Search Results (51)

Aldehyde green, a dye first obtained by reacting fuchsine with acetaldehyde in 1862, consists of, according to analytical investigations carried out on a sample of this dye deposited in the Historical Dyestuff Collection of the Technical University Dresden and performed with liquid chromatography and high-resolution mass spectrometry, a mixture of various compounds in which the aniline groups of fuchsine are converted into quinaldine and dihydroquinaldine moieties. The dye owns its green color by two absorption bands in the visible range at 435 and 616 nm. Full article

This study addresses the dual challenges of water pollution and waste management by exploring the valorization of chicken bone biomass in native (NBio) and calcined (CBio) forms as biosorbents for dye removal. Basic fuchsine (BF) and methylene blue (MB) were selected as model pollutants, and adsorption was assessed under varying operational conditions. Characterization using Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD) showed that calcination improved crystallinity, eliminated organic impurities, and increased surface area (247 m²/g for NBio vs. 370 m²/g for CBio). Adsorption tests revealed higher performance for CBio, with maximum adsorption capacities of 100 mg/g (BF) and 142.85 mg/g (MB) based on the Langmuir isotherm, while NBio with maximum adsorption capacities of 111 mg/g (BF) and 111.11 mg/g (MB) followed the Freundlich model. Adsorption kinetics indicated pseudo-second-order behavior, suggesting chemisorption. The possible interactions between dyes and the biosorbent are hydrogen bonding, electrostatic interactions, and Lewis acid–base interactions. Thermodynamic analysis highlighted exothermic behavior for NBio and endothermic, entropy-driven adsorption for CBio, with both processes being spontaneous. A decision tree with Least Squares Boosting (DT_LSBOOST) provided accurate predictions (R² = 0.9999, RMSE < 0.003) by integrating key parameters. These findings promote chicken bone biomass as a cost-effective, sustainable biosorbent, offering promising potential in wastewater treatment and environmental remediation. Full article

Nanotechnology offers effective solutions for removing contaminants and harmful bacteria from polluted water. This study synthesized copper nanoparticles using a carbohydrate-based bioflocculant derived from Proteus mirabilis AB 932526.1. The bioflocculant is a natural polymer that facilitates the aggregation of particles, enhancing the efficiency of the nanoparticle synthesis process. Characterization of the bioflocculant and copper nanoparticles was conducted using Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, Ultraviolet-Visible Spectroscopy, X-ray Diffraction, and Transmission Electron Microscopy techniques to assess their properties, flocculation efficiency, and antibacterial characteristics. The optimal flocculation efficiency of 80% was achieved at a copper nanoparticle concentration of 0.4 mg/mL, while a concentration of 1 mg/mL resulted in a lower efficiency of 60%. The effects of biosynthesized copper nanoparticles on human-derived embryonic renal cell cultures were also investigated, demonstrating that they are safe at lower concentrations. The copper nanoparticles effectively removed staining dyes such as safranin (90%), carbol fuchsine (88%), methylene blue (91%), methyl orange (93%), and Congo red (94%), compared to a blank showing only 39% removal. Furthermore, when compared to both chemical flocculants and bioflocculants, the biosynthesized copper nanoparticles exhibited significant nutrient removal efficiencies for nitrogen, sulfur, phosphate, and total nitrates in coal mine and Vulindlela domestic wastewater. Notably, these biosynthesized copper nanoparticles demonstrated exceptional antibacterial activity against both Gram-positive and Gram-negative bacteria. Full article

