Dye Removal Process Research Articles

Evaluation of the textile dye removal process using the residual substrate from Pleurotus ostreatus mushroom production

O lançamento de efluentes têxteis sem tratamento, ou submetidos a um tratamento ineficaz, ocasiona graves problemas nos ecossistemas aquáticos. Neste contexto, o objetivo deste estudo foi avaliar a capacidade e o processo de remoção do corante têxtil Drimaren Red CL-7B, empregando o substrato residual da produção do cogumelo Pleurotus ostreatus. Para tanto, primeiramente elaborado um planejamento experimental 3², considerando as variáveis pH e concentração de substrato, buscando-se avaliar a remoção de corante proveniente de efluente têxtil sintético, durante seis horas de tempo de contato. As concentrações do substrato aplicado ao efluente foram 50, 100 e 150 g L-1 e os valores de pH empregados foram 5, 7 e 9. Após a determinação da melhor condição experimental dentre as avaliadas, também foram estudados os possíveis mecanismos de remoção ocorridos e a atividade enzimática do micélio presente no substrato. Verificou-se que a melhor condição operacional foi obtida com pH 5 e concentração de 150 g L-1. Sob essas condições, a eficiência de remoção de corante alcançada foi próxima de 70%. Observou-se que o principal mecanismo de remoção foi a adsorção e um tempo de contato de 30 minutos já permite obter resultados satisfatórios. Além disso, os resultados da atividade da lacase demonstraram que sua eficiência é elevada em condições de pH ácido, e que esta fica inativa em condições de pH alcalino. Concluiu-se que o substrato residual apresenta elevado potencial para o tratamento de efluentes têxteis em decorrência da ação simultânea das enzimas lignolíticas e da adsorção na remoção de corantes, bem como, pela possibilidade de valorização de um resíduo agroindustrial.

Evaluation of Iron-Modified Biochar from Sugarcane Bagasse and Heterogeneous Fenton Process for Batik Dye Removal

Evaluation of Iron-Modified Biochar from Sugarcane Bagasse and Heterogeneous Fenton Process for Batik Dye Removal

Development of Luminescent and Photosensitive Cellulose Microfibers From Palm Sprout Fibers: Antibacterial Efficacy and Dye Adsorption Potential.

A key contemporary challenge is enhancing the value of agro-industrial byproducts. Cellulose, the most abundant renewable resource, offers significant industrial potential due to its versatile properties. Produced in its pure form by various bacteria, cellulose is increasingly utilized in microscale and nanoscale fibers for composite reinforcement. In this study, cellulose microfibers were derived from palm sprout fibers through a series of treatments like pretreatment, high-pressure hydrolysis in an autoclave, and bleaching. These fibers were then characterized using techniques such as UV spectroscopy, FTIR, SEM, and XRD. The study evaluated the antibacterial properties of the treated cellulose microfibers against both gram-positive Staphylococcus aureus (07%) and gram-negative Escherichia coli (10%), finding higher effectiveness against E.coli. Additionally, the microfibers exhibited a lower EC50 value of 0.101 mg/mL, suggesting that although the microfiber extract is effective, the standard antioxidant is somewhat more potent. Adsorption studies revealed that the cellulose microfibers followed the Langmuir isotherm model, with a high determination coefficient of 0.998, and reached maximum dye adsorption for RB 160 within 120 min. In this adsorption study, 50 mg of dye was removed. These results indicate that the treated cellulose microfibers are a promising biosorbent for improving dye removal processes.

Physicochemical Investigations of Magnetite Persulfate Ozone Hybrid System for the Removal of Tartrazine Dye from Aqueous Solution

ABSTRACT This study involved the synthesis of magnetite nanoparticles by co-precipitation method. The synthesized nanoparticles were subsequently evaluated for their catalytic efficacy in the degradation and ozonation of tartrazine dye (TTD), employing sodium persulfate as a catalyst both in the presence and absence of ozone. The material characterization revealed that synthesized Fe3O4 nanoparticles were proven to have a crystalline structure by XRD. While spherical agglomerates with a flower-like morphology were revealed by the SEM, similarly FT-IR detected Fe – O – Fe and O – H bond vibrations, boosting surface area and catalytic activity. The degradation of the TTD was assessed in a laboratory-scale reactor, and its progress was monitored using UV-visible spectrophotometry. A comparative analysis of the two methods revealed that the catalytic ozonation demonstrated superior efficacy compared to the catalytic degradation, achieving a maximum degradation of 94.35% within 25 min of contact time. Optimal degradation parameters included a TTD concentration of 50 ppm, magnetite dosage of 0.75 g, persulfate concentration of 8 mm, and ozone inlet concentration of 5 g/L at pH 3. Evaluation of the degradation kinetics indicated the second-order kinetics model as the most appropriate, suggesting a physicochemical nature of the dye removal process. Furthermore, the study demonstrates enhanced efficiency in TTD decomposition compared to conventional methods.

