Search

The crystal violet (CV) staining technique represents a prevalent approach for the development of latent fingerprints, especially on adhesive tape surfaces. Nevertheless, the technique necessitates intricate formulations to augment its performance. In this investigation, an optimized CV staining protocol was developed, characterized by the absence of residual dye on the target substrates and the capability of facilitating fingerprint visualization under ambient light conditions. Four donors, comprising two males and two females, deposited natural fingerprints on various substrates, including glass microscope slides, aluminum foil, and 115 g glossy coated paper, without any specific guidelines. Fingerprints developed using cyanoacrylate fuming served as benchmarks and were contrasted with those generated through alternative methods: CV, ardrox, rhodamine 6G, powdering, and the optimized CV staining protocol. The fingerprint development experiment was replicated at seven distinct time intervals, encompassing 1 day, 1 week, 1, 3, 6, 9, and 12 months, resulting in a dataset of 420 fingerprints. The evaluation of fingerprint identifiability employed a scoring system established by the Home Office Centre for Applied Science and Technology. The results indicated that the optimized CV staining technique demonstrated superior performance, boasting a 92.9% rate of identifiable fingerprint development in contrast to other employed methodologies. Consequently, this optimized CV staining approach is recommended as an efficient, rapid, and straightforward critical dyeing method, applicable to a wide array of substrates in forensic investigations., (© 2024 The Authors. Journal of Forensic Sciences published by Wiley Periodicals LLC on behalf of American Academy of Forensic Sciences.)

Presence of copying pencils in heritage objects poses a significant challenge for conservators due to their proneness to fading, sensitivity to solvents and difficulties in differentiation from regular graphite pencils. In this paper a method of copying pencils identification by means of ATR—FTIR spectroscopy is used. A protocol for spectra processing and dimensionality reduction of spectral data by means of principal component analysis has been developed, allowing for pencil types differentiation and providing an easy to read visual representation of the collected data. The protocol has been developed on mock-up samples and tested on objects from the archives of the State Museum Auschwitz – Birkenau. [ABSTRACT FROM AUTHOR]

Facile fabrication of flexible substrates containing high concentration of nanoparticles (NPs) is very promising owing to their capability of swab-based surface-enhanced Raman scattering (SERS) trace detection. However, the background signal of the substrate could compromise the trace-detection capabilities. Moreover, the presence of fluorescent molecules may result in intense fluorescence background which could overshadow the Raman peaks. Herein, we demonstrate that the surfactant-free bimetallic (Ag and Au) NPs, synthesized directly on the filter paper, are very effective in reducing the background signal in SERS-based trace detection. Simple soaking of filter paper in a mixture of HAuCl 4 and AgNO 3 solution, and its immediate drying and reduction produces Au-Ag alloy NPs on the filter paper. Interestingly, the substrates are very effective in quenching the background fluorescence of both filter paper and the analyte, thereby effectively detecting the SERS signature of the fluorescent molecules. In particular, Rhodamine6G (R6G) concentrations down to 10−10 M were detected under resonance excitation, both by solution drying and swabbing. The swab detection of ammonium nitrate, which is usually used in homemade explosives, was also demonstrated. Moreover, owing to the fluorescence quenching properties, the Au-Ag alloy substrates (AuAgS) were able to carry out the swab-based multiplex-detection of crystal violet (CV), Brilliant Cresyl Blue (BCB), and R6G upon resonance excitation of R6G. Finally, the substrates have shown good reproducibility, stability, and signal uniformity. This verifies the potential of AuAgS for real-world trace-detection applications. [ABSTRACT FROM AUTHOR]

One of the methods to solve the problem of lead metal in water is adsorption. One of the adsorbents that can be used is cellulose because it has an active group that can bind Pb(II). In this study, cellulose from the HVS wastepaper was used as the adsorbent to adsorb the Pb metal. HVS wastepaper was extracted with 10% w/v NaHCO3 and refluxed with 5% w/v Na2HPO4. Cellulose was characterized using Fourier Transforms Infrared Spectroscopy (FTIR) and Scanning Electron Microscope (SEM). Pb(II) adsorption was carried out by the batch method, and it was evaluated using Atomic Absorption Spectrophotometry (AAS) with varying adsorbent mass, concentration, contact time, and pH. FTIR characterization showed that the presence of O - H, C - H, C = O, and C - O groups played a role in the adsorption process. The surface morphology of cellulose from SEM analysis showed form like a fiber shape with agglomerated fine particles. The optimum conditions for adsorption were 0.100 g of adsorbent mass, Pb(II) concentration of 105 ppm, contact time of 10 minutes, and pH of solution 5. An adsorption isotherm model that is preferable for this adsorption process is the Freundlich isotherm model. From the results of this study, HVS paper waste can be used as an adsorbent to handle Pb(II) metal ions to be an alternative as a lowcost adsorbent. [ABSTRACT FROM AUTHOR]

We present a tilted fiber Bragg grating (TFBG) sensor coated with crystal violet/perfluorinated sulfonic acid (CV/Nafion) composite film for relative humidity (RH) monitoring. The composite film demonstrates the characteristics of an optical "humidity test paper" by exhibiting a color transition from yellow to green within a RH range of 10 % to 80 %. This color variation indicates its potential to effectively monitor RH levels in diverse environments. To achieve a quantitative RH sensing, we coat CV/Nafion composite film on an etched TFBG (ETFBG), where surrounding RH changes can be measured from spectral responses of ETFBG transmission. In experiments, the proposed the CV/Nafion-coated ETFBG sensor exhibits RH sensitivities of 0.068 dB/%RH and 3 pm/%RH for intensity change and wavelength shift measurements, respectively, within a relative humidity (RH) range of 10 % to 80 %. Additionally, based on intensity measurement, short response and recovery times of ∼4.4 and ∼4.6 s are estimated from a continuous RH monitoring. • The proposed sensor's color will change from yellow to green with the increasing of the RH. • The proposed sensor could be used for RH detection of liquids, gases, and solids. • High RH detection sensitivity of 0.068 dB/% RH was obtained. • The response and recovery times are 4.4 s and 4.6 s respectively. [ABSTRACT FROM AUTHOR]

