Search Results (41)

Wastewater containing triphenylmethane dyes such as malachite green (MG), discharged by textile and food industries, poses significant carcinogenic risks and ecological hazards. Conventional physical adsorption methods fail to degrade these pollutants effectively. To address this challenge, we focused on two-dimensional SnSe₂ semiconductor materials. While their narrow bandgap and unique structure confer exceptional optoelectronic properties, prior research has predominantly emphasized heterojunction systems. We synthesized SnSe₂ with well-defined hexagonal plate-like structures via a one-step hydrothermal method by precisely controlling precursor ratios (Sn:Se = 1:2) and reaction temperatures (120–240 °C). Systematic investigations revealed that hydrothermal temperature modulates the van der Waals forces between crystal planes, enabling selective exposure of (001) and (011) facets, as confirmed by XRD, SEM, and XPS analyses, thereby influencing the exposure of specific crystal facets. Experiments demonstrated that pure SnSe₂ synthesized at 150 °C achieved complete degradation of MG (40 mg/L) within 60 min under visible light irradiation, exhibiting a reaction rate constant (k) of 0.099 min⁻¹. By regulating the exposure ratio of the active (001)/(011) facets, we demonstrate that crystal facet engineering directly optimizes carrier separation efficiency, thereby substantially enhancing the catalytic performance of standalone SnSe₂. This work proposes a novel strategy for designing noble-metal-free, high-efficiency standalone photocatalysts, providing crystal facet-dependent mechanistic insights for the targeted degradation of industrial dyes. Full article

Herein, a heterogeneous Fenton-like catalyst was designed by immobilizing iron oxide (FeS) and nickel sulfide (NiS) on the surface of β-cyclodextrin (β-CD), creating a NiS/FeS@β-CD composite for degrading triphenylmethane cresol red dye. Varied instruments were used to study the physical and chemical characteristics of the NiS/FeS@β-CD catalyst. The appropriate catalytic conditions of the Fenton-like degradation of cresol red by NiS/FeS@β-CD were identified, clarifying that the higher degradation % fulfilled 99.86% with an adsorption % of 27.44% at a cresol red concentration = 50 mg/L, NiS/FeS@β-CD dose = 0.01 g, pH = 3, processing temperature = 30 °C, H₂O₂ concentration = 100 mg/L, and H₂O₂ volume = 1 mL. The kinetic assessments depicted the preference of the second order to represent the Fenton-like degradation of cresol red by NiS/FeS@β-CD. The mechanistic proposition of the adsorption/Fenton-like degradation of cresol red was understood using a quenching test and XPS analysis. Finally, to confirm the durability of NiS/FeS@β-CD, a reusability test was proceeded on the catalyst for five adsorption/Fenton-like degradation runs, with identifying the leaching concentrations of nickel and iron from the catalyst by ICP-OES after each run. Full article

Transparent polymers are key materials for producing a broad category of optical components. For specific uses, the material needs additional adaptation of its basic properties. In this context, the current article is focused on applying two kinds of treatments for tailoring the optical and morphological features of low-density polyethylene to match the criteria as optical retardation plates or band-pass filters. The first kind of treatment involves combined mechanical stretching (at various degrees) and abrasion. The second type of treatment resides in polymer foil exposure to plasma and immersion in a solution of a triphenylmethane derivative. For optical compensation purposes, the polymer foils were subjected to combined mechanical treatments consisting of stretching (at various degrees) and abrasion. To assess the level of produced molecular ordering, the polyethylene films were subjected to polarized infrared spectral measurements, polarized refractometry tests and morphological analyses by polarized light microscopy and atomic force microscopy. The results indicated that inducing birefringence and morphology anisotropy of samples leads to proper optical retardation. For optical filter purposes, the dyed polymer was shown to have changes in colorimetric parameters and morphological features and absorbed radiation in the interval of 480–660 nm, while others were transmitted. These characteristics are adequate for band-pass filter uses. Full article

