Search Results (19)

In this study, polyethersulfone (PES)/sulfonated polyethersulfone (SPES) composite nanofiltration membranes doped with different contents of monolayer titanium carbide nanosheets (Ti₃C₂T_X) were prepared by the nonsolvent induced phase inversion (NIPS) method. The effects of Ti₃C₂T_X on membrane structure, separation performance and antibacterial activity were investigated systematically. The results demonstrated that the viscosity of the casting solution increased significantly with the increasing content of Ti₃C₂T_X. In addition, the pore size of the membrane surface first decreased and then increased; porosity and hydrophilicity were optimized synchronously; and the density of negative charges on the surface increased. The M2 membrane showed a rejection rate of more than 90% for Metanil yellow (MY) and methylene blue (MEB). The order of salt ion rejection rates was magnesium sulfate (MgSO₄) > sodium sulfate (Na₂SO₄) > sodium chloride (NaCl), and water flux reached the peak (18.5 L/m²·h·bar). The antibacterial activity of the M2 membrane was significantly enhanced, and its antibacterial rate against Bacillus subtilis increased from 15% (M0) to 58%. This phenomenon was attributed to the synergistic mechanism of the Ti₃C₂T_X physical capture effect, reactive oxygen species (ROS) generation and sharp edge damage to bacterial cell membranes. This study provides theoretical support and a technical path for the development of MXene composite membranes with high separation efficiency and excellent antibacterial properties. Full article

The dyes used to produce two Palestinian garments from the British Museum’s collection attributed to the late 19th–early 20th century were investigated by high pressure liquid chromatography coupled with diode array detector and tandem mass spectrometry (HPLC-DAD-MS/MS). Palestinian embroidery is a symbol of national identity and the topic of scholarly research. However, little attention has been given to the dyes and how these changed with the introduction of new synthetic formulations in the second half of the 19th century. The results revealed the use of natural indigoid blue and red madder (Rubia tinctorum), in combination with tannins. Yellow from buckthorn (probably Rhamnus saxatilis) and red from cochineal (probably Dactylopius coccus) were found mixed with synthetic dyes in green and dark red embroidery threads, respectively. Early synthetic dyes were identified in all the other colours. These include Rhodamine B (C.I. 45170), Orange II (C.I. 15510), Orange IV (C.I. 13080), Metanil Yellow (C.I. 13065), Chrysoidine R (C.I. 11320), Methyl Violet (C.I. 42535), Malachite Green (C.I. 42000), Fuchsin (C.I. 42510), Auramine O (C.I. 41000) and Methyl Blue (C.I. 42780). As the date of the first synthesis of these dyes is known, the production date of the garments was refined, suggesting that these were likely to be produced towards the end of the 1880s/beginning of the 1890s. The continuous use of historical local sources of natural dyes, alongside new synthetic dyes, is of particular interest, adding rightful nuances to the development of textile-making practices in this region. Full article

Excessive water hyacinth growth in aquatic environments and metanil yellow (MY) dye in industrial wastewater pose severe environmental and public health challenges. Therefore, this study evaluated the effects of various process factors on batch MY biosorption onto water hyacinth leaves (LECs) and MY biosorption kinetics, equilibrium, and thermodynamics. The optimal pH for MY biosorption by LECs was 1.5–2.0. The initial MY concentration affected the equilibrium MY biosorption capacity but not the LEC particle size and solution temperature. However, the LEC particle size and solution temperature affected the MY biosorption rate; the biosorption rate was higher at a lower particle size (0.15–0.3 mm) and a higher temperature (62 °C) than at higher particle sizes and lower temperatures. The pseudo-second-order model adequately described the biosorption kinetics of MY by LECs at the different levels of the process factors, whereas the Sips and Redlich–Peterson models satisfactorily represented the biosorption isotherm of MY. The Sips model predicted a maximum MY biosorption capacity of 170.8 mg g⁻¹. The biosorption of MY by LECs was endothermic and not spontaneous. These findings demonstrate that LECs exhibit great potential for bioremediating MY-contaminated wastewater, thereby providing valuable insights for effective water treatment and pollution control strategies. Full article