Gamma radiations are known to bring about radiolysis of myriad compounds / dyes which is used to measure of the energy of the incident radiation on the system. The use of various dye solutions for chemical dosimetry is reported in literature. Various thin film dosimeters, semi-conductor dosimeters are also reported and widely used. Similarly ? - dose quantification using paper or polymer impregnated with dyes has also been reported. In the present study, decolouration due to gamma radiation of various dye impregnated papers viz. Gentian Violet (GV), Malachite Blue (MB), Malachite Green (MG), Brilliant Yellow (BY) and Congo Red (CR) has been investigated using device independent colour parameters. The colour analysis was done by standard procedures of Commission Internationale de l'Eclairage CIE. Color has mind dependency so to eliminate the errors in determination colour parameters are evaluated. [ABSTRACT FROM AUTHOR]

[Display omitted] • Inkjet printing Ag nanoparticles on paper coated with chitosan or N,N, N -trimethyl chitosan to obtain SERS substrates. • Biopolymer coatings not only reduce the rugosity and porosity of the paper but also confer hydrophobicity to the paper. • SERS sensitivity and reproducibility was improved when compared with non-coated counterparts. Paper-based sensors for surface-enhanced Raman scattering (SERS) detection of water pollutants have gained much attention in the last decades. However, most of the fabricated paper-based SERS substrates still face some limitations regarding reproducibility and uniformity. In this work, we report the fabrication of hydrophobic paper-based SERS substrates with high reproducibility and uniformity by inkjet printing Ag colloidal nanoparticles (NPs) on office paper pre-treated with chitosan (CH) or N,N, N -trimethyl chitosan (TMC). We demonstrate that the previous coating of paper with such biopolymers substantially improves the SERS performance of the paper substrates. In screening experiments, crystal violet (CV) 100 μM was used as molecular probe, leading to an increase of about 9- and 7-fold in the observed SERS intensity when the papers were coated with CH and TMC, respectively. Also, the reproducibility of the substrates coated with the biopolymers increased more than 2 times compared to non-coated office paper. We suggest that the improved performance of the coated substrates is related to a more uniform deposition of the AgNPs on the paper surface due to the hydrophobic nature, low porosity and roughness of the coated paper. [ABSTRACT FROM AUTHOR]

This study aimed to evaluate the activity, resistance, clonality of MIC distribution, and the correlation between virulence and resistance genes and biofilm formation of omadacycline (OMC) in clinics for Streptococcus agalactiae isolates from China. 162 isolates were collected retrospectively in China. The S. agalactiae were collected from the body's cervical secretions, wound secretions, ear swabs, secretions, semen, venous blood, cerebrospinal fluid, pee, etc. The MIC of OMC against S. agalactiae was determined by broth microdilution. The inhibition zone diameters of OMC and other common antibiotics were measured using filter paper. D-test was performed to determine the phenotype of cross resistance between erythromycin and clindamycin. In Multilocus sequence typing (MLST), some commonly-detected resistance genes and virulence gene of these S. agalactiae isolates were investigated using polymerase chain reaction (PCR). Biofilms were detected by crystal violet staining. Our data demonstrated the correalation of the biofilm formation and OMA antimicrobial susceptibility of S.agalactiae clinical isolates with the carrier of virulence gene scpB. Conclusively, OMC exhibits the robust antimcirobial activity against clinical S. agalactiae isolates from China compared with DOX or MIN, and the carrier of the virulence gene scpB might correlate with the biofilm formation in OMC-resistant S. agalactiae. [ABSTRACT FROM AUTHOR]

In this work, we have proposed a new approach to study the mechanism of crystal violet (CV) photodegradation on TiO 2 surface using kinetic Monte Carlo simulation. The TiO 2 surface was considered as a set of reactive centers, which is essential in dye photodegradation. A new variable "the effective photon concentration" (I eff ) is defined. A detailed chemical understanding of the photocatalytic reaction is provided. This approach provides a simple and effective method to find the optimal conditions of the studied system. This goal was achieved by investigating the effects of some operational parameters, including initial concentration of CV, pH, loading TiO 2 , light intensity and volume, on the degradation percent, and also, on the effective photon concentration. The perfect agreements between the experimental and simulated data at different conditions confirmed the proposed approach for describing the CV photodestruction. Also, the simulation results indicated that: (1) a significant fraction of the scattered UV irradiation into the reaction vessel does not lead to charge carrier generation; (2) the generation and recombination of charge carriers have crucial roles in the photodegradation. This is the first time that a method based on the reactive centers is employed to investigate the dye degradation by a photocatalyst., (© 2021 American Society for Photobiology.)

In this work, we demonstrate a seeded approach for in-situ growth of Ag nanostructures directly on filter paper. Multiple growth steps were used to increase the size of Ag NPs grown from Au seeds. Essentially, this procedure generated a high density of NPs on filter paper which in turn provided high enhancement of Raman signals. We have seen a marked increase in the SERS enhancement factor with each growth step. Moreover, the relative standard deviation (RSD) values decreased with each growth step, indicating the relatively uniform distribution of NPs on the substrate. With four growth steps, we were able to achieve an EF of 9.28 × 104 with RSD values of 14%. In particular, the detection limit of 10 nM for CV has been achieved by both solution drying and swabbing. Moreover, swab detection of explosive material ammonium nitrate down to 100 µM has also been demonstrated. [ABSTRACT FROM AUTHOR]

In this paper, a NiAl-LDH with the characteristic structure of a hydrotalc-like compound was applied as a carrier in a two-step hydrothermal process, and a MnCdS/In2S3/NiAl-LDH composite material was successfully prepared by loading MnCdS and In2S3 on the flower spherical-like surface of NiAl-LDH. The combination of NiAl-LDH with In2S3 and MnCdS made the band gap smaller and the light absorption range larger, thus increasing the utilization rate of light. 50% MnCdS/In2S3/NiAl-LDH composites had the best photoinduced charge separation and highest surface enrichment of photogenerated electrons. In the degradation experiment of crystal violet (CV), 50% MnCdS/In2S3/NiAl-LDH composites showed superior photocatalytic degradation efficiency (>98.5%) under full spectrum light. Furthermore, the applicability and universality of photocatalysts were studied by observing the degradation of CV by MnCdS/In2S3/NiAl-LDH composites under different conditions. In addition, the composites showed excellent hydrogen production capacity in the photolysis of water, in which hydrogen production within 8 hours was about 7661.51 μmol g−1. By combining the results of active species capture experiments, density functional theory (DFT) calculations and photoelectrochemical experiments, the possible mechanism of double S-scheme heterojunction photocatalysis among NiAl-LDH, In2S3 and MnCdS was inferred, which is one of the main reasons for the enhancement of photocatalytic activity. [ABSTRACT FROM AUTHOR]