Dialdehyde cellulose fabric (DACF) membranes with varying degrees of oxidation were fabricated using periodate oxidation and were employed for the chemical adsorption of amino-groups containing dyes from wastewater. The aldehyde group contents of DACF membranes were adjusted by altering oxidation time, which was confirmed by titration experiments. The chemical structure and morphology of DACF membranes were characterized using ATR-FTIR, TGA, SCA, SEM, XPS, and XRD measurements. The optimized DACF membrane, which was treated for an oxidation time of 24 h and has an aldehyde content of 2.97 mmol/g, was used for the chemical adsorption of amino-containing dye molecules. This process relies on the Schiff base reaction between the amino groups of the target dye molecule and the aldehyde groups of the membrane. Two typical cationic dyes, fuchsin basic and chrysoidine, containing aromatic amino groups, were chosen to determine the adsorption capacity of the DACF membrane. The adsorption kinetics, isotherms, and thermal dynamics of the DACF membrane were investigated comprehensively, while both pseudo-first- and pseudo-second-order kinetics models fit well, indicating the complicated chemical/diffusion adsorption process, where the hydrophobic properties of the DACF membrane retarded the adsorption rate. The maximum adsorption capacities of the DACF membrane against fuchsin basic and chrysoidine were 108.69 and 46.29 mg/g, respectively, as determined by Langmuir isotherm simulations. Various competing ions such as Na⁺, Ca²⁺, Cl⁻, and SO₄²⁻ at high concentrations of 10,000 ppm were used to challenge the adsorption capability of the DACF membrane, with negligible effects observed. A new adsorption mechanism based on chemical/diffusion interaction was proposed. Bovine serum albumin (BSA), fuchsin basic, and chrysoidine were mixed to simulate the multicomponent wastewater containing dissolved organic nitrogen (DON) and demonstrated the adsorption process; the direct adsorption capacity of the DACF membrane was up to 63.0%. This work offers a new method for the highly efficient removal of organic pollutants by a chemical reaction approach. 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

This study is the first to convert two waste materials, waste rice noodles (WRN) and red mud (RM), into a low-cost, high-value magnetic photocatalytic composite. WRN was processed via a hydrothermal method to produce a solution containing carbon quantum dots (CQDs). Simultaneously, RM was dissolved in acid to form a Fe³⁺ ion-rich solution, which was subsequently mixed with the CQDs solution and underwent hydrothermal treatment. During this process, the Fe³⁺ ions in RM were transformed into the maghemite (γ-Fe₂O₃) phase, while CQDs were incorporated onto the γ-Fe₂O₃ surface, resulting in the CQDs/γ-Fe₂O₃ magnetic photocatalytic composite. Experimental results demonstrated that the WRN-derived CQDs not only facilitated the formation of the magnetic γ-Fe₂O₃ phase but also promoted a synergistic interaction between CQDs and γ-Fe₂O₃, enhancing electron-hole pair separation and boosting the production of reactive radicals such as O₂^·− and ·OH. Under optimized conditions (pH = 8, carbon loading: 10 wt%), the CQDs/γ-Fe₂O₃ composite exhibited good photocatalytic performance against methylene blue, achieving a 97.6% degradation rate within 480 min and a degradation rate constant of 5.99 × 10⁻³ min⁻¹, significantly outperforming RM and commercial γ-Fe₂O₃ powder. Beyond methylene blue, this composite also effectively degraded common organic dyes, including malachite green, methyl violet, basic fuchsin, and rhodamine B, with particularly high efficiency against malachite green, reaching a degradation rate constant of 5.465 × 10⁻² min⁻¹. Additionally, due to its soft magnetic properties (saturation magnetization intensity: 16.7 emu/g, residual magnetization intensity: 2.2 emu/g), the material could be conveniently recovered and reused after photocatalytic cycles. Even after 10 cycles, it retained over 98% recovery and 96% photocatalytic degradation efficiency, underscoring its potential for cost-effective, large-scale photocatalytic water purification. Full article