This study explores the detailed characterization of a biosorbent (Hen Feather) and its efficient use in eradicating the azo dye Metanil Yellow (MY) from its aqueous solutions. Effects of a range of experimental parameters, including pH, initial dye concentration, biosorbent dosage and contact time on the adsorption, were studied. A detailed physical and chemical characterization of the biosorbent was made using SEM, XRD, XPS and FTIR. During the optimization of adsorption parameters, the highest dye uptake of almost 99% was recorded at pH 2, dye concentration 2 × 10⁻⁵ M, 0.05 g of biosorbent and a contact period of 75 min. Various adsorption isotherm models were studied to gather different adsorption and thermodynamic parameters. The linearity of the Langmuir, Freundlich and D-R adsorption isotherms indicate homogeneous, multilayer chemisorption with high adsorption affinity between the dye and biosorbent. Values of the changes in the Gibbs free energy (ΔG°) and the enthalpy (ΔH°) of the adsorption process have been calculated, these values indicate that it is a spontaneous and endothermic process. Kinetics of the adsorption were also measured, and it was established that the adsorption of MY over Hen Feather follows a pseudo-second-order kinetic model at temperatures 30, 40 and 50 °C. The findings of this investigation clearly indicate that the studied biosorbent exhibits a high affinity towards the dye (MY), and it can be effectively, economically and efficiently used to sequestrate and eradicate MY from its aqueous solutions. Full article

This study reports on the highly simple fabrication of green carbon black (GCB) generated from scrap tires with acetic acid to improve the adsorption efficiency for water purification, which is thoroughly compared with conventional carbon black (CB) obtained from petrochemicals. Unlike traditional modification processes with strong acids or bases, the introduction of a relatively mild acid readily allowed for the effective modification of GCB to increase the uptake capability of metal ions and toxic organic dyes to serve as effective adsorbents. The morphological features and thermal decomposition patterns were examined by electron microscopy and thermogravimetric analysis (TGA). The surface functional groups were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The structural information (ratio of D-defects/G band-graphitic domains) obtained by Raman spectroscopy clearly suggested the successful fabrication of GCB (I_D/I_G ratio of 0.74), which was distinctively different from typical CB (I_D/I_G ratio of 0.91). In the modified GCB, the specific surface area (S_BET) gradually increased with the reduction of pore size as a function of acetic acid content (52.97 m²/g for CB, 86.64 m²/g for GCB, 102.10-119.50 m²/g for acid-treated GCB). The uptake capability of the modified GCB (312.5 mg/g) for metal ions and organic dyes was greater than that of the unmodified GCB (161.3 mg/g) and typical CB (181.8 mg/g), presumably due to the presence of adsorbed acid. Upon testing them as adsorbents in an aqueous solution, all these carbon materials followed the Langmuir isotherm over the Freundlich model. In addition, the removal rates of cationic species (>70% removal of Cu²⁺ and crystal violet in 30 min) were much faster and far greater than those of anionic metanil yellow (<40% removal in 3 h), given the strong electrostatic interactions. Thus, this work demonstrates the possibility of recycling waste tires in the powder form of GCB as a cost-effective and green adsorbent that can potentially substitute traditional CB, and the modification strategy provides a proof of concept for developing simple fabrication guidelines of other carbonaceous materials. Full article

We investigate the possibility of modification of SnS₂ powder through sonochemical synthesis with the addition of an organic ligand. For that purpose, two organic dyes are used, Phenol Red and Anthraquinone Violet. All obtained powders are characterized using XRD, SEM, EDX, FT-IR, and UV-Vis investigations. Synthesized samples showed composition and structural properties typical for sonochemically synthesized SnS₂. However, investigation with the Tauc method revealed that SnS₂ powder modified with Phenol Red exhibits a significant shift in value of optical bandgap to 2.56 eV, while unmodified SnS₂ shows an optical bandgap value of 2.42 eV. The modification of SnS₂ powder with Anthraquinone Violet was unsuccessful. The obtained nanopowders were utilized as photocatalysts in the process of Metanil Yellow degradation, revealing that SnS₂ modified with Phenol Red shows about 23% better performance than the unmodified one. The mean sonochemical efficiency of the performed synthesis is also estimated as 9.35 µg/W. Full article