In this research, aluminum metal-organic framework encapsulated with poly (itaconic acid) grafted crosslinked chitosan composite sponge (Al-MOF@PIC) was prepared. SEM, FTIR, XPS, XRD, and BET techniques were employed to thoroughly characterize the synthesized material and establish its structure and characteristics. The study discovered that the Al-MOF@PIC is an efficient way to remove dyes, which constitute a significant number of contaminants in industrial wastewater. Subsequently the adsorption of methyl violet 2B (MV-2B) dye, the surface area, pore size, and pore volume of the adsorbent decreased from 1860.68 m 2 /g, 1.62 nm, and 1.52 cc/g to 1426.45 m 2 /g, 1.11 nm, and 0.92 cc/g, individually. This modification suggested that a portion of the MV-2B dye had been removed by adsorption over the adsorbent's pores. The excellent adsorption capacity of the material was further confirmed by batch adsorption tests, which displayed a maximum adsorption capability of 646.76 mg/g for the elimination of MV-2B dye. The high adsorption energy of 26.8 kJ/mol designates that chemisorption is primarily responsible for MV-2B dye adsorption against the sponge adsorbent. The Al-MOF@PIC composite sponge demonstrated exceptional reusability over six cycles, demonstrating its strength and durability. The Al-MOF@PIC composite sponge successfully removes MV-2B from water by pore filling, π-π stacking, hydrogen bonding, and electrostatic interactions, which are the key mechanisms behind the adsorption of the dye pollutant. Its potential for practical applications is further demonstrated using Box Behnken-design (BBD) to optimize the adsorption consequences., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In today's world, major pollutants, such as cationic dyes and heavy metals, pose a serious threat to human health and the environment. In this study, a novel adsorbent was created through the electrospinning of polyvinyl alcohol/polyacrylic acid (PVA/PAA), incorporated with hexagonal boron nitride (hBN) coated with polydopamine (PDA). The integration of hBN and PDA substantially enhanced the adsorption capacity of the PVA/PAA fibers, making them highly effective in adsorbing cationic dyes such as methylene blue and crystal violet, as well as cobalt (II) ions, from contaminated water. The adsorbents were assessed to understand how their adsorption behavior varies with pH, as well as to examine their adsorption kinetics and isotherms. The results indicate that the PVA/PAA-hBN@PDA adsorbent has maximum adsorption capacities of 1029.57 mg/g, 793.65 mg/g, and 62.46 mg/g for methylene blue, crystal violet, and cobalt (II) ions, respectively. This underscores the superior performance of the PVA/PAA-hBN@PDA adsorbent when compared to both the PVA/PAA and PVA/PAA-hBN adsorbents. The adsorption kinetics adhered to a pseudo-second-order model, indicating chemisorption, whereas the Langmuir model implied a monolayer adsorption. Overall, the findings of this study highlight the efficacy of harnessing the synergistic capabilities of hBN and PDA within the PVA/PAA-hBN@PDA adsorbents, providing an efficient and eco-friendly approach to removing cationic dyes and heavy metals from contaminated water, and thereby contributing to a cleaner and safer environment for all., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Nahid Azizi, Shaghayegh Goudarzi, Reza Eslami reports financial support was provided by Mitacs Canada. Nahid Azizi, Reza Eslami reports financial support was provided by Sensofine Inc. Hadis Zarrin reports financial support was provided by Natural Sciences and Engineering Research Council of Canada. Nahid Azizi, Shaghayegh Goudarzi, Reza Eslami reports financial support was provided by Toronto Metropolitan University Faculty of Engineering & Architectural Science. Nahid Azizi, Shaghayegh Goudarzi, Reza Eslami reports financial support was provided by Toronto Metropolitan University. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Silver nanowire ink was written on the surface of drawing paper by automatic writing method. The prepared silver nanowires arrays showed good SERS activities, uniformity and repeatability. Furthermore, silver nanowires arrays were also relatively stable that SERS signals were still observed after ten weeks. [Display omitted] • Silver nanowires arrays were prepared by automatic writing method. • The detection limit of crystal violet adsorbed on the arrays was down to 10-15 mol/L. • The arrays exhibited good uniformity and repeatability with RSD of about 10%. • Crystal violet residue was successfully detected by continuously pressing nine times. • The quantitative analyses of 2, 2′-bipyridyl were achieved based on the arrays. Silver nanowire ink was written on the surface of drawing paper by automatic writing method. Scanning electron microscopy was used to characterize the surface morphologies of the drawing paper before and after writing silver nanowires. The effects of fabrication parameters and measurement parameters on silver nanowires arrays were investigated. Crystal violet was selected as the probe molecule to study the SERS performance of silver nanowires arrays. The detection limit of crystal violet was as low as 10-15 mol/L. The uniformity and repeatability of the arrays were also explored, and the relative standard deviation values were about 10%. Moreover, silver nanowires arrays were also relatively stable that SERS signals were still observed after ten weeks. Detection of the crystal violet residue was further achieved on the substrates by continuously pressing nine times. In addition, silver nanowires arrays were also applied to the quantitative analyses of 2, 2′-bipyridyl. [ABSTRACT FROM AUTHOR]

