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Extensive research in the last few decades has conclusively demonstrated the significant influence of experimental conditions, surfactants, and synthesis methods on semiconductors' properties in technological applications. Therefore, in this study, the synthesis of molybdenum oxide (MoO 3 ) was reported by the addition of 2.5 (MoO 3 _2.5), 5 (MoO 3 _5), 7.5 (MoO 3 _7.5), and 10 mL (MoO 3 _10) of nitric acid, obtaining the respective concentrations of 0.6, 1.10, 1.6, and 0.6 mol L -1 . In this study, all samples were synthesized by the hydrothermal method at 160 °C for 6 h. The materials obtained were structurally characterized by X-ray diffraction (XRD) and structural Rietveld refinement, Raman spectroscopy, and infrared spectroscopy (FTIR), confirming the presence of all crystallographic planes and bands associated with active modes for the pure hexagonal phase ( h -MoO 3 ) when the solution's concentration was 0.6 mol L -1 of nitric acid. For concentrations of 1.10, 1.60, and 2.10 mol L -1 , the presence of crystallographic planes and active modes associated with the formation of mixtures of molybdenum oxide polymorphs was confirmed, in this case, the orthorhombic, monoclinic, and hexagonal phases. X-ray photoelectron spectroscopy reveals the occurrence of the states Mo 4+ , Mo 5+ , and Mo 6+ , which confirm the predominance of the acid Lewis sites, corroborating the analysis by adsorption of pyridine followed by characterization by infrared spectroscopy. The images collected by scanning electron microscopy confirmed the information presented in the structural characterization, where microcrystals with hexagonal morphology were obtained for the MoO 3 _2.5 sample. In contrast, the MoO 3 _5, MoO 3 _7.5, and MoO 3 _10 samples exhibited hexagonal and rod-shaped microcrystals, where the latter morphology is characteristic of the orthorhombic phase. The catalytic tests carried out in the conversion of oleic acid into methyl oleate, using the synthesized samples as a heterogeneous catalyst, resulted in conversion percentages of 52.5, 58.6, 69.1, and 97.2% applying the samples MoO 3 _2.5, MoO 3 _5, MoO 3 _7.5, and MoO 3 _10, respectively. The optimization of the catalytic tests with the MoO 3 _10 sample revealed that the conversion of oleic acid into methyl oleate is a thermodynamically favorable process, with a variation in the Gibbs free energy between -67.3 kJ mol -1 and 83.4 kJ mol -1 as also, the energy value of activation of 24.6 kJ mol -1 , for the temperature range from 80 to 140 °C, that is, from 353.15 to 413.15 K, respectively. Meanwhile, the catalyst reuse tests resulted in percentages greater than 85%, even after the ninth catalytic cycle. Therefore, the expressive catalytic performance of the mixture of h -MoO 3 and α-MoO 3 (MoO 3 _10) phases is confirmed, associated with the synergistic effect, mainly due to the increase in the surface area and available Lewis sites of these phases.

The combination of materials to improve properties of interest has become one of the strategies widely used for numerous applications, including new catalysts, over the last few decades. In this study, silver molybdate (β-Ag 2 MoO 4 ) microcrystals were efficiently obtained by the hydrothermal method, obtaining composites with different amounts of graphene oxide (GO) (1, 2.5, 5, 7.5, and 10%, w/w) using the conventional hydrothermal method. The incorporation of GO on silver molybdate was confirmed by X-ray diffraction (XRD) and Raman spectroscopy, where the vibrational modes and crystallographic planes characteristic of the materials of interest were highlighted. The images collected by scanning electron microscopy (SEM) revealed the occurrence of plate-shaped structures (shells) anchored to the surface of the silver molybdate microcrystals (core). The optical properties showed that the materials presented E gap between 3.34 and 3.39 eV, where the sample with 7.5% of GO (GO@β-AgMo_7.5) was the one that presented energy for the conduction band, largely favorable to the formation of superoxide radicals through the photoexcitation process of electrons. The catalytic tests demonstrated that, among the samples obtained in this study, the sample with 7.5% of GO (GO@β-AgMo_7.5) exhibits superior photocatalytic performance against the dye rhodamine B (RhB) in an aqueous medium. Thus, the kinetics constant for photolysis (absence of catalysts) and for the sample β-AgMo and the sample with 7.5% of GO (GO@β-AgMo_7.5) are 0.38 × 10 -3 , 12 × 10 -3 , and 23.72 × 10 -3 min -1 , respectively. Therefore, it is 62.5 times more efficient in the degradation of the RhB dye, which confirms the promising photocatalytic properties of the obtained composite., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