Carbon dioxide corrosion presents a significant challenge in the oil and gas field. This study simulates the corrosive environment characteristics of oil and gas fields to investigate the corrosion inhibition properties of three triphenylmethane dyes. The inhibitive performance and mechanisms of these dyes were analyzed through weight loss and electrochemical testing, revealing that crystal violet (CV) exhibited a superior inhibition effectiveness over malachite green (MG) and Fuchsine basic (FB). At a concentration of 150 ppm in a CO₂-saturated 5% NaCl solution at 25 °C, CV achieved an impressive maximum inhibition efficiency of 94.89%. With the increase in temperature, the corrosion rate slightly decreased, and the corrosion rate was 92.94% at 60 °C. The investigated CV acted as a mixed-type corrosion inhibitor and its protection obeyed the Langmuir adsorption isotherm. The corrosion morphology was characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and confocal laser scanning microscopy (CLMS). Quantum chemical calculations and molecular dynamics simulations were employed to validate the corrosion inhibition mechanisms, providing guidance for the further application of these dyes in corrosion control. Full article

The utilization of titanium dioxide (TiO₂) as a photocatalyst for the treatment of wastewater has attracted significant attention in the environmental field. Herein, we prepared an NH₂-MIL-125-derived N-doped TiO₂@C Visible Light Catalyst through an in situ calcination method. The nitrogen element in the organic connector was released through calcination, simultaneously doping into the sample, thereby enhancing its spectral response to cover the visible region. The as-prepared N-doped TiO₂@C catalyst exhibited a preserved cage structure even after calcination, thereby alleviating the optical shielding effect and further augmenting its photocatalytic performance by increasing the reaction sites between the catalyst and pollutants. The calcination time of the N-doped TiO₂@C-450 °C catalyst was optimized to achieve a balance between the TiO₂ content and nitrogen doping level, ensuring efficient degradation rates for basic fuchsin (99.7%), Rhodamine B (89.9%) and tetracycline hydrochloride (93%) within 90 min. Thus, this study presents a feasible strategy for the efficient degradation of pollutants under visible light. Full article

Both the endocannabinoid system (ECS) and estrogens have significant roles in cardiovascular control processes. Cannabinoid type 1 receptors (CB₁Rs) mediate acute vasodilator and hypotensive effects, although their role in cardiovascular pathological conditions is still controversial. Estrogens exert cardiovascular protection in females. We aimed to study the impact of ECS on vascular functions. Experiments were performed on CB₁R knockout (CB₁R KO) and wild-type (WT) female mice. Plasma estrogen metabolite levels were determined. Abdominal aortas were isolated for myography and histology. Vascular effects of phenylephrine (Phe), angiotensin II, acetylcholine (Ach) and estradiol (E2) were obtained and repeated with inhibitors of nitric oxide synthase (NOS, Nω-nitro-L-arginine) and of cyclooxygenase (COX, indomethacin). Histological stainings (hematoxylin-eosin, resorcin-fuchsin) and immunostainings for endothelial NOS (eNOS), COX-2, estrogen receptors (ER-α, ER-β) were performed. Conjugated E2 levels were higher in CB₁R KO compared to WT mice. Vasorelaxation responses to Ach and E2 were increased in CB₁R KO mice, attenuated by NOS-inhibition. COX-inhibition decreased Phe-contractions, while it increased Ach-relaxation in the WT group but not in the CB₁R KO. Effects of indomethacin on E2-relaxation in CB₁R KO became opposite to that observed in WT. Histology revealed lower intima/media thickness and COX-2 density, higher eNOS and lower ER-β density in CB₁R KO than in WT mice. CB₁R KO female mice are characterized by increased vasorelaxation associated with increased utilization of endothelial NO and a decreased impact of constrictor prostanoids. Our results indicate that the absence or inhibition of CB₁Rs may have beneficial vascular effects. Full article