Insufficient dental restoration finishing and polishing may lead to plaque accumulation, gingival inflammation, staining, caries, and esthetic impairment. Here, the effect of two finishing and polishing systems on surface roughness and bacterial adhesion were evaluated. Two finishing and polishing kits were evaluated: diamond burs (Shine 1-2, Strauss & Co, Raanana, Israel) and paper discs (Sof-Lex 3M ESPE, Seefeld, Germany) (n = 30 each). For each group surface roughness was evaluated using an optical profilometer (Contour GT-K1, Bruker, Billerica, MA, USA) (n = 10). Surface bacteria were evaluated for biofilm biomass using crystal violet (CV) staining (absorbance measured at 538 nm) and viable counts (CFU/mL) (n = 20). The control group included polymerized discs against a Mylar strip (n = 30). Student's t test and one-way ANOVA were used for statistical evaluation. Diamond burs, paper discs, and control average surface RA were 169.4 ± 45.2 µ, 364 ± 77.7 µ, and 121.2 ± 18.1 µ, respectively. There was a significant difference found between all groups (p < 0.00001). Bacterial biomass on diamond burs, paper discs, and control samples were 0.458 ± 0.161, 0.507 ± 0.139, and 0.446 ± 0.142, respectively (p = 0.257). Viable bacterial counts (CFU/mL) on diamond burs, paper discs, and control samples were 2.25 × 104, 2.95 × 104, and 2.75 × 104, respectively (p = 0.856). A comparison between two finishing and polishing kits showed that the shine 1–2 diamond bur kit produced a smoother surface than the polishing disc kit. No differences were found in the biofilm biomass quantification and bacterial viable count between the groups. [ABSTRACT FROM AUTHOR]

Ionizing radiation (mainly including gamma ray and electron beam) technology provides a more efficient and ecological option for dye-containing wastewater treatment, which is supported by its successful achievements in industrial-scale applications. However, the degradation pathway of triphenylmethane dyes by radiation technology is still unclear. In this study, crystal violet (CV) was selected as representative cationic triphenylmethane dye, the decolorization and degradation performance by electron beam radiation technology was systematically evaluated. The results showed that CV can be efficiently decolorized and mineralized by radiation, and its degradation kinetics followed the first-order kinetic model. The effect of inorganic anions and chelating agents commonly existed in dye-containing wastewater on CV decolorization and total organic carbon (TOC) removal was explored. Quenching experiments, density functional theory (DFT) calculation and high performance liquid chromatography mass spectrometry (HPLC-MS) analysis were employed to reveal CV decolorization and degradation mechanism and pathway, which mainly included N-demethylation, triphenylmethane chromophore cleavage, ring-opening of aromatic products and further oxidation to carboxylic acid, and mineralization to CO 2 and H 2 O. Additionally, electron beam radiation/PMS process was explored to decrease the absorbed dose required for decolorization and degradation, and the synergetic effect of radiation with PMS was elucidated. More importantly, the findings of this study would provide the support for treating actual dyeing wastewater by electron beam radiation technology., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

In the study, a novel chitosan biopolymer and 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid (IL)-incorporated sulfonated poly (ether ether ketone) (SPEEK) composite (Ch-IL@SPEEK) was prepared for adsorption of cationic crystal violet (CV) dye. The proposed composite was well characterized by several techniques. CV adsorption performance was examined via batch studies by varying various variables involving adsorbent dosage, contact time pH and temperature. The isotherm results were demonstrated the adsorption characters of the processes were Langmuirian. The maximum adsorption capacity was determined as 77.66 mg g -1 for the composite which was significantly higher than SPEEK (q max  = 45.36 mg g -1 ). The determined equilibrium time of the operated system was 360 min and the kinetic model was assessed as Elovich. At low pHs the protonated surface groups repelled the positively charged CV and the adsorption rate increased with increasing pH. The process is spontaneous and favorable as it proceeds via endothermic interactions. Furthermore, even at the end of 5 successful adsorption cycles, 77.86 % CV removal was obtained. Remarkable efficiencies were also achieved in the removal performance of different organic pollutants. Based on the reported results, Ch-IL@SPEEK composite were exhibited as an impressive adsorbent material for adsorption processes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Purpose: To evaluate the value of calcofluor white in the diagnosis of invasive fungal disease (IFD)., Methods: A total of 84 patients with possible pulmonary fungal infection who underwent bronchoscopy with bronchoalveolar lavage fluid (BALF) were included. All BALF specimens were subjected to Calcofluor white (CFW), potassium hydroxide (KOH) and Gram stains., Results: CFW has the most sensitivity than KOH and Gram staining. The specificity of CFW was 92.00 %, which was lower than that of Gram staining. The PPVs for CFW, KOH and Gram staining were 94.44 %, 84.62 % and 80.00 % respectively. The NPVs for CFW, KOH and Gram staining was 47.92 %, 32.39 % and 30.38 % respectively. The AUCs of these three methods were 0.748, 0.550 and 0.510 respectively., Conclusion: CFW is superior to KOH and Gram staining in the diagnosis of invasive fungal diseases., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

This document is a correction notice for an article titled "The BRD4 inhibitor JQ1 augments the antitumor efficacy of abemaciclib in preclinical models of gastric carcinoma." The authors identified minor errors in the image-typesetting in Figure 3 of the original article. The image for the NCI-N87 cell line in Figure 3C was mistakenly included, and the corresponding statistical analysis for NCI-N87 in Figure 3D needs to be corrected. The corrected figure has been provided, and the correction does not affect the results or conclusions of the paper. The correction notice is authored by Mei Feng, Hao Xu, Wenyuan Zhou, and Yisheng Pan. [Extracted from the article]