The cost-effective adsorbents of carbonized pistachio shell magnetic nanoparticles (CPSMNPs) were synthesized. SEM, EDX, and BET characterized the prepared CPSMNPs. The CPSMNPs were used as adsorbents to remove Metanil Yellow (MY) dye. The adsorption of MY was investigated with the effect of pH, contact time, initial dye concentration, adsorbent dose, and temperature. The SEM image of CPSMNPs reveals fine particles with an average size of 400–700 nm and a substantial surface area increase (112.58 m²/g). The EDX analysis confirms the carbonization of PS to CPS and the successful impregnation of Fe₃O₄ nanoparticles. CPSMNPs showed excellent adsorption efficiency, i.e., 94% for adsorption of MY of 10 mL of 100 ppm MY at optimum conditions. Kinetics data fit pseudo-second-order kinetics. The Langmuir isotherm better represents the equilibrium data with the spontaneous sorption process. This study investigates that the synthesized nanoparticles have an excellent texture and can be used as a special adsorbent for the adsorption of wastewater pollutants like MY. Full article

This work provides an alternative method for evaluating the photodegradation behaviour of different types of dyes such as Methylene Blue, Rhodamine B, Congo Red, Metanil Yellow, and Malachite Green. In this methodology, the coating is dyed with the chosen colorant and two beams of light are combined and channelled to a spot on the dyed coating through an optical fibre, the first one from an ultraviolet (UV) source (which is the responsible of activating photocatalysis) and the second one from a Visible light source, which is employed to monitor changes in colour along the time. The photocatalytic coating selected for testing this methodology consists of a mat of electrospun poly (acrylic acid) (PAA) fibres that acts as base film, furtherly coated by using layer-by-layer (LbL) assembly technique for the immobilization of two different photocatalytic metal oxide precursors (TiO₂ and Fe₂O₃) nanoparticles. The morphological characterization of the samples has been implemented by means of scanning electron microscopy (SEM), confocal microscopy, and water contact angle measurements in order to analyse the resultant thickness, roughness, electrospun fibre diameter, and wettability. The experimental results clearly demonstrate the validity of the methodology to measure the photocatalytic activity in all dyed coatings, although significant differences have been observed depending on the selected dye. Full article

The present manuscript explores a spectroscopic technique to select turmeric powder, free from impurities, and has compounds of medicinal importance among the tainted and natural turmeric. Six Curcuma longa (turmeric powder) samples, named S1, S2, S3, S4, S5, and S6, were analyzed to discriminate between tainted and natural turmeric using the LIBS and multivariate technique. Other techniques such as UV–Vis, FTIR, and EDX are also used to ascertain the elements/compounds showing the medicinal properties of C. longa. Spectral lines of carbon, sodium, potassium, magnesium, calcium, iron, strontium, barium, and electronic bands of CN molecules were observed in the LIBS spectra of turmeric samples. Spectral signatures of toxic elements such as lead and chromium are also observed in the LIBS spectra of all samples except S6. Adulteration of metanil yellow, a toxic azo dye, is used to increase the appearance of curcumin when the actual curcumin content is low. The presence of spectral lines of lead and chromium in the LIBS spectra of S1 to S5 suggested that it may be adulterated with lead chromate which is used for coloring turmeric. Further, the presence of sulfur in EDX analysis of sample S5 indicates that it may also have been adulterated with metanil (C₁₈H₁₄N₃NaO₃S). The concentration of samples’ constituents was evaluated using CF-LIBS, and EDX was used to verify the results obtained by CF-LIBS. The principal component analysis applied to the LIBS data of the turmeric samples has been used for instant discrimination between the sample based on their constituents. We also analyzed antioxidant activity and total phenolic and flavonoid content of different turmeric samples and found a negative Pearson correlation with heavy metals. The presence of curcumin in turmeric is confirmed using LIBS and UV–Vis, which have medicinal properties. Full article