Rapid and efficient removal of water-soluble dyes via natural asphalt oxide as a new carbonaceous super adsorbent; NA-oxide synthesis and characterization

In this study, natural asphalt was oxidized to synthesize a new nano-structure adsorbent for dye removal. The functionalization of natural asphalt by oxidation introduced new properties that influenced its activity. The process of oxidizing natural asphalt with potassium permanganate resulted in a low-cost adsorbent, which can potentially be a more affordable option compared with synthetic alternatives. Characterization analysis confirmed the enhanced surface area, improving dye interaction and adsorption. The interconnected channels and capillaries of the oxidized natural asphalt facilitated the capillary action drawing in liquids, including dyes. The distinctive porosity of natural asphalt oxide (NA-oxide) was noted, and the experimental results showed that the NA–oxide nanoadsorbent efficiently adsorbed cationic and anionic dyes in water, with maximum capacities of 14.68 mg.g−1, 17.81 mg.g−1 and 16.47 mg.g−1 for methyl orange, methylene blue and Rhodamine B, respectively. The study investigated various parameters, such as concentration, adsorption dose, pH, contact time, and temperature, affecting the dye removal process. Langmuir, Freundlich, and Temkin isotherms along with pseudo-first and pseudo-second-order kinetic equations were applied to assess the adsorption process, indicating that dyes adhered to the pseudo-first-order model and Langmuir isotherm. Analysis of MO, MB, and RhB dyes revealed conformity to Langmuir isotherm and first-order kinetics. Thermodynamic evaluations like ΔH°, ΔS°, and ∆G° displayed the exothermic and spontaneous nature of dye adsorption on the NA-oxide adsorbent. Furthermore, the absorbent displayed remarkable stability with a recovery rate of 98.45% after ten cycles, signifying its potential for enduring effectiveness in dye removal processes.

Optimization study of methylene blue dye adsorption on Chamaerops humilis fibers biosorption using a central composite design

This research explores the effectiveness of Chamaerops humilis (CH) fibers as a biosorbent for the adsorption of Methylene Blue (MB) dye from aqueous solutions. The fibers were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR). To optimize the dye removal process, a Design of Experiments methodology, specifically Central Composite Design (CCD), was applied. Factors such as solution pH, adsorbent dosage, contact time, and temperature were varied. The CCD analysis identified the optimal conditions for maximum removal efficiency (99.87 %) of a 10 mg/L MB solution, which were: 1.06 g/L of CH fiber dosage, pH 9.6, and a contact time of 60 min. The adsorption process aligned well with a pseudo-second-order kinetic model, and the maximum adsorption capacity of CH fibers was determined to be 9.422 mg/g. Thermodynamic parameters, including Gibbs free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) changes, were calculated, confirming that the adsorption is spontaneous and endothermic. The study highlights the potential of Chamaerops humilis fibers as an efficient and eco-friendly adsorbent for MB dye removal, offering a sustainable and cost-effective solution for wastewater treatment, particularly in industrial effluent management.