In this study, a highly sensitive and quick electrochemical platform based on poly (crystal violet) film and copper oxide nanoparticles for the detection of brilliant blue FCF from various soft beverages was developed. The synthesized copper oxide nanoparticles were investigated with Fourier transform infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray. Further, crystal violet was electropolymerized on the surface of the carbon paste electrode modified with copper oxide nanoparticles. The electrochemical properties of poly (crystal) violet/copper oxide nanoparticles modified carbon paste electrode were assessed through the utilization of cyclic voltammetry and electrochemical impedance spectroscopy. Furthermore, the signal towards the oxidation of brilliant blue was examined using the differential pulse voltammetry method. Under ideal experimental conditions, the peak current exhibited a linear relationship with the brilliant blue concentration within the range of 0.01-1.00 nmol/L, with a sensitivity of 294.55 µA nmol/L cm -2 and a significant detection limit of 3 pmol/L. In the presence of other dyes and other food additives, the developed platform showed greater selectivity in detecting brilliant blue. The reliability of the designed platform was demonstrated by the 99.19 - 100.67 recovery percentage for the identification of BB in various soft drink samples., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Unchecked dye effluent discharge poses escalating environmental and economic concerns, especially in developing nations. While dyes are well-recognized water pollutants, the mechanisms of their environmental spread are least understood. Therefore, the present study examines the partitioning of Acid Orange 7 (AO7) and Crystal Violet (CV) dyes using water-sediment microcosms and reports that native microbes significantly affect AO7 decolorization and transfer. Both dyes transition from infused to pristine matrices, reaching equilibrium in a fortnight. While microbes influence CV partitioning, their role in decolorization is minimal, emphasizing their varied impact on the environmental fate of dyes. Metagenomic analyses reveal contrasting microbial composition between control and AO7-infused samples. Control water samples displayed a dominance of Proteobacteria (62%), Firmicutes (24%), and Bacteroidetes (9%). However, AO7 exposure led to Proteobacteria reducing to 57% and Bacteroidetes to 3%, with Firmicutes increasing to 34%. Sediment samples, primarily comprising Firmicutes (47%) and Proteobacteria (39%), shifted post-AO7 exposure: Proteobacteria increased to 53%, and Firmicutes dropped to 38%. At the genus level, water samples dominated by Niveispirillum (34%) declined after AO7 exposure, while Bacillus and Pseudomonas increased. Notably, Serratia and Sphingomonas, known for azo dye degradation, rose post-exposure, hinting at their role in AO7 decolorization. Conversely, sediment samples showed a decrease in the growth of Bacillus and an increase in that of Pseudomonas and Serratia. These findings emphasize the significant role of microbial communities in determining the environmental fate of dyes, providing insights on its environmental implications and management., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

In the former section of the present paper, the prospective application of B. mojavensis BI2 derived lipopeptides for dyes biodecolorization was demonstrated. The lipopeptide was mainly composed of linear and cyclic Fengycin and Surfactin isoforms. When using 100 mg/L, we are able to remove about 98% of 100 and 200 mg/L Malachite Green (MG). For the Crystal Violet (CV), the % of biodecolorization does not exceed 85% in the presence of 100 and 400 mg/L BI2 lipopeptide. In the second part of the paper, we proved the efficiency of dyes biosorption by palm waste floor, optimized by a Taguichi design. The bio-treatment efficiency was evaluated by color removal and the enhancement of germination index. Optimum treatments were obtained with 10 g/L and 6 g/L palm waste for 200 mg/L MG and CV respectively during 1 hour. Nevertheless, BI2 lipopeptide addition has no significant effect on color biosorption by date palm waste flour. [ABSTRACT FROM AUTHOR]

Industrial dyes are considered one of the main causes of increased water pollution of water. Many businesses, such as steel and paper, are located along riverbanks because they require large amounts of water in their manufacturing processes, and their wastes, which contain acids, alkalis, dyes, and other chemicals, are dumped and poured into rivers as effluents. For example, chemical enterprises producing aluminum emit a significant quantity of fluoride into the air and effluents into water bodies. Fertilizer facilities produce a lot of ammonia, whereas steel plants produce cyanide. Many nations consider employing wastewater treatment plants using physical, biological, and chemical methods to clean the wastewater to address environmental crises. The treated water can be used for targeting the irrigation systems in its majority, as it is biologically acceptable for that specific use, industrial dyes are considered one of the leading causes of increased water pollution of water. Many businesses, such as steel and paper, are located along riverbanks because they require large amounts of water in their manufacturing processes, and their wastes, which contain acids, alkalis, dyes, and other chemicals, are dumped and poured into rivers as effluents. For example, chemical enterprises producing aluminum emit a significant quantity of fluoride into the air and effluents into water bodies. Fertilizer facilities produce much ammonia, whereas steel plants produce cyanide. Chromium salts are used in. Many nations consider employing wastewater treatment plants using physical, biological, and chemical methods to clean the wastewater to address environmental crises. The treated water can target the majority of irrigation systems, as it is biologically acceptable for that specific use, which economizes the use of freshwater sources for municipal use. This study presents a novel method for fabricating an efficient adsorbent sheet for wastewater treatment. The sheets are fabricated by combining sugarcane bagasse pulp as a scaffold with commercial, naturally activated carbon, and bimetallic‐prepared adsorbents. Sugarcane bagasse is utilized in producing activated carbon because of its high carbon contents, availability, and low cost. The prepared composite sheets are synthesized and investigated for pollutants removal of crystal violet (CV), methyl orange (MO), and Chromium (CI) dyes. Different weight ratios of activated carbon are used to form a bio‐composite mixed sheet. The formed sheets' morphology is performed via a high scanning electron microscope (SEM) and Fourier Transform Infrared Spectroscopy (FTIR). To determine the adsorption mechanism, the intra‐particle diffuse screening experiment is used to test the experimental data. All the prepared sheets can retain the pollutants, with the best removal efficiency of 98% for methyl orange adsorption onto the bio‐composite mixed sheet. The results of the parameter (time, concentration, and dose) sets provided valuable proof that the adsorption of methyl orange onto the bio‐composite sheet mixed with naturally activated carbon is an endothermic phenomenon involving physical adsorption. [ABSTRACT FROM AUTHOR]