Recently, there has been an active search for new modifiers to create hybrid polymeric materials for various applications, in particular, membrane technology. One of the topical modifiers is metal-organic frameworks (MOFs), which can significantly alter the characteristics of obtained mixed matrix membranes (MMMs). In this work, new holmium-based MOFs (Ho-MOFs) were synthesized for polyether block amide (PEBA) modification to develop novel MMMs with improved properties. The study of Ho-MOFs, polymers and membranes was carried out by methods of X-ray phase analysis, scanning electron and atomic force microscopies, Fourier transform infrared spectroscopy, low-temperature nitrogen adsorption, dynamic and kinematic viscosity, static and dynamic light scattering, gel permeation chromatography, thermogravimetric analysis and contact angle measurements. Synthesized Ho-MOFs had different X-ray structures, particle forms and sizes depending on the ligand used. To study the effect of Ho-MOF modifier on membrane transport properties, PEBA/Ho-MOFs membrane retention capacity was evaluated in vacuum fourth-stage filtration for dye removal (Congo Red, Fuchsin, Glycine thymol blue, Methylene blue, Eriochrome Black T). Modified membranes demonstrated improved flux and rejection coefficients for dyes containing amino groups: Congo Red, Fuchsin (PEBA/Ho-1,3,5-H₃btc membrane possessed optimal properties: 81% and 68% rejection coefficients for Congo Red and Fuchsin filtration, respectively, and 0.7 L/(m²s) flux). Full article

In this work, amorphous and crystalline novel products based on Zr, Mg, and Mn were facilely fabricated through the Pechini sol–gel procedure using inexpensive chemicals and an uncomplicated apparatus. Also, these products showed high efficiency as novel adsorbents in getting rid of basic fuchsin dye from aqueous solutions. The adsorbent, which was fabricated before calcination, was abbreviated as KE. In addition, the adsorbents, which were created at 500 and 700 °C, were designated as KE500 and KE700, respectively. The created adsorbents were characterized using high-level transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), N₂ adsorption/desorption analyzer, and field emission scanning electron microscope (FE-SEM). The XRD showed that the KE adsorbent is amorphous, whereas the KE500 and KE700 adsorbents are mixtures of ZrO₂, MgMn₂O₄, and Mg(Mg_0.333Mn_1.333)O₄ nanostructures. The HR-TEM exhibited that the KE adsorbent consists of very fine irregular shapes, whereas the KE500 adsorbent contains quasi-spherical particles with a mean diameter of 45.16 nm. Furthermore, the HR-TEM exhibited that the KE700 adsorbent consists of polyhedral shapes with a mean diameter of 76.28 nm. Furthermore, the BET surface area of the KE, KE500, and KE700 adsorbents is 67.85, 20.15, and 13.60 m²/g, respectively. Additionally, the elimination of basic fuchsin dye by the KE, KE500, and KE700 adsorbents is exothermic, physical in nature, and follows the pseudo-first-order as well as Langmuir equations. Further, the maximum uptake capabilities of the KE, KE500, and KE700 adsorbents toward basic fuchsin dye are 239.81, 174.83, and 93.19 mg/g, respectively. Full article

ZnO is an effective photocatalyst applied to the degradation of organic dyes in aqueous media. In this study, the UV-light and sunlight-driven photocatalytic activities of ZnO nanoparticles are evaluated. A handheld Lovibond photometer was purposefully calibrated in order to monitor the dye removal in outdoor conditions. The effect of ZnO defect states, i.e., the presence of zinc and oxygen defects on the photocatalytic activity was probed for two types of dyes: fuchsin and methylene blue. Three morphologies of ZnO nanoparticles were deliberately selected, i.e., spherical, facetted and a mix of spherical and facetted, ascertained via transmission electron microscopy. Aqueous and non-aqueous sol-gel routes were applied to their synthesis in order to tailor their size, morphology and defect states. Raman spectroscopy demonstrated that the spherical nanoparticles contained a high amount of oxygen vacancies and zinc interstitials. Photoluminescence spectroscopy revealed that the facetted nanoparticles harbored zinc vacancies in addition to oxygen vacancies. A mechanism for dye degradation based on the possible surface defects in facetted nanoparticles is proposed in this work. The reusability of these nanoparticles for five cycles of dye degradation was also analyzed. More specifically, facetted ZnO nanoparticles tend to exhibit higher efficiencies and reusability than spherical nanoparticles. Full article