The present work aims to provide insight into the role of the functional group in the adsorption of azo dyes namely, ethyl orange (EO), methyl orange (MO), and metanil yellow (MY), on the activated carbon (surface area 569 m²·g⁻¹) prepared from Phyllanthus emblica fruit stone by low-pressure hydrothermal treatment (AC-HTPEFS). More specifically, this study would facilitate a better understanding of the involvement of different amino substituents (-CH₃, -C₂H₅, phenyl group) on the adsorption of azo dye molecules. The experimental adsorption isotherms of the azo dyes quantified with different adsorbents and temperatures (25–45 °C) were utilized to know the effect of functional groups on dye adsorption. Additionally, the equilibrium data were analyzed by applying isotherm models (Freundlich, Langmuir, and Temkin) in order to elucidate the best-fit isotherm model and adsorption capacity, with the Langmuir model fitting the isotherms best as shown by the higher correlation coefficients obtained (0.984–0.994). The Langmuir monolayer adsorption capacities of EO, MO, and MY obtained at 25 °C were found to be 0.202, 0.187, and 0.158 mmol·g⁻¹, respectively, which was attributed to the hydrophobicity and geometry of dye molecules. Moreover, adsorption kinetics conformed well with the pseudo-second-order model. The negative ΔG°, positive ΔH,° and positive ΔS° indicated the adsorption process to be favorable, endothermic, and increased randomness at the solid–liquid interface. Our findings indicate that the porous activated carbon from hydrothermally treated Phyllanthus emblica fruit stone exhibited a promising potential for the removal of azo dyes with rapid kinetics and high adsorption capacity. The present study could thus pave a way for future utilization of activated carbons produced via hydrothermal treatment techniques for wastewater applications. Full article

In this work, ZnO nanocrystals (NCs) have been effectively synthesized by a simple, efficient and cost-effective method using coconut husk extract as a novel fuel. The synthesized NCs are characterized by UV-Vis, XRD, FT-IR, SEM, EDX, Raman and PL studies. The obtained ZnO were found to be UV-active with a bandgap of 2.93 eV. The X-ray diffraction pattern confirms the crystallinity of the ZnO with hexagonally structured ZnO with a crystallite size of 48 nm, while the SEM analysis reveals the hexagonal bipyramid morphology. Photocatalytic activities of the synthesized ZnO NCs are used to degrade methylene blue and metanil yellow dyes. Full article

Various synthetic dyes are artificially added to herbal medicines for the purpose of visual attraction. In order to monitor the illegal usage of synthetic dyes in herbal medication, a rapid and straightforward analysis method to determine synthetic dyes is required. The study aimed to develop and validate a high-performance liquid chromatography (HPLC) analysis to determine ten synthetic dyes in Hawthorn fruit, Cornus fruit, and Schisandra fruit. Ten synthetic dyes such as Tartrazine, Sunset yellow, Metanil yellow, Auramine O, Amaranth, Orange II, Acid red 73, Amaranth, New Coccine, Azorubine, and Erythrosine B, were extracted using 50 mM ammonium acetate in 70% MeOH; then separated by gradient elution with a mobile phase consisting of acetonitrile and 50 mM ammonium acetate in distilled water using a photodiode array detector (PDA) at 428 nm or 500 nm. In addition, this study established the LC-MS/MS method to confirm the existence of synthetic dyes in the positive sample solution. The HPLC analysis had good linearity (r² > 0.999). The recoveries of this method ranged from 74.6~132.1%, and the relative standard deviation (RSD) values were less than 6.9%. Most of the samples fulfilled the acceptance criteria of the AOAC guideline. This study demonstrates that the HPLC analysis can be applied to determine ten synthetic dyes in herbal medication. Full article