This Special Issue includes 12 research papers on the development of various materials for adsorbing different contaminants in water, such as Sb, Cr(VI), Cu(II), Zn(II), fluorine, phenol, dyes (indigo carmine, Congo red, methylene blue, and crystal violet), and drugs (dlevofloxacin, captopril, and diclofenac, and paracetamol). The commercial, natural, and synthetic materials used as adsorbents comprise commercial activated carbon, natural clay and montmorillonite, biosorbent based on sugarcane bagasse or algal, graphene oxide, graphene oxide-based magnetic nanomaterial, mesoporous Zr-G-C3N4 nanomaterial, nitrogen-doped core–shell mesoporous carbonaceous nano-sphere, magnetic Fe-C-N composite, polyaniline-immobilized ZnO nanorod, and hydroxy-iron/acid–base-modified sepiolite composite. Various operational conditions are evaluated under batch adsorption experiments, such as pH, NaCl, solid/liquid ratio, stirring speed, contact time, solution temperature, initial adsorbate concentration. The re-usability of laden materials is evaluated through adsorption–desorption cycles. Adsorption kinetics, isotherm, thermodynamics, and mechanisms are studied and discussed. Machine learning processes and statistical physics models are also applied in the field of adsorption science and technology. [ABSTRACT FROM AUTHOR]

Building an optical filtration function into a microfluidic chip is a promising way of simplifying the optical detection system of a microfluidic device. In this paper, a PDMS microfluidic chip filter that is capable of transmitting chlorophyll fluorescence and blocking interfering light in the visible wavelength range was developed for living algae detection with a smartphone. The chip was fabricated by sealing a layer of crystal violet solution in a PDMS layer on the top of the Sudan II-doped PDMS slab, which has a straight microchannel. Optimum dye concentrations and thicknesses for the crystal violet solution layer and Sudan II-doped PDMS slab were investigated and determined by spectrum measurements. It was found that the cut-on range of this integrated microfluidic chip is extended to about 625 nm and the transmittance in the chlorophyll fluorescence range (650 nm to 710 nm) is as high as 95%, when 25 mg L−1 Sudan II-doped PDMS slab (with a 3 mm thickness) and 2 mg L−1 crystal violet solution (with a 0.3 mm thickness) were used. Living algae detection using this chlorophyll-fluorescence-filtering PDMS microfluidic chip and a smartphone-based imaging platform was achieved, and the results compared favorably with those using a commercial filter. [ABSTRACT FROM AUTHOR]

Metals-loaded (Fe 3+ , Cu 2+ and Zn 2+ ) activated carbons (M@AC) with different loading ratios (0.1%, 0.5%, 1%, 5% and 10%) were prepared and employed for catalytic degradation of dye model compounds (crystal violet (CV) and methyl orange (MO)) in wastewater by heterogeneous Fenton-like technique. Compared with Cu@AC and Zn@AC, 0.5% Fe 3+ loaded AC (0.5Fe@AC) had better catalytic activity for dyes degradation. The effects of dyes initial concentration, catalyst dosage, pH and hydrogen peroxide (H 2 O 2 ) volume on the catalytic degradation process were investigated. Cyclic performance, stability of 0.5Fe@AC and iron leaching were explored. Degradation kinetics were well fitted to the pseudo-second-order model (Langmuir-Hinshelwood). Almost complete decolorization (99.7%) of 400 mg L -1 CV was achieved after 30 min reaction under the conditions of CV volume (30 mL), catalyst dosage (0.05 g), H 2 O 2 volume (1 mL) and pH (7.7). Decolorization of MO reached 98.2% under the same conditions. The abilities of pyrolysis char (PC) of dyeing sludge (DS) and metal loaded carbon to remove dye pollutants were compared. The intermediate products were analyzed and the possible degradation pathway was proposed. This study provided an insight into catalytic degradation of triphenylmethane- and aromatic azo-based substances, and utilization of sludge char., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

Six monomeric (1a-1f) and five dimeric (2a-2e) derivatives of the triphenylmethane dye crystal violet (CV) have been prepared. Evaluation of the binding of these compounds to CT DNA by competitive fluorescent intercalator displacement (FID) assays, viscosity experiments, and UV and CD spectroscopy suggest that monomeric derivative 1a and dimeric derivative 2d likely associate with the major groove of DNA, while dimeric derivatives 2a and 2e likely associate with the minor groove of DNA. Additional evidence for the groove occupancy assignments of these derivatives was obtained from ITC experiments and from differential inhibition of DNA cleavage by the major groove binding restriction enzyme BamHI, as revealed by agarose gel electrophoresis. The data indicate that major groove ligands may be optimally constructed from dye units containing a sterically bulky 3,5-dimethyl-N,N-dimethylaniline group; furthermore, the groove-selectivity of olefin-tethered dimer 2d suggests that stereoelectronic interactions (n → π*) between the ligand and DNA are also an important design consideration in the crafting of major-groove binding ligands., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The present study is devoted to the removal of crystal violet dye using the synthesized barium alginate/carbon composites abbreviated as BA (barium alginate), BAAC (barium alginate/activated carbon), BASC (barium alginate/starch carbon), and BASSC (barium alginate/starch carbon modified with CTAB). The adsorptive removal of crystal violet as a function of contact time, pH of solution, composite dose, initial dye concentration, and temperature was studied. The uptake of crystal violet (CV) dye for the composites was recorded in the range of 36 mg g -1 to 50 mg g -1 at pH 8.03 ± 0.03 for an equilibrium time of 120 min. The adsorption kinetics and isotherms in compliance with the CV sorption onto BA/carbon composites corroborated the utmost fit of pseudo-second-order and Freundlich isotherm models, respectively. The recycling process was achieved using the barium alginate-treated bead carbons for different initial CV dye concentrations of 10-30 mg L -1 with a scope of zero disposal. The practicability of BA/carbon composites in a groundwater sample spiked with 30 mg L -1 of CV was successfully achieved with a removal efficiency of about 65-74%. Characterization studies for the composites using FTIR, SEM (with EDS), XRD, TGA, and BET were carried out and discussed in the paper., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Environmental monitoring, environmental remediation, microbiotechnology, wastewater treatment, modeling design Meanwhile, other papers also included the studies on modeling design, pollutant degradation and greenhouse gas emissions, which also covered water, soil and constructed wetlands involved with microorganisms. Keywords: environmental monitoring; environmental remediation; microbiotechnology; wastewater treatment; modeling design EN environmental monitoring environmental remediation microbiotechnology wastewater treatment modeling design 1 3 3 05/17/22 20220513 NES 220513 With the continuous improvement of the level of scientific and technological innovation, many emerging materials and chemicals have come into our lives, which has brought great pressure to the environment and caused an increasing number of contamination problems (Atashgahi et al., [2]; Escher Beate et al., [3]; Johnson Andrew et al., [4]). [Extracted from the article]