Preparation of Cu-doped MIL-125(Ti)-derived carbon-based composites for the sonodynamic degradation of organic dyes

Sonocatalysis provides a green and sustainable strategy to remove industrial organic pollutants. Toward improving the sonocatalytic performance to remove the organic dyes, a new Cu-C@TiO2 catalyst was prepared via doping the Cu(II) ions into the MIL-125(Ti) and then carbonizing the resultant Cu-MIL-125(Ti) in this study. By the SEM, EDS and BET, the obtained Cu-C@TiO2 was a porous carbon-based hybrid with bimetallic centers, retaining a large amount of organic frameworks to supply adequate specific surface area for the adsorption; By the XPS and UV–vis DRS, the band gap of Cu-C@TiO2 was reduced to significantly broaden the light absorption region and facilitate the separation of electron-hole pairs; By the fluorescence spectra, the graphite-like structure and Cu particles produced on the catalyst surface served as an electron trap to inhibit the recombination of charge carriers. The Cu-C@TiO2 showed an excellent sonocatalytic performance to organic dyes, and under the ultrasound irradiation (35 KHz, 150 W), it could remove more than 95 % of rhodamine B (5.00 mg/L) and methylene blue (5.00 mg/L) within 10 min. By the kinetic analysis, it was found that the dye removal obeyed the first-order kinetic model, and the scavenging studies of free radicals (OH and O2−) verified the Cu-C@TiO2-mediated sonodynamic degradation was in the dye removal. In the end, a Cu-C@TiO2-mediated adsorption/sonodynamic degradation mechanism was proposed to thermodynamically expound the removal process of organic dyes.

Effective removal of textile dye via synergy of adsorption and photocatalysis over ZnS nanoparticles: Synthesis, modeling, and mechanism

In this work, we prepared sulfur-zinc nanoparticles (ZnS-TGA) functionalized with thioglycolic acid by a hydrothermal method and tested their photodegradation ability by solar irradiation. ZnS-TGA were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), high-resolution transmission electron microscope (HR-TEM), UV–Vis spectrophotometer and photoluminescence spectroscopy. In the characterization of these nanoparticles, thioglycolic acid proved to be a strong capping ligand, with a specific surface area of 36.82 m2/g and an average size of 7.15 nm. To test the photocatalytic degradability of the product, methylene blue (MB) was used as a model pollutant. Various operational variables were investigated, including pH, amount of nanoparticles, dye concentration, contact time and temperature. The equilibrium adsorption tests, and the statistical physical calculations allowed the analysis of the energetic and steric variables of the adsorption of MB dye molecules on the surface of these nanoparticles. The equilibrium data were well fitted with Langmuir-Freundlich (L-F) and the adsorption kinetics with pseudo-first order. The maximum adsorption capacity of the MB dye removal process was 30.92 mg g−1 at pH 7 and 298 K, and this process was spontaneous and exothermic. The dye molecules and the surface of the nanoparticles exhibited physical interactions with adsorption energies of 23.31–25.92 kJ/mol. The photocatalytic activity of these nanoparticles resulted in a dye degradation efficiency of 91.1 % in 180 min. The photocatalytic efficiency remained almost unchanged after five consecutive degradation cycles, resulting in a methylene blue degradation of 85 %. According to these results, these environmentally friendly nanoparticles have the potential to purify industrial and urban liquids contaminated with harmful organic compounds such as dye molecules.

FACILE SYNTHESIS OF ACTIVATED CARBON/ALGINATE/CHITOSAN COMPOSITE BEADS AS RHEMAZOLE BRILLIANT BLUE R ADSORBENT

Developing composite beads composed of chitosan, alginate, and activated carbon for dye removal is essential due to their improved adsorption capabilities and environmental benefits. By utilizing natural resources efficiently for an effective dye removal process, this study developed an activated carbon/alginate/chitosan composite bead as Rhemazole Brilliant Blue R (RBBR) adsorbent. The surface shape of composites exhibits more protrusions, grooves, and asymmetric pores than activated carbon, which could improve dye adsorption capability. FTIR analysis verified that functional groups such as OH, NH, protonated amine, and carboxylate from the constituent polymers were enriched in the activated carbon/alginate/chitosan composite. These groups also function as active sites for adsorbents. It was aligned with the composite beads' Freundlich isotherm model, which shows that heterogeneous or many active sites contribute to adsorption and provide multilayer adsorption. The kinetic model of pseudo-second order fits well with the adsorption process, indicating that chemisorption is the rate-limiting step in RBBR adsorption. The optimum adsorption conditions were at pH 1, with an adsorbent dose of 0.08 g, RBBR dye concentration of 125 mg/L, and a contact time of 60 min. The composite beads also exhibit stability in acidic and basic solutions, with the effectiveness of being reused up to four times, providing a reusable adsorbent with versatility in various water treatment conditions. Hence, synthesizing activated carbon/alginate/chitosan composite beads presents a promising solution for sustainable wastewater treatment based on biodegradable and eco-friendly composite.