There are two types of secretory cells in the chicken bursa of Fabricius (BF): (a) interfollicular epithelial cells (IFE), and (b) bursal secretory dendritic cells (BSDC) in the medulla of bursal follicles. Both cells produce secretory granules, and the cells are highly susceptible to IBDV vaccination and infection. Before and during embryonic follicular bud formation, an electron-dense, scarlet-acid fuchsin positive substance emerges in the bursal lumen, the role of which is unknown. In IFE cells, IBDV infection may induce rapid granular discharge, and in several cells, peculiar granule formation, which suggests that the glycosylation of protein is injured in the Golgi complex. In control birds, the discharged BSDC granules appear in membrane-bound and subsequently solubilized, fine-flocculated forms. The solubilized, fine-flocculated substance is Movat-positive and can be a component of the medullary microenvironment, which prevents the medullary B lymphocytes from nascent apoptosis. Vaccination interferes with the solubilization of the membrane-bound substance, resulting in: (i) aggregation of a secreted substance around the BSDC, and (ii) solid lumps in the depleted medulla. The non-solubilized substance is possibly not “available” for B lymphocytes, resulting in apoptosis and immunosuppression. In IBDV infection, one part of the Movat-positive Mals fuse together to form a medullary, gp-containing “cyst”. The other part of Mals migrate into the cortex, recruiting granulocytes and initiating inflammation. During recovery the Movat-positive substance appears as solid, extracellular lumps between the cells of FAE and Mals. Possibly the Mals and Movat-positive extracellular lumps glide into the bursal lumen via FAE to eliminate cell detritus from the medulla. Full article

This work aims to prepare and characterize the unburned carbon obtained from gasification residues and evaluate its application as an adsorbent for the removal of textile dye contaminants. The results of physical and chemical properties showed a specific mass of 2.05 g/cm³, surface area of 23.983 g/cm², and diameter and pore volume of 0.844 nm and 2.262 cm³/g, respectively. These properties, along with the point of zero charge and chemical bonds present on the surface, favored the adsorption of cationic dyes. The adsorption results showed great potential for the removal of methylene blue, crystal violet, and basic fuchsin if compared with bromocresol green, and indigo carmine. The maximum removal values obtained for methylene blue were up to 99% and the kinetic adsorption was faster at the beginning of the process, reaching the equilibrium in less than 5 min. The results obtained through the adsorption isotherms showed a maximum adsorption capacity of 333.33 and 476.19 mg/g, at the temperature of 291 and 328 K, respectively. The satisfactory results showed that the use of unburned carbon is a cost-effective and eco-friendly alternative to reusing the residue from gasification and also contributes to the decontamination of watercourses. Full article

This research examined the production of a V₂O₅-g-C₃N₄ nanocomposite to remove organic dyes from wastewater. To generate the V₂O₅-g-C₃N₄ nanocomposite, the sonication method was applied. The testing of V₂O₅-g-C₃N₄ with various dyes (basic fuchsin (BF), malachite green (MG), crystal violet (CV), Congo red (CR), and methyl orange (MO)) revealed that the nanocomposite has a high adsorption ability towards BF, MG, CV, and CR dyes in comparison with MO dye. It was established that the modification of pH influenced the removal of CV by the V₂O₅-g-C₃N₄ nanocomposite and that under optimal operating conditions, efficiency of 664.65 mg g⁻¹ could be attained. The best models for CV adsorption onto the V₂O₅-g-C₃N₄ nanocomposite were found to be those based on pseudo-second-order adsorption kinetics and the Langmuir isotherm. According to the FTIR analysis results, the CV adsorption mechanism was connected to π–π interactions and the hydrogen bond. Full article