Dye wastewater pollution, particularly from persistent and toxic polycyclic organic pollutants, such as aniline blue, poses a significant environmental challenge. Aniline blue, a triphenylmethane dye widely used in the textile, leather, paper, and pharmaceutical industries, is notoriously difficult to treat owing to its complex structure and potential for bioaccumulation. In this study, we explored the capacity of Comamonas testosteroni (CT1) to efficiently degrade aniline blue, focusing on the underlying enzymatic mechanisms and degradation pathways. Through prokaryotic transcriptome analysis, we identified a significantly upregulated short-chain dehydrogenase (SDRz) gene (log₂FC = 2.11, p < 0.05) that plays a crucial role in the degradation process. The SDRz enzyme possessed highly conserved motifs and a typical short-chain dehydrogenase structure. Functional validation using an SDRz-knockout strain (CT-ΔSDRz) and an SDRz-expressioning strains (E-SDRz) confirmed that SDRz is essential for aniline blue degradation. The knockout strain CT-ΔSDRz exhibited a 1.27-fold reduction in the degradation efficiency, compared to CT1 strain after 12 h; while the expression strain E-SDRz showed a 1.24-fold increase compared to Escherichia coli DH5α after 12 h. Recombinant SDRz (rSDRz) was successfully produced, showing significant enzymatic activity (1.267 ± 0.04 mmol·L⁻¹·min⁻¹ protein), with kinetic parameters Vmax = 2.870 ± 0.0156 mmol·L⁻¹·min⁻¹ protein and Km = 1.805 ± 0.0128 mM·mL⁻¹. Under optimal conditions, the rSDRz achieved a degradation efficiency of 62.17% for aniline blue. Gas chromatography–mass spectrometry (GC-MS) analysis identified several intermediate metabolites in the degradation pathway, including benzeneacetaldehyde, a, a-diphenyl, 2-amino-4-methylbenzophenone, benzene, 1-dimethylamino-4-phenylmethyl, benzenesulfonic acid, methyl ester, further elucidating the biodegradation mechanism. These findings highlight SDRz as a critical enzyme in the biodegradation of aniline blue, offering valuable insights and a robust theoretical foundation for developing advanced bioremediation strategies to address dye wastewater pollution. Full article

Analysis of the structure of two-domain laccase ScaSL from Streptomyces carpinensis VKM Ac-1300 (with a middle-redox potential) revealed determinants that could affect the increased potential of ScaSL. Site-directed mutagenesis of the ScaSL laccase was carried out, and mutants H286A, H286T, H286W, and F232Y/F233Y were obtained. Replacement of His 286 with Ala led to a decrease in redox potential (0.45 V) and an increase in stability at pH 9 and 11; replacement with Thr led to an increase in redox potential (0.51 V) but to a decrease in the thermal stability of the protein; replacement with Trp did not affect the enzyme properties. Replacement of Phe residues 232 and 233 with Tyr led to a shift in enzyme activity to the acidic pH range without changing the redox potential and a decrease in the thermostability and pH stability of the enzyme. All mutants more efficiently oxidized phenolic substrate 2,6-DMP and were able to participate in direct electron transfer (DET) with MWCNT-modified electrodes. The F232Y/F233/Y mutant was unable to degrade triphenylmethane dyes without a mediator but showed a greater degree of decolorization of azo dyes in the presence of the mediator. The crystal structure of laccase with the highest potential was determined with high resolution. Full article

This research focuses on analyzing wool samples dyed with synthetic dyes from the early 20th century. A methodology to identify and distinguish wool fibers dyed with azo, triphenylmethane, and xanthene dyes, which are no longer in use, using the ATR-FTIR spectra, is presented. Firstly, the dataset was subjected to PCA, which revealed the similarities and differences among the samples, illustrating a distribution pattern based on dye classes. MCR-ALS was employed to extract the spectral profiles of the dyed fibers, thereby enhancing the efficacy of the analytical techniques and extracting the comprehensive information from a single instrument. The combination of ATR-FTIR spectroscopy with chemometric methods, such as PCA and MCR-ALS, has proven to be an effective strategy for identifying and differentiating wool fibers dyed with early azo, triphenylmethane, and xanthene dyes. This approach has demonstrated particular effectiveness in enabling rapid analysis without requiring sampling or pretreatment. Moreover, the analysis is supported by thorough bibliographic research on these no longer used colorants. In order to maximize the potential of non-destructive spectroscopic techniques, such as ATR-FTIR, the approach used has proven to be crucial. This study underscores how chemometric techniques expand the capabilities of spectroscopy, extracting extensive information from a single instrument and aligning with the goals of cultural heritage analysis. Full article