In the present study, a mixed culture from a local agricultural soil sample was isolated for Metanil Yellow (MY) dye decolorization. The metagenomic analysis confirmed that 42.6% has been dominated by genus Bacillus, while Acinetobacter (14.0%) is present in the microbial communities of the mixed culture. For fungi diversity analysis, around 97.0% was “unclassified” fungi and 3% was Candida. The preliminary investigation in minimal salt media (MSM) showed that 100% decolorization was achieved after 24 h of incubation. Response surface methodology (RSM) was successfully applied using Box-Behnken design (BBD) to study the effect of four independent parameters—MY dye concentration, glucose concentration, ammonium sulfate concentration, and pH—on MY dye decolorization by the mixed bacterial culture. The optimal conditions predicted by the desirability function were 73 mg/L of MY, 1.934% glucose, 0.433 g/L of ammonium sulfate, and a pH of 7.097, with 97.551% decolorization The correlation coefficients (R² and R² adj) of 0.913 and 0.825 indicate that the established model is suitable to predict the effectiveness of dye decolorization under the investigated condition. The MY decolorization of the mixed bacterial culture was not affected by the addition of heavy metals in the growth media. Among the 10 heavy metals tested, only copper gave 56.19% MY decolorization, whereas the others gave almost 100% decolorization. The decolorization potential of the mixed bacterial culture indicates that it could be effective for future bioremediation of soil-contaminated sites and treatment solutions of water bodies polluted with the MY dye. Full article

In this study, the Metanil Yellow (MY) decolorizing mixed culture, namely FN3, has been isolated from agriculture soil. The mixed culture was immobilized using gellan gum. In order to optimize the immobilization process for maximal dye decolorization, Response Surface Methodology (RSM) was performed. The optimal conditions for immobilization predicted by desirability function are 130 mg/L of MY dye concentration, 1.478% of gellan gum concentration, 50 beads and 0.6 cm of beads size with the percentage of decolorization of 90.378%. The correlation coefficients of the model (R² and R² adj) are 0.9767 and 0.9533, respectively. This indicates that the established model is suitable to predict the effectiveness of dye decolorization under the investigated condition. The immobilized beads of mixed culture FN3 were able to be reused up to 15 batches of decolorization. The immobilized cells also have high tolerance towards heavy metals. This was proven by higher dye decolorization rate by the immobilized cells even with the addition of heavy metals in the media. The decolorization potential of the mixed culture indicates that it could be useful for future bioremediation of soil contaminated sites and treatment solutions of water bodies polluted with MY dye. Full article

The photo-induced reactivity of compounds at the surface of photocatalytic materials is used to maintain the cleanliness of the surface of glass, concretes and paints. A standard method to quantify the photocatalytic self-cleaning (SC) properties of non-transparent materials was recently published. It is based on the covering of the sample surface with a defined amount of dye and on the evaluation of the reflectance spectra of the coloured surface under irradiation. The calibration of the spectral changes allowed the quantification of the surface residual dye and the evaluation of the self-cleaning kinetics. The method was tested on seven white and coloured photocatalytic materials using methylene blue (MB), rhodamine B (RhB) and metanil yellow (MY). The main by-products of the MB photocatalytic degradation at the solid/solid interface were identified, showing that MB degradation in solution follows a path quite different from that at the solid/solid interface. Also MY showed a different order of photoreactivity. Furthermore, experiments at the solid/solid interface are more trustworthy than tests in solution for evaluating the self-cleaning ability. The differences of the photocatalytic phenomena at the solid/solid interface in comparison with the most studied photoactivated processes at the solid/liquid interface are outlined. Furthermore, photocatalytic materials showed selectivity toward some specific dyes. This encourages the use of more than one dye for the evaluation of the self-cleaning ability of a photocatalytic material. Full article