Pseudomonas aeruginosa is a non-lactose fermenting Gram-negative bacteria responsible for causing numerous nosocomial infections. The present research aimed to analyze the anti-Pseudomonas aeruginosa potential of 2-Chloro-N-(4-fluoro-3-nitrophenyl)acetamide (A8). The antibacterial potential of A8 was evaluated from the Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC) and Association using the checkerboard method. MIC and MBC values were 512 µg/mL for all P. aeruginosa strains evaluated, demonstrating predominantly bactericidal activity. Furthermore, when A8 was associated with the drug ceftriaxone, pharmacological additivity and indifference were evidenced. In this sense, the synthetic amide was interesting, since it demonstrates the potential to become a possible candidate for an antimicrobial drug.

The Caatinga is an exclusively Brazilian biome where semiarid climatic conditions promote singularities in adaptive biodiversity. Many aromatic species are found in this region possessing antifungal properties, which are attributed to their essential oils. Thus, we questioned whether essential plant oils found in the Caatinga present anti-dermatophytic potential. Dermatophytes are keratinophilic fungi that cause one of the most prevalent mycoses globally, skin infections known as dermatophytoses (tineas). Here, we provide a comprehensive report of the available published information, analyzing the methods used to evaluate the antifungal activity, verifying the quality of the evidence and possible clinical applications, and discussing research trends in this area. The plants studied concentrated in the genera Croton (Euphorbiaceae), Lippia (Verbenaceae), Piper (Piperaceae), and Mentha (Lamiaceae). All of the studies used in vitro tests to analyze antifungal potential, and little evidence was ascertained concerning the mechanism of antifungal action. In addition, the essential oils also evidenced drug modifying activity of conventional antifungal drugs (Ketoconazole and Terbinafine). We believe that the anti-dermatophyte potential of plant essential oils occurring within the Caatinga is underestimated and that this review will encourage future chemical-pharmacological investigations into the plants within this biome.Key points• The essential oils from plants occurring in the Caatinga Biome present unknown anti-dermatophyte potential.• The studies against dermatophyte fungi concentrate on the families Lamiaceae and Verbenaceae.• In vitro assays were used to assess the anti-dermatophyte potential of the essential oils., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The continued contamination of water sources by pesticides is a problem that involves the life of aquatic organisms and human health, especially in countries whose economy is based on agriculture. The need to know the quality of drinking water under these circumstances is a priority for the public health of any community. Passive sampling methods allow the determination of long-term environmental pollutants through a single sample collection, reducing time and cost of analyses. One advantage of passive sampling is that it is possible to calculate a time-weighted average (TWA) concentration value or an equilibrium concentration value, depending on the type of device used and the exposure time. Passive sampling techniques using carbon nanomaterials (CNMs) have a high potential for pesticide sampling in aquatic systems. A device for passive sampling manufactured with CNMs in a microextraction system and recyclable materials was calibrated in laboratory exposure conditions over 15 days. The calibration results showed linear accumulation periods between 5 and 10 days. Sampling rates were between 0.014 and 0.146 mL day -1 . The sampler was field-tested in the San Francisco river basin in the state of Minas Gerais in Brazil for 7 days. This research allowed for the detection and calculation of TWA concentrations for organochlorine pesticides such as α-HCH, 4,4-DDE, and 4,4-DD in water sources. The manufactured device demonstrated greater sensitivity than the grab sampling processes for the detection of pesticides. The performed passive sampling system using gas chromatography/mass spectrometry (GC/MS) technique allowed for the collection, detection, identification, and quantification of 26 pesticides.