The present paper focused on synthesizing a polyacrylamide-titanium dioxide (PAA@TiO2) nanocomposite using a cross-linking method with N, N′-methylenebisacrylamide and then using this composite to eliminate crystal violet (CV) dye from water and to characterize the adsorbent by XRD, FT-IR, and SEM-EDX techniques. The characterization revealed that TiO2 nanoparticles dispersed homogeneously within the polymer matrix. The maximum amount of adsorption was about 38.9 mg g−1 under the adsorbent dose of 5 g L−1, 500 mg L−1 CV dye concentration, and pH 6.9. The interaction between the CV molecule and the PAA@TiO2 nanocomposite surface was studied using Monte Carlo (MC) and molecular dynamics (MD) simulations. The negative value of the Eads (− 586.56 kcal mol−1) of the CV molecules onto the PAA@TiO2 nanocomposite surface gives credibility to the experimental results. All obtained results showed that PAA@TiO2 hybrid polymer nanocomposite could be an alternative adsorbent for crystal violet dye removal from wastewater. [ABSTRACT FROM AUTHOR]

This paper's purpose was to evaluate the interaction between three imidazole derivatives, (2-methyl-1H-imidazol-1-yl)methanol (SAM3), 1,1′-methanediylbis(1H-benzimidazole (AM5) and (1H-benzo[d]imidazol-1-yl)methanol 1-hydroxymethylbenzimidazole (SAM5) on the one hand, and sodium dodecyl sulphate (SDS) on the other, as antifungal combinations against Candida spp. Inhibitory activity was assessed using the agar diffusion method and Minimal Inhibitory Concentration (MIC) and showed moderate inhibitory activity of single imidazole derivatives against Candida spp. The mean value of MIC ranged from 200 µg/mL (SAM3) to 312.5 µg/mL (SAM3), while for SDS the MIC was around 1000 µg/mL. When used in combination with SDS, the imidazole derivatives demonstrated an improvement in their antifungal activity. Their MIC decreased over five times for AM5 and over seven times for SAM3 and SAM5, respectively, and ranged from 26.56 µg/mL (SAM3) to 53.90 µg/mL (AM5). Most combinations displayed an additive effect while a clear synergistic effect was recorded in only a few cases. Thus, the FIC Index (FICI) with values between 0.311 and 0.375 showed a synergistic effect against Candida spp. when SDS was associated with SAM3 (three strains), SAM5 (two strains) and AM5 (one strain). The association of imidazole derivatives with SDS led to the increased release of cellular material as well as the intracellular influx of crystal violet (CV), which indicated an alteration of the membrane permeability of Candida spp. cells. This favored the synergistic effect via increasing the intracellular influx of imidazoles. [ABSTRACT FROM AUTHOR]

Escherichia coli is an important bacterium for preventing food poisoning and biofilm infections. The emergence of antibiotic-resistant microorganisms necessitates the development of new antibiotics. The formation of bacterial biofilm is a drug-resistance mechanism utilized by diverse microorganisms. Therefore, it is important to identify compounds that can inhibit biofilm formation and cell survival, without triggering drug resistance. Herein, the antibacterial and antibiofilm activities of 2 types of Thai propolis (collected from Chiang Mai and Chanthaburi) against E. coli were investigated. The antibacterial activity was evaluated using the paper-disc method, while the minimum inhibitory concentration assay was performed using 2-fold serial dilution. Both types of Thai propolis and their isolated compounds showed antibacterial activity against E. coli (minimum inhibitory concentration: 32 µg/mL). The biofilm growth and development were assessed using a crystal violet solution. In particular, the extracts of the Chiang Mai propolis exhibited a significant antibiofilm formation activity against E. coli. Four prenylflavonoids, present in high proportions in the Chiang Mai propolis extracts, inhibited biofilm formation at low concentrations, contributing to the overall antibiofilm activity. These findings indicate that Thai propolis, a natural product, exhibits antibacterial and antibiofilm activities against E. coli. [ABSTRACT FROM AUTHOR]

In this paper, 4‐aminosalicylic acid functionalized multiwalled carbon nanotubes (CNT‐ASA) filled in a mini‐column and attached to a Flow‐injection system for the adsorptive removal of Crystal violet (CV) dye was employed. The remaining CV concentration was detected by a UV‐Visible Spectrophotometric method, which is proposed in this paper. The factors influencing the adsorption and desorption of CV, such as pH, eluent, sample and eluent flow rates were optimized. The optimum pH was 5.5, the eluent selected for desorption was 1 N acetic acid: ethanol (8 : 2), and the sample and eluent flow rate were both 5 mL min−1. Under the optimum conditions, the results obtained showed that CNT‐ASA possessed excellent dye removal efficiency of ∼99 % and adsorption capacity of 440 mg g−1 for CV. The advantage of using the flow‐injection system is the faster adsorption process (in just 1 minute), less amount and high reuse of the nano‐adsorbent, which is better in comparison to the traditional column method. The proposed method was applied on industrial and river water samples and good recovery (99–105 %) was obtained. Hence, it can be concluded that the proposed method is fast, effective, and can be applied on large‐scale wastewater treatment. [ABSTRACT FROM AUTHOR]

In this paper, Fe3O4 magnetic nanoparticles (Fe3O4 NPs) were successfully synthesised and dispersed on alfalfa to prepare Fe3O4/alfalfa nanocomposite for cationic dye removal from aqueous solutions. Characterisation of Fe3O4/alfalfa nanocomposite using FT-IR, FESEM, and EDX analyses showed that the Fe3O4 NPs were excellently dispersed on alfalfa. The results display that the Fe3O4/alfalfa as a green adsorbent have high removal ability for toxic cationic dyes, such as malachite green (MG) and crystal violet (CV). For Fe3O4-alfalfa, the average particle size of nanoparticles on alfalfa (around 20–30 nm) has decreased compared with alone Fe3O4. The experiments showed that the adsorption of dyes onto Fe3O4-alfalfa better described with pseudo-second-order kinetic and Freundlich isotherm models, suggesting the surface heterogeneity of the Fe3O4/alfalfa. Furthermore, Fe3O4-alfalfa with adsorption capacity of 62.68 mgg−1 and 55.12 mgg−1 towards MG and CV, respectively, was comparable with those of the reported adsorbents. The results indicated that the adsorption of both dyes onto Fe3O4-alfalfa was thermodynamically spontaneous and more favourable at lower temperatures. The results also confirmed that the removal of MG and CV by Fe3O4-alfalfa were remarkable after reusing five times. Therefore, the Fe3O4-alfalfa as a green and low-cost nanoadsorbent with an easy synthesis route could be used for purification of water and wastewater contaminated by pollutants. [ABSTRACT FROM AUTHOR]