A nanostructured material, ordered mesoporous carbon (OMC), was synthesised in metal- and halide-free form and its use for the sequestration of crystal violet, a hazardous triphenylmethane dye, is reported for the first time. The OMC material is characterised using scanning transmission electron microscopy with energy-dispersive spectroscopy for chemical analysis, by Fourier-transform infrared spectroscopy, and by nitrogen gas physisorption. The ideal conditions for the uptake of crystal violet dye were determined in batch experiments covering the standard parameters: pH, concentration, contact time, and adsorbent dosage. Experimental data are validated by applying Langmuir, Freundlich, Dubinin–Radushkevich, and Temkin isotherms. The thermodynamic parameters, ΔH°, ΔG°, and ΔS°, are calculated and it has been found that the adsorption process is spontaneous and endothermic with increasing disorder. An in-depth analysis of the kinetics of the adsorption process, order of the reaction and corresponding values of the rate constants was performed. The adsorption of crystal violet over OMC has been found to follow pseudo-second-order kinetics through a film diffusion process at all temperatures studied. Continuous flow column operations were performed using fixed bed adsorption. Parameters including percentage saturation of the OMC bed are evaluated. The exhausted column was regenerated through a desorption process and column efficiency was determined. Full article

Iodosilarene derivatives (PhIO, PhI(OAc)₂) constitute an important class of oxygen atom transfer reagents in organic synthesis and are often used together with iron-based catalysts. Since the factors controlling the ability of iron centers to catalyze alkane hydroxylation are not yet fully understood, the aim of this report is to develop bioinspired non-heme iron catalysts in combination with PhI(OAc)₂, which are suitable for performing C-H activation. Overall, this study provides insight into the iron-based ([Fe^II(PBI)₃(CF₃SO₃)₂] (1), where PBI = 2-(2-pyridyl)benzimidazole) catalytic and stoichiometric hydroxylation of triphenylmethane using PhI(OAc)₂, highlighting the importance of reaction conditions including the effect of the co-ligands (para-substituted pyridines) and oxidants (para-substituted iodosylbenzene diacetates) on product yields and reaction kinetics. A number of mechanistic studies have been carried out on the mechanism of triphenylmethane hydroxylation, including C-H activation, supporting the reactive intermediate, and investigating the effects of equatorial co-ligands and coordinated oxidants. Strong evidence for the electrophilic nature of the reaction was observed based on competitive experiments, which included a Hammett correlation between the relative reaction rate (logk_rel) and the σ_p (4R-Py and 4R’-PhI(OAc)₂) parameters in both stoichiometric (ρ = +0.87 and +0.92) and catalytic (ρ = +0.97 and +0.77) reactions. The presence of [(PBI)₂(4R-Py)Fe^IIIOIPh-4R’]³⁺ intermediates, as well as the effect of co-ligands and coordinated oxidants, was supported by their spectral (UV–visible) and redox properties. It has been proven that the electrophilic nature of iron(III)-iodozilarene complexes is crucial in the oxidation reaction of triphenylmethane. The hydroxylation rates showed a linear correlation with the Fe^III/Fe^II redox potentials (in the range of −350 mV and −524 mV), which suggests that the Lewis acidity and redox properties of the metal centers greatly influence the reactivity of the reactive intermediates. Full article

Crystal violet (CV) is an organic chloride salt and a triphenylmethane dye commonly used in the textile processing industry, also being used as a disinfectant and a biomedical stain. Although CV is widely used, it is carcinogenic to humans and is retained by industrial-produced effluent for an extended period. The different types of metal oxide (MO_x) have impressive photocatalytic properties, allowing them to be utilized for pollutant degradation. The role of the photocatalyst is to facilitate oxidation and reduction processes by trapping light energy. In this study, we investigated different types of metal oxides, such as titanium dioxide (TiO₂), zinc oxide (ZnO), zirconium dioxide (ZrO₂), iron (III) oxide (Fe₂O₃), copper (II) oxide (CuO), copper (I) oxide (Cu₂O), and niobium pentoxide (Nb₂O₅) for the CV decomposition reaction at ambient conditions. For characterization, BET and Raman spectroscopy were applied, providing findings showing that the surface area of the anatase TiO₂ and ZnO were 5 m²/g and 12.1 m²/g, respectively. The activity tests over TiO₂ and ZnO catalysts revealed that up to ~98% of the dye could be decomposed under UV irradiation in <2 h. The decomposition of CV is directly influenced by various factors, such as the types of MO_x, the band gap–water splitting relationship, and the recombination rate of electron holes. Full article

