. Due to low cost and high efficiency, wPCB is attractive as effective catalyst for treatment of organic wastewater. Artificial neuron network-based (ANN) simulation, as a widely used artificial intelligence algorithm, was one of preferred methods for the wastewater treatment due to its unique properties in solving complex processes. An ANN model was designed for the prediction of the performance of ultrasound-enhanced catalytic degradation with a high R value (0.99).

Cost-effective resource utilization for waste biomass: A simple preparation method of photo-thermal biochar cakes (BCs) toward dye wastewater treatment with solar energy.

Waste biomass and dye wastewater pollution have been the serious environmental problems. The interfacial solar-steam generation technology is an effective and sustainable method for the water purification. However, the complex preparation process, high economic cost and probably secondary environmental pollution of traditional photo-thermal materials restricted their practical large-scale application. Herein, the biochar cakes (BCs) deriving from waste biomass were prepared, and the granular and schistose MgO coatings were dressed on the surface of carbonized fiber to improve their hydrophilicity. The BCs with high solar absorbance and super-hydrophilicity were applied in the photo-thermal purification of dye wastewater with solar energy. The highest evaporation rate of dye wastewater with BCs reached 2.27 kg m-2 h-1, and the corresponding conversion efficiency of solar to steam generation was 78.98% under the simulated solar irradiation (1846.0 w/m2). The collected clean water from the solar-steam evaporators reached the emission standards of EU Water Framework Directive (91/271/EEC). Considering the simple and economical preparation method, this process made the practical large-scale application of photo-thermal BCs on dye wastewater treatment a reality, and also provided a cost-effective management strategy for the waste biomass.

Advanced treatment of dye wastewater using a novel integrative Fenton-like/MnO2-filled upward flow biological filter bed system equipped with modified ceramsite.

The deposal of residual hydrogen peroxide (H2O2) in Fenton-like system and the requirement of oxygen in bioreactor are essential parts for the treatment of integrative Fenton-like/bioreactor. A novel low-cost integrative Fenton-like and MnO2-filled upward flow biological filter bed (Fenton-like/MBFB) equipped with the modified ceramsite was constructed to evaluate the main properties and catalytic activity of modified ceramsite, and the optimal conditions of integrative system and compare integrative and traditional systems. In this study, the Fenton-like reactor with modified ceramsite had higher catalytic ability whose Acid Orange 7 (AO7) degradation efficiency reached to 79.3% due to large surface area and high porosity, compared with that with raw ceramsite (44.3%). Furthermore, total utilization efficiency of H2O2 in integrative system (from 32.41% to 53.51%) and removal efficiencies of COD and AO7 were remarkably improved, which would effectively decrease the waste of H2O2 and the setting of regulation pool and aeration tank. Thus, the integrative system can save 0.51 CNY/m3 in construction cost and 0.21 CNY/m3 in operating cost. The average COD removal efficiency, AO7 degradation efficiency and effluent DO concentration were achieved to 64.8%, 79.5% and 9.3 mg/L respectively in integrative system were achieved in integrative system during sixty successive runs. Also, the potential degradation pathway of contaminants was also proposed according to the OH-enhanced at Fenton-like reactor due to catalyst and adsorption of modified ceramsite and the removal of microorganisms and modified ceramsite for contaminants at MBFB. This study demonstrated the feasibility of integrative Fenton-like/MBFB filled with modified ceramsite for simultaneously decreasing operational cost and complexity and enhancing removal efficiency, thus provided a one-step alternative for refractory dye wastewater.

Fabrication of chitosan-aminopropylsilane graphene oxide nanocomposite hydrogel embedded PES membrane for improved filtration performance and lead separation.