Adsorption dynamics of Eriochrome Black dye removal using raw and ultrasonicated Pithecellobium seed biomass: ANN modeling and mechanisms

Utilization of Ultrasonic modified Pithecellobium dulce seed biomass, proved the efficacy in Eriochrome black dye remediation. The study investigates the sorption dynamics of Eriochrome Black (EB) dye removal using raw and ultrasonicated Pithecellobium seed biomass combined with Artificial Neural Network (ANN) modeling for the elucidation of underlying mechanisms. To improve the adsorption performance, Pithecellobium dulce biomass has been subjected to ultrasonication. The characterization of modified seed adsorbent revealed the adsorptive properties of biomass for the removal process. Varying impacts of dye adsorption were studied revealing the optimal parameters to be pH of 5, temperature of 303 K, contact time of 40 min-Ultrasonicated Pithecellobium dulce (UPDB) biomass; 80 min – Raw Pithecellobium dulce biomass (RPDB), and dose of 5 g/L and 2.5 g/L for RPDB and UPDB respectively. Isotherm and Kinetic analysis revealed the Freundlich and pseudo-first order models to be best fitting for the current system. Ultrasonicated seed biomass exhibited enhanced adsorption capacity of 126.9 mg/g compared to 83.8 mg/g for raw seed biomass. Thermodynamic investigation infers the spontaneity and exothermic nature of adsorption process. The ANN model for the prediction of eriochrome black dye adsorption onto ultrasonic modified Pithecellobium dulce seed biomass exhibited better correlation coefficient of 0.9559 indicating the better prediction of trained model for dye removal process. Thus, ANN model provides a better prediction of the relation between operational factors and dye removal.

Magnetic pomegranate peels activated carbon (MG-PPAC) composite for Acid Orange 7 dye removal from wastewater

A magnetic pomegranate peels activated carbon (MG-PPAC) nanocomposite (23.46–26.75 nm) was prepared as an effective adsorbent for Acid Orange 7 (AO7) dye removal from wastewater. The effects of impregnation ratio and activation temperatures (600–900 °C) on the specific surface area and pore morphology were studied. BET, SEM, EDX, FT-IR, XRD and VSM are considered the synthesized composite MG-PPAC. The prepared magnetic composite at 700 °C activation temperature and impregnation ratio 1/2 (peels/ZnCl2) exhibited 513.34 m2/g surface area, 0.4025 cm3/g volume of the total pores, and 3.1364 nm mean diameter of the pores. The magnetization saturation, remanence and coercivity of the MG-PPA composite were 14.116 emu/g, 0.50685 emu/g, and 19.705 G, respectively. Also, the composite MG-PPAC was in a super-paramagnetic state at room temperature and could be gathered within 5 S (less than 5 S) with an external magnetic field. The impact of pH, adsorbent dose, initial concentration of adsorbate (AO7 dye), and time of contact have been studied to optimize the removal process. Langmuir, Freundlich and Temkin isotherm models were used to investigate MG-PPAC adsorption behavior for AO7 dye. Applicability of the Langmuir isotherm model demonstrates a monolayer adsorption AO7 dye removal process, and the maximum monolayer capacity (Qm) attained from linear solvation of LIM is 322.58 mg/g. Furthermore, the highest removal was 99.53% at pH 2.25. Also, the adsorption process was tested using like pseudo-first-order, pseudo-second-order, intraparticle diffusion, film diffusion, and Elovich models. The pseudo-second-order model is well-fitted to the operational data of AO7 dye removal.

Methylene blue dye removal by adsorption with coconut coir and acid-treated forms: adsorption-desorption study, MPR and modeling using artificial intelligence