Synthetic dyes, exceeding 100,000 types on the market and produced at a global scale of over 700,000 tons annually, are extensively used in the textile industry. This industry, a leading contributor to water contamination, relies on dyes like reactive, azo, anthraquinone, and triphenylmethane, resulting in substantial water usage and significant effluent generation. A significant modern challenge is the pollution caused by dye-mixed wastewater, releasing hazardous chemicals into water bodies and posing threats to ecosystems, plants, and human health. Traditionally, physicochemical techniques have addressed textile dye-containing wastewater, but their drawbacks, including cost, inefficiency, and potential secondary pollution, have steered attention towards biological alternatives. Utilizing microorganisms and enzymes, these biological methods, such as microbial cell enzyme immobilization, the biofilm technique, bioreactors, biofuel/bioelectricity production, and genetic engineering, have emerged as promising, cost-effective, and environmentally friendly solutions for efficient dye removal from wastewater. This review paper specifically highlights advanced biological techniques and emphasizes their efficacy in addressing the challenges posed by synthetic textile dyes. Through a systematic review of recent research papers, published results, and observations, this review paper provides insights into emerging biological treatment strategies for effectively removing synthetic textile dyes and contaminants from wastewater. Full article

Dyes provide a notable environmental issue as a result of their intrinsic poisonous and carcinogenic characteristics. An estimated 60,000 metric tons of dyes has been discharged into the environment, leading to a substantial increase in water pollution. The mitigation of these dyes is a substantial and intricate challenge. The primary objective of this research is to conduct a comprehensive analysis of the adsorption of cationic dyes containing positively charged groups such as sulphonates, amines, and triphenylmethanes. The adsorption study was carried out using four different low-cost adsorbents derived from biowaste, specifically Groundnut Shell (GS), Mosambi Peel (MP), Mango Bark (MBARK), and Mango Leaves (ML). The adsorbent materials were characterized using FTIR, UV–Vis spectroscopy, scanning electron microscopy (SEM), point-of-zero charge (PZC), and BET techniques. The adsorption capacity was found to be between 1.5 and 2.2 mg/gm for Groundnut Shell, Mosambi Peel, Mango Bark, and Mango Leaves for individual dye removal (Crystal violet, Methylene blue, Rhodamine B, and Malachite green). It was observed that adsorbent derived from mango bark showed excellent adsorption (%) in a mono-component dye system and, thus, was explored for the simultaneous removal of a mixture of the same dyes. MBARK exhibited an excellent overall dye removal efficiency of 94.44% (Q_e = 2.7 mg/g) for the dye mixture in 60 min. From a detailed kinetic investigation, it was concluded that the adsorption followed the pseudo-second-order model (R²= 0.99963 to 1 for different dyes and adsorbents) hinting at chemisorption. The effect of the pH of the analyte solution and the dosage of adsorbent was also studied for simultaneous removal. The isothermal studies demonstrated that the Langmuir adsorption model (R² = 0.99416) was the best-fitted model, suggesting monolayer adsorption. The adsorption process was predicted to be governed by ion exchange, electrostatic interaction, hydrogen bonding, pi–pi interaction, etc., based on charge, functional groups, and pH of dyes and adsorbent. Thus, this study highlights the application of low-cost biowaste as a potential adsorbent for the mitigation of toxic industrial dyes present in wastewater. 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