Herein, the structural defects of metal-free polymeric carbon nitrides were controlled by making use of different precursors in their syntheses, i.e. melamine (CN-M) and thiourea (CN-T), as well as a 1:1 mixture of them (CN-1M:1 T). By controlling the structural defects, the electronic, morphological and chemical properties were modified. Additionally, the activities of synthesized PCNs were evaluated for amoxicillin photodegradation under visible light irradiation (16 mW cm -2 ). The results of photocatalytic tests showed that CN-T material has better efficiency (100 % removal within 48 h), which is directly related to the greater number of defects present in its structure with consequent improvement of electron-hole pairs separation efficiency. The CN-T material showed excellent stability with only 13 % decrease in its photocatalytic activity after the third cycle. A mechanism for amoxicillin degradation by CN-T was proposed based on the ESI-MS and the in situ EPR allied with spin trapping method investigations., (Copyright © 2020 Elsevier B.V. All rights reserved.)

In this work, the potential to use an iron mining waste (IW), rich in α-Fe 2 O 3 and α-FeOOH, for the development of composites based on graphitic carbon nitride (CN) is demonstrated. These materials were synthesized through a simple thermal treatment at 550 °C of a mixture containing melamine and different IW mass percentages, giving rise to the catalysts xIWCN (where x is related to the initial mass percentage of IW). The iron phases of the precursor were partially transformed throughout the formation of the composites, in such a way that a mixture of α-Fe 2 O 3 and γ-Fe 2 O 3 was observed in their final composition. Furthermore, structural defects were produced in the carbonaceous matrix of the materials, causing the fragmentation of g-C 3 N 4 and an increase of surface area. The catalytic activities of these composites were evaluated in reactions of peroxymonosulfate activation for the degradation of paracetamol. Among these materials, the composite 20IWCN showed the best catalytic activity, being able to degrade almost 90 % of the total paracetamol in only 20 min of reaction. This catalyst also demonstrated high chemical stability, being successfully utilized in five consecutive reaction cycles, with negligible iron leaching., (Copyright © 2020 Elsevier B.V. All rights reserved.)

This research describes a solid-phase microextraction device using carbon nanomaterials supported on steel threads. The device was used to pre-concentrate and extract 24 pesticides in water. The carbon nanomaterials were obtained by a chemical vapor deposition (CVD) process, using methane and acetonitrile as carbon source. The different pesticides were separated, detected, and quantified using gas chromatography coupled to mass spectrometry (GC-MS). The system, optimized and validated in the laboratory, presented good results. Linearity was between 0.0007 and 50.00 μg L -1 , with determination coefficients greater than 0.9. The detection and quantification limits were in the range of 0.0002-1.1309 μg L -1 and 0.0007-3.7320 μg L -1 , respectively. The studied pesticides presented recovery values in the range of 70 ± 8 to 123 ± 18%. Carbon nanomaterials exhibited high thermal and mechanical resistance, as the same fiber could be used for approximately 300 extractions. The device was applied to analyze environmental water samples collected from the São Francisco river basin in Brazil and in the Chinampas in Mexico City., (Copyright © 2020 Elsevier B.V. All rights reserved.)

In this work, samples of Fe mining tailings from the collapsed Fundão Dam, Brazil, which were retained by the Candonga hydroelectric power plant, were characterized by various techniques. Quartz, hematite, kaolinite, and goethite were identified as the main phases present. The composition, homogeneity, and relatively low (~1%) organic matter content indicate potential for usage of these tailings in civil constructions. The next step of this work is to investigate such applications. If their feasibility is confirmed, the goal is to use this material for construction in the areas affected by the Fundão Dam rupture. This use will lead to positive socio-environmental impacts in these regions, where tailings still need to be removed and damaged infrastructure needs to be repaired. Integr Environ Assess Manag 2020;16:636-642. © 2019 SETAC., (© 2019 SETAC.)

Cryptococcus neoformans is a yeast fungus, which causes cryptococcosis, triggered by basidiospore inhalation and consequent dissemination to the central nervous system. In this study, we analyzed the antifungal action of thymol against 10 clinical strains of C. neoformans and analyzed the interaction of this monoterpene with sterols. The MICs of thymol ranged from 20 to 51 μg/ml, while the MFC values varied between 40 and 101 μg/ml. For the strains ICB-2601 and LM-39, in the presence of ergosterol, the MIC of thymol was 64 μg/ml, and in the presence of cholesterol, its MIC was 32 μg/ml. Based on the results, thymol presents antifungal action and seems to interact with ergosterol, but not with cholesterol. Complementary studies are needed to analyze its full effects.