A batch study is conducted to remove methylene blue (MB) dye from an aqueous solution using coconut coir and its acid-treated forms. The sulfuric acid-treated coconut coir (SCC), phosphoric acid-treated coconut coir (PCC) and untreated coconut coir (UCC) were prepared. Adsorbents were characterized via BET, SEM, pHPZC, FTIR, and FT-Raman analysis. Adsorbent’s total organic carbon (TOC) and the number of oxygen-containing functional groups like carboxylic, lactonic and phenolic, total acidic, and basic groups were also estimated. FTIR and FT-Raman studies establish functional groups responsible for dye removal. The operating parameters were optimized through experiments. Dye was removed maximally at the lowest temperature, 303K. Langmuir and Temkin isotherm models use linear equations, and the Pseudo-second-order kinetic model uses a nonlinear equation, which fits well. The adsorption capacity of SCC, PCC and UCC adsorbents was 88.18 ± 0.63 mg/g, 92.68 ± 2.74 mg/g and 76.39 ± 0.36 mg/g, respectively, for 303K. Intraparticle diffusion dominated more than film diffusion. Physisorption was estimated by applying the Dubinin-Radushkevich (D-R) isotherm model. Thermodynamic study indicates a spontaneous, favorable, exothermic process. 75% glacial acetic acid and 100% methanol are the best solvents for desorbing dye-loaded adsorbents. Porous coir and non-covalent interactions like hydrogen bonding, van der Waals force and π-π interaction between dye and coir are vital in the dye removal process. The regression equation has been successfully formulated, and the application of a genetic algorithm has predicted the percentage removal of methylene blue dye.

Immobilization of EPS-modified sodium alginate microcapsule by co-polymerization for methylene blue dye adsorption and kinetics

Exopolysaccharide (EPS) was extracted from Bacillus sp. and purified by ethanol precipitation method. This work mainly examines the dye removal efficiency of biopolymer beads (sodium alginate microcapsules) encapsulated with EPS extracted from Bacillus sp. Encapsulation of EPS-modified sodium alginate microcapsule was done by co-polymerization method. Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) confirmed the co-polymerization of sodium alginate and EPS in the microcapsule. The adsorption capacity of the microcapsule was found to be 0.58682 mg/mL which can be attributed to the larger surface area and increased surface sites in the microcapsule adsorbent. Increased dye removal efficiency of 83% was observed for the microcapsule with 50 mg/mL of EPS. The results of the methylene blue dye adsorption experiment show that the adsorption fitted into the Freundlich isotherm and followed pseudo-second-order reaction with correlation coefficients of 0.939 and 0.9673, respectively. The prepared sodium alginate biopolymer is biodegradable, and numerous studies have documented its biodegradability. Overall, these results evidenced that dye adsorption from textile effluent can be easily managed using the biodegradable polymer materials. Hence, this immobilization approach can be effectively used in textile dye removal process.

Exploring the diverse performance of nickel and cobalt spinel ferrite nanoparticles in hazardous pollutant removal and gas sensing performance.

A simple sol-gel combustion process was employed for the creation of MFe2O4 (M=Ni, Co) nanoparticles. The synthesized nanoparticles, acting as both photocatalysts and gas sensors, were analyzed using various analytical techniques. MFe2O4 (M=Ni, Co) material improved the degradation of methylene blue (MB) under UV-light irradiation, serving as an enhanced electron transport medium. UV-vis studies demonstrated that NiFe2O4 achieved a 60% degradation, while CoFe2O4 nanostructure exhibited a 76% degradation efficacy in the MB dye removal process. Furthermore, MFe2O4 (M=Ni, Co) demonstrated chemosensitive-type sensor capabilities at ambient temperature. The sensor response and recovery times for CoFe2O4 at a concentration of 100ppm were 15 and 20, respectively. Overall, the synthesis of MFe2O4 (M=Ni, Co) holds the potential to significantly improve the photocatalytic and gas sensing properties, particularly enhancing the performance of CoFe2O4. The observed enhancements make honey MFe2O4 (M=Ni, Co) a preferable choice for environmental remediation applications.

Enhancing dye/salt separation efficiency through polysulfobetaine-modified poly (triazine imide)/polyethersulfone (PTI-PSBMA/PES) composite membrane fabrication