To fully harness the potential of laccase in the efficient decolorization and detoxification of single and mixed dyes with diverse chemical structures, we carried out a systematic study on the decolorization and detoxification of single and mixed dyes using a crude laccase preparation obtained from a white-rot fungus strain, Pleurotus eryngii. The crude laccase preparation showed efficient decolorization of azo, anthraquinone, triphenylmethane, and indigo dyes, and the reaction rate constants followed the order Remazol Brilliant Blue R > Bromophenol blue > Indigo carmine > New Coccine > Reactive Blue 4 > Reactive Black 5 > Acid Orange 7 > Methyl green. This laccase preparation exhibited notable tolerance to SO₄²⁻ salts such as MnSO₄, MgSO₄, ZnSO₄, Na₂SO₄, K₂SO₄, and CdSO₄ during the decolorization of various types of dyes, but was significantly inhibited by Cl⁻ salts. Additionally, this laccase preparation demonstrated strong tolerance to some organic solvents such as glycerol, ethylene glycol, propanediol, and butanediol. The crude laccase preparation demonstrated the efficient decolorization of dye mixtures, including azo + azo, azo + anthraquinone, azo + triphenylmethane, anthraquinone + indigo, anthraquinone + triphenylmethane, and indigo + triphenylmethane dyes. The decolorization kinetics of mixed dyes provided preliminary insight into the interactions between dyes in the decolorization process of mixed dyes, and the underlying reasons and mechanisms were discussed. Importantly, the crude laccase from Pleurotus eryngii showed efficient repeated-batch decolorization of single-, two-, and four-dye mixtures. This crude laccase demonstrated high stability and reusability in repeated-batch decolorization. Furthermore, this crude laccase was efficient in the detoxification of different types of single dyes and mixed dyes containing different types of dyes, and the phytotoxicity of decolorized dyes (single and mixed dyes) was significantly reduced. The crude laccase efficiently eliminated phytotoxicity associated with single and mixed dyes. Consequently, the crude laccase from Pleurotus eryngii offers significant potential for practical applications in the efficient decolorization and management of single and mixed dye pollutants with different chemical structures. Full article

Microbial biotechnology plays a crucial role in improving industrial processes, particularly in the production of compounds with diverse applications. In this study, we used bioinformatic approaches to analyze the genomic architecture of Streptomyces albidoflavus MGMM6 and identify genes involved in various metabolic pathways that have significant biotechnological potential. Genome mining revealed that MGMM6 consists of a linear chromosome of 6,932,303 bp, with a high G+C content of 73.5%, lacking any plasmid contigs. Among the annotated genes, several are predicted to encode enzymes such as dye peroxidase, aromatic ring-opening dioxygenase, multicopper oxidase, cytochrome P450 monooxygenase, and aromatic ring hydroxylating dioxygenases which are responsible for the biodegradation of numerous endogenous and xenobiotic pollutants. In addition, we identified genes associated with heavy metal resistance, such as arsenic, cadmium, mercury, chromium, tellurium, antimony, and bismuth, suggesting the potential of MGMM6 for environmental remediation purposes. The analysis of secondary metabolites revealed the presence of multiple biosynthesis gene clusters responsible for producing compounds with potent antimicrobial and metal-chelating activities. Furthermore, laboratory tests conducted under controlled conditions demonstrated the effectiveness of MGMM6 in inhibiting phytopathogenic microbes, decolorizing and degrading aromatic triphenylmethane dyes, particularly Blue Brilliant G250, from wastewater by up to 98 ± 0.15%. Overall, the results of our study highlight the promising biotechnological potential of S. albidoflavus MGMM6. Full article

Phenolic antioxidants of various groups are important nutrients in the human diet, providing positive health effects. Nevertheless, these effects are dose dependent and require the control of natural phenolic contents in their sources. Coffee and citrus juices containing significant amounts of hydroxycinnamic acids and flavanones, respectively, are among the most widely consumed beverages all over the world. The electroactivity of phenolics allows the application of voltammetric sensors for quantification purposes. Highly sensitive and selective voltammetric sensors for the simultaneous quantification of hydroxycinnamic (caffeic (CA), ferulic (FA), and p-coumaric(p-CA)) acids and flavanones (hesperidin and naringin) have been developed for the first time using glassy carbon electrodes modified with single-walled carbon nanotubes functionalized via polyaminobenzene sulfonic acid (f-SWCNTs) and polymeric coverages from triphenylmethane dyes (phenol red (PR) or aluminon). Polymeric layers have been obtained in potentiodynamic modes. The conditions of the dye’s electropolymerization have been optimized using the voltammetric response of hydroxycinnamic acids or flavanone mixtures. Three separated oxidation peaks of CA, FA, and p-CA at the electrode with polyPR as well as hesperidin and naringin at the polyaluaminon-modified electrode have been observed. The oxidation currents are significantly increased comparing those at the bare glassy carbon (GCE) and carbon nanotube-modified electrodes. Both sensors provide a highly sensitive response to target analytes in the differential pulse voltammetric mode. Other natural phenolics of various classes do not affect the response of the sensors developed to the target analyte. The quantification of hydroxycinnamic acids in coffee and flavanones in orange and grapefruit juices has been successfully realized. Full article