This work reports the use of an iron ore tailings from waste dam as a catalyst and support for carbon nanotubes synthesis and their application in the adsorption of the 17α-ethinylestradiol hormone. The synthesis was carried out by Chemical Vapor Deposition (CVD) in a Fluidized Bed system using: ethylene at temperatures of 500, 600 and 700 °C, and acetonitrile at 500, 600, 700, 800 and 900 °C. The transmission electron microscopy (TEM) results showed that the two higher temperatures in each case favored the formation of nanostructures like carbon nanotubes (CNTs), with good yields. The ethylene source generated classic tubular structures of multiple walls. On the other hand, acetonitrile provided the formation of tubes with less organization, known as bamboo like. This morphology was caused by the insertion of nitrogen into the graphite structure (doping), which originates from the carbon source. The adsorptive capacity of the materials for 17α-Ethinylestradiol removal ranging from 9.2 mg g -1 to 22.3 mg g -1 . The kinetic and adsorption isotherm studies were also performed for the systems. As for kinetics, all of them presented pseudo-second order behavior. In relation to the type of isotherm, the systems showed Freundlich behavior, that is, the adsorption occurs in multiple layers. Finally, it was concluded that the use of an iron ore tail as a catalyst in the production of CNTs by CVD is feasible. The materials synthesized still had good adsorptive capacity for an emerging contaminant, thus this study allowed the investigation of two environmental problems., Competing Interests: Declaration of competing interest None., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In this work, magnetic cobalt nanoparticles (CoNPs) were synthesized and applied to the removal of Remazol golden yellow RNL (RGY) from aqueous solutions and textile wastewater. The CoNPs were characterized and the Co content found in the CoNPs was 60.38% (m/m). The analysis of X-ray Diffraction (XRD) and Raman Spectroscopy indicated the presence of Co 0 and CoO in the composition of the material, as confirmed by Thermogravimetric Analysis coupled to Mass Spectrometry (TG-MS). Images obtained by the Transmission Electron Microscope (TEM) showed that the CoNPs have sizes smaller than 10 nm, sphere morphology and high agglomeration capacity. The results obtained by nitrogen adsorption-desorption suggested that the nanomaterial presented a mesoporous characteristic, low specific surface area (15.70 m 2  g -1 ) and a pore volume and pore diameter of 0.072 cm 3  g -1 and 3.64 nm, respectively. CoNPs removed the RGY with high efficiency, reaching almost 100% removal in 30 min. The kinetic results showed that the reaction followed pseudo-second-order kinetics. Additionally, the removal process can be altered depending on the experimental condition. For instance, under acidic conditions, the reductive degradation prevailed, while in neutral or basic conditions, two simultaneous processes occur: reductive degradation and adsorption. Finally, CoNPs were applied to textile wastewater. The results showed high discoloration, reaching almost 88%. However, there was only a 32% decrease in chemical oxygen demand, showing that CoNPs are efficient at removing organic dyes from aqueous solutions., (Copyright © 2019. Published by Elsevier Ltd.)

Amphiphilic magnetic composites were produced based on chrysotile mineral and carbon structures by chemical vapor deposition at different temperatures (600-900 °C) and cobalt as catalyst. The materials were characterized by elemental analysis, X-ray diffraction, vibrating sample magnetometry, adsorption and desorption of N2, Raman spectroscopy, scanning electronic microscopy, and thermal analysis showed an effective growth of carbon structures in all temperatures. It was observed that at 800 and 900 °C, a large amount of carbon structures are formed with fewer defects than at 600 and 700 °C, what contributes to their stability. In addition, the materials present magnetic phases that are important for their application as catalysts and adsorbents. The materials have shown to be very active to remove the oil dispersed in a real sample of emulsified wastewater from biodiesel production and to remove methylene blue by adsorption and oxidation via heterogeneous Fenton mechanism., (Copyright © 2016 Elsevier Ltd. All rights reserved.)