Membrane technology stands as a vital solution for efficient dye/salt separation in various industrial processes. For the first time in this study, polysulfobetaine-modified poly (triazine imide) (PTI-PSBMA) was simply prepared by reversible addition-fragmentation chain-transfer (RAFT) polymerization as an additive for PTI-PSBMA/PES composite membrane preparation using the phase inversion strategy. The SEM, AFM pictures, and WCA analysis results exhibited that the modified membranes with PTI-PSBMA possess smoother surfaces and are more hydrophilic. After conducting an investigation using a dead-end filtration setup, it has been determined that the PTIZ-1 membrane, containing 1.0 wt% of PTI-PSBMA, emerged as the most effective membrane. This membrane exhibited a remarkable water flux of 46.0 L. m−2 h−1 bar−1 and demonstrated the highest rejections for various dyes, such as Reactive Red 120 (92.3 %), Direct Yellow 29 (79.3 %), and Methyl Green (85.0 %). Additionally, the PTIZ-1 membrane displayed impressive antifouling properties, with protein adsorption decreasing by over 96.0 %. With exceptional rejection rates for dyes and high permeability for salts, this composite membrane presents a promising solution for practical applications in wastewater treatment and dye removal processes. This research contributes to advancing membrane technology by introducing a highly efficient composite membrane with enhanced separation properties, addressing critical challenges in industrial dye/salt separation processes.

Nanocarrier optimization: Encapsulating Hydrastis canadensis in chitosan nanoparticles for enhanced antibacterial and dye degradation performance

This study focuses on the optimization of Hydrastis canadensis-based nanocarriers in environmental and microbial applications like antibacterial and dye degradation. Hydrastis canadensis (H. canadensis) is loaded into the nanocarrier using a gelation method. Characterization involves pH analysis, UV-VIS spectrophotometry, scanning electron microscopy, Fourier-transform infrared spectroscopy, dynamic light scattering, high-performance liquid chromatography, encapsulation efficiency. Further antimicrobial activity against Staphylococcus aureus and Escherichia coli were tested. Dye degradation was evaluated at concentrations of 1 % of high molecular (HM) and 1.5 % of low molecular (LM) chitosan nanoparticles with both 3C and 1000C concentrations of the drug. The obtained results confirm the presence of chitosan nanocarrier alongside the pure drug in 1 % HM and 1.5 % LM chitosan particles with a notable encapsulation efficiency activity in both 3C and 1000C concentrations. Antimicrobial studies were carried out using the agar well diffusion method and revealed a significant zone of inhibition of 20 mm and 25 mm for E. coli and S. aureus, respectively in chitosan nanocarrier-loaded samples compared to pure drug and chitosan nanocarriers samples. The dye degradation studies of four dyes methylene blue, methylene orange, methylene red, and safranin using both pure drugs and chitosan nanocarrier-loaded drugs showed the highest percentage of degradation (76 %) against methylene blue in the chitosan nanocarrier-drug loaded formulation. These findings cumulatively underscore chitosan nanoparticles can be used as an effective carrier for Hydrastis Canadensis, with enhanced antimicrobial and dye degradation capabilities. Varied concentrations and molecular weights highlight the versatility of the ionotropic gelation method in optimizing drug delivery. Enhanced efficacy of the nanocarrier was evident in the observed zone of inhibition in antimicrobial testing. The substantial degradation percentage in methylene blue emphasizes the formulation's applicability in environmental dye removal processes, with potential avenues for improvement explored through interactions between the chitosan nanocarrier and H. canadensis characteristics. Future investigations may focus on scaling up the optimized formulation for large-scale applications and exploring release kinetics and comprehensive toxicity assessments for a holistic understanding of potential environmental and biomedical implications.

Poly acrylonitrile Schiff-bases nanofibers: Antibacterial and dye removal potency

Polymer nanofibers exhibit a diverse range of applications in both biological and environmental contexts owing to their unique surface structure and porosity. This study investigates the synthesis of polyacrylonitrile (PAN) Schiff base nanofibers utilizing an electrospinning protocol and their antibacterial potency as well as their dye-removing capability. Schiff bases were created from the reaction of modified PAN with vanillin PANVan and cinnamaldehyde PANCinn. X-ray diffraction analysis (XRD), Fourier transform infrared (FTIR), Thermogravimetric analysis (TGA), and scanning electron microscopy (SEM) were employed to elucidate the structure of the resultant Schiff bases. Each compound's capability to inhibit bacterial growth and eliminate methylene blue dye (MB) from aqueous solutions was assessed. The fabricated PAN Schiff bases were able to inhibit the bacterial growth of both Gram-negative bacteria with inhibitory zone diameters ranging from 8.5 to 12.3 mm and Gram-positive bacteria with inhibitory zone diameters ranging from 9 to 15.6 mm. Furthermore, 77.8 % of the MB dye was found to be removed by PANVan nanofibers. This dye removal process was discovered to be endothermic, following the Langmuir isotherm model and having pseudo-second-order kinetics as a description. It has been discovered that PANVan nanofibers can be reused for dye removal. Simulated adsorption and docking studies were found to agree with dye removal and antibacterial studies. These synthesized Schiff bases could demonstrate their promise as bactericidal agents and useful materials for environmental applications involving the removal of dyes.