In the present study chitosan-aminopropylsilane graphene oxide (CS-APSGO) nanocomposite hydrogel was synthesized and utilized as a hydrophilic additive in different dosages (0.5, 1, 2 and 5 wt%) in fabrication of porous polyethersulfone (PES) membranes via the phase inversion induced process by immersion precipitation method for heavy metal ion and dye removal. The modified membranes were characterized using ATR-FTIR, AFM, SEM, water contact angle, overall porosity and mean pore radius evaluations and zeta potential measurement. The addition of CS-APSGO nanocomposite hydrogel to PES doping solutions enhanced membranes hydrophilicity and consequently pure water flux permeability. Filtration performance of the CS-APSGO embedded membranes showed promising antifouling properties during BSA filtration test (FRR> 90%) and 1 wt% membranes showed the highest pure water flux of 123.8 L/m2 h with BSA rejection more than 98% and removal capability more than 82% for lead (II) ion, 90.5% and 98.5% for C.I. Reactive Blue 50 and C.I. Reactive Green 19, respectively. Therefore, the CS-APSGO nanocomposite hydrogel blending in order to modification of PES-based membranes have a noticeable potential in improving filtration performance of blended membranes.

Textile Dye Biodecolorization by Manganese Peroxidase: A Review.

Wastewater emissions from textile factories cause serious environmental problems. Manganese peroxidase (MnP) is an oxidoreductase with ligninolytic activity and is a promising biocatalyst for the biodegradation of hazardous environmental contaminants, and especially for dye wastewater decolorization. This article first summarizes the origin, crystal structure, and catalytic cycle of MnP, and then reviews the recent literature on its application to dye wastewater decolorization. In addition, the application of new technologies such as enzyme immobilization and genetic engineering that could improve the stability, durability, adaptability, and operating costs of the enzyme are highlighted. Finally, we discuss and propose future strategies to improve the performance of MnP-assisted dye decolorization in industrial applications.

Biochar-activated persulfate for organic contaminants removal: Efficiency, mechanisms and influencing factors.

Turning biomass into biochar as a multifunctional carbon-based material for water remediation has attracted much research attention. Sawdust and rice husk were selected as feedstock for biochar (BC) production, aiming to explore their performance as a catalyst to activate persulfate (PS) for degrading acid orange 7 (AO7). There was an excellent synergistic effect in the combined BC/PS system. Sawdust biochar (MX) showed a faster and more efficient performance for the AO7 degradation due to its abundant oxygen functional groups, compared to rice husk biochar (DK). In the BC/PS system, AO7 was well decolorized and mineralized. Based on the two-dimensional correlation analysis method, the azo conjugation structure and naphthalene ring of AO7 molecule changed first then benzene ring changed during the reaction. Moreover, AO7 decolorization efficiency increased with the increase of PS concentration and biochar dosage, and the deacrease of pH. Biochar deactivated after used twice. When the biochar reached its adsorption equilibrium of AO7, the AO7 could not be degraded in the BC/PS system. SO4- and OH participated in the reaction together and OH played the main role in activating PS to AO7 decolorization based on the radical scavengers experiment. All of results indicate using biochar to activate PS for degradation of AO7 contaminated water is a promising method.

Improvement of polyvinyl chloride nanofiltration membranes by incorporation of multiwalled carbon nanotubes modified with triethylenetetramine to use in treatment of dye wastewater.

Multiwalled carbon nanotubes modified with triethylenetetramine (TETA) as an organic nanofiller was used in fabrication of polyvinyl chloride (PVC) nanofiltration membranes. The membranes were prepared by the phase separation method and immersion precipitation technique. For this purpose, various percentages of the TETA-MWCNTs were added to the casting solutions and the membrane films were formed and placed in a bath water. In order to identify the membranes and their properties, SEM images, contact angle and FTIR-ATR analyses were taken from the prepared nanocomposite membranes. The membranes performance in terms of water/protein/dye permeability, protein rejection and Lanasol blue 3R dye rejection were investigated. Establishing hydrogen bond between the water molecules and the functional groups of MWCNTs enhanced the hydrophilicity of the fabricated membranes and caused an increase in permeability. The permeability in the membrane containing 0.25 wt% of TETA-MWCNTs reached its highest value, and adding more amounts reduced flux by blocking the membrane pores. There was also a significant decrease in the rate of membrane fouling for the hybrid membranes. Flux recovery ratio reached from 62.2% to 76.1%. Also, rejection of BSA and Lanasol blue 3R combination dye was increased for the modified membranes.