Tröger’s base-derived thin film composite membrane for enhanced nanofiltration performance

Nanofiltration (NF) membrane technology serves as an efficient method for separation and purification, playing a vital role in various industrial fields such as water treatment, food processing, and pharmaceutical manufacturing. However, there are still drawbacks, such as limited flux due to densely crosslinked composite layer and poor stability in solvents. In this study, we report the fabrication of the thin-film composite (TFC) NF membrane using Tröger’s base-derived building block, aiming to manipulate intrinsic pore structures of the as-synthesized ultra-thin composite layer by introducing rigid dihedral units. The interfacial polymerization process is employed to enable the polycondensation of Tröger’s base-based diamine monomer and tri-aldehyde monomer via Schiff base reaction. The effects of monomer concentration, immersion time, interfacial polymerization reaction time, heat treatment time and temperature on the performance of NF membrane were studied. The optimized NF membrane presents a rejection of Methyl blue (MB) above 95.3 % and achieves a high water permeance of 43.4 L·m−2·h−1·bar−1. The water permeance is 2–3 times higher than the reported NF membranes with similar rejection ability. In addition, Tröger’s base-derived TFC NF membrane exhibits excellent long-term stability and good organic solvent tolerance. Considering the high water permeance and separation efficiency, the present membrane has significance in dye removal and separation processes.

Sustainable membrane technology for water purification—Manufacturing, recycling and environmental impacts

Water pollution has become a serious threat to our ecosystem. Water contamination due to human, commercial, and industrial activities has negatively affected the whole world. Owing to the global demanding challenges of water pollution treatments and achieving sustainability, membrane technology has gained increasing research attention. Although numerous membrane materials have focused, the sustainable water purification membranes are most effective for environmental needs. In this regard sustainable, green, and recyclable polymeric and nanocomposite membranes have been developed. Materials fulfilling sustainable environmental demands usually include wide-ranging polyesters, polyamides, polysulfones, and recyclable/biodegradable petroleum polymers plus non-toxic solvents. Consequently, water purification membranes for nanofiltration, microfiltration, reverse osmosis, ultrafiltration, and related filtration processes have been designed. Sustainable polymer membranes for water purification have been manufactured using facile techniques. The resulting membranes have been tested for desalination, dye removal, ion separation, and antibacterial processes for wastewater. Environmental sustainability studies have also pointed towards desired life cycle assessment results for these water purification membranes. Recycling of water treatment membranes have been performed by three major processes mechanical recycling, chemical recycling, or thermal recycling. Moreover, use of sustainable membranes has caused positive environmental impacts for safe waste water treatment. Importantly, worth of sustainable water purification membranes has been analyzed for the environmentally friendly water purification applications. There is vast scope of developing and investigating water purification membranes using countless sustainable polymers, materials, and nanomaterials. Hence, value of sustainable membranes has been analyzed to meet the global demands and challenges to attain future clean water and ecosystem.

Production of Porous Biochar from Cowdung and its Application

Porous activated carbon (PAC) powder is prepared from solid bio-waste - cow dung samples (CD). UV- Spectroscopy confirms the absorption rate of activated porous biochar at different concentration solutions(in ppm).The activation process is carried out by phosphoric acid and sodium hydroxide treatment followed by calcination at different temperature condition. XRD pattern confirms the amorphous phase formation with graphitic nature for different precursor utilization. SEM analysis shows the uniform and hierarchical porous network formation and aggregated particle with tiny. X- ray analysis confirms the formation of graphitic carbon and porous morphology for sample activated at increased calcination temperature. The elemental composition of as prepared carbon samples is determined by SEM and confirms the formation major carbon content existence. The obtained product is observed for the dye removal process wherein the specific amount of PAC is added to the Methylene Blue(MB) dye solutions and the absorption rate is observed through uv-spectroscopy.