Copyright of Forensic Science & Technology is the property of Institute of Forensic Science, Ministry of Public Security and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The combination of two compounds with known antimicrobial activity may, in some cases, be an effective way to limit the resistance to antibiotics of specific pathogens. Molecules carrying pyrazole moiety are well known for their bioactive properties and have wide applicability in the medical and pharmaceutical field. Surfactants have, among other useful properties, the ability to affect the growth of microorganisms. The paper reports on the effect of the combination of two pyrazole derivatives, (1H-pyrazol-1-yl) methanol 1-hydroxymethylpyrazole (SAM1) and 1,1′methandiylbis (1H–pyrazol) (AM1), with sorbitan monolaurate (polysorbate 21, Tween 21, T21) on the growth of Gram-positive and Gram-negative bacteria. The results demonstrated a different ability of this combination to inhibit Staphylococcus aureus and Escherichia coli. T21 intensified the inhibitory activity of the pyrazoles to a greater extent in the Gram-negative bacteria compared to the Gram-positive ones, a fact confirmed by time-kill experiments. The experimental data showed that the association of T21 with the pyrazoles led to the increased release of intracellular material and a more intense uptake of crystal violet, which indicates that the potentiation of the antibacterial effect was based on the modification of the normal permeability of bacterial cells. T21 acted as a modulating factor and increased the permeability of the membrane, allowing the accelerated penetration of the pyrazoles inside the bacterial cells. This fact is important in controlling the global increase in microbial resistance to antibiotics and antimicrobials and finding viable solutions to overcome the antibiotic crisis. The paper highlights the possibility of using non-toxic surfactant molecules in antimicrobial combinations with practical applications. This could widen the range of adjuvants in applications which would be useful in the control of resistant microorganisms. [ABSTRACT FROM AUTHOR]

In this paper, the novel ECL sensor of the 6‐methoxychromone (6‐MC)/S2O82− system was designed by using 2‐naphthalene sulfonic acid (2‐NSA) as a co‐reaction accelerator. Fluorescence, ECL spectrum, and cyclic voltammetry (CV) were used to explore extensively the ECL mechanism of the system. It is worth pointing out that 2‐naphthalene sulfonic acid (2‐NSA) was first proposed as a co‐reaction accelerator, reacting with the coreactant K2S2O8 rather than the luminophore, promoting the generation of additional oxidant SO4− from S2O82−, thus amplifying the ECL signal. Furthermore, under the optimal experimental conditions, the high sensitivity of the 2‐naphthalene sulfonic acid (2‐NSA)+6‐methoxychromone (6‐MC)/S2O82− system was realized for the detection of methyl violet (MV) in the linear range of 10−8~10−2 M, with a detection limit of 5.14×10−10 M. In addition, this find offers some guidance for further developing co‐reaction accelerators with excellent performance in the future. [ABSTRACT FROM AUTHOR]

Developing synthetic strategies for smart materials for the adsorption and separation of toxic chemicals is of great importance. Metal–organic frameworks (MOFs) have been proven to be outstanding adsorbent materials that possess excellent pollutant removal performances in wastewater treatment, including dye recycling. In this work, a neutral Cd(II) based 2D framework with a dual ligand strategy involving –OH functionalized 5-hydroxyisophthalic acid (5-OH-H2IPA) and the amide decorated Schiff base ligand (E)-N′-(pyridin-4-ylmethylene)isonicotinohydrazide (L) has been synthesized by different synthetic routes and characterized by various analytical methods. Thus, crystals of {[Cd(5-OH-IPA)(L)]·CH3OH}n synthesized via diffusion (ADES-7D) and the phase pure bulk product synthesized by conventional reflux (ADES-7C) and the mechanochemical grinding method (ADES-7M) have been established using PXRD data of the respective product showing identical simulated SXRD data to those of ADES-7D. The mechanochemically synthesized ADES-7M possesses a better surface area and CO2 adsorption capability compared to ADES-7C, which is also supported by electron microscopy and particle size measurements. Furthermore, ADES-7 can be used as an efficient adsorbent material for the reversible, selective adsorption (42–99%) and separation of the cationic dyes malachite green (MG), methyl violet (MV), methylene blue (MB), and rhodamine B (RhB) from the mixture of cationic/anionic dyes (methyl orange (MO) and bromocresol green (BCG)) in the aqueous phase. Specifically, ADES-7M possesses better dye capture capability compared to ADES-7C, even in the case of the bigger dye RhB with adsorption differences of 2.38 to 1.01 mg g−1, respectively. The dye adsorption kinetics follows pseudo-second-order kinetics, and the dye adsorption isotherm fits well with the Langmuir/Freundlich adsorption isotherm models. The probable mechanism of adsorption involving the supramolecular interaction between the host MOF and the guest dye has also been proposed. [ABSTRACT FROM AUTHOR]

Aeromonas dhakensis possesses dual flagellar systems for motility under different environments. Flagella-mediated motility is necessary for biofilm formation through an initial attachment of bacteria to the surface, but this has not been elucidated in A. dhakensis. This study investigates the role of polar (flaH, maf1) and lateral (lafB, lafK and lafS) flagellar genes in the biofilm formation of a clinical A. dhakensis strain WT187 isolated from burn wound infection. Five deletion mutants and corresponding complemented strains were constructed using pDM4 and pBAD33 vectors, respectively, and analyzed for motility and biofilm formation using crystal violet staining and real-time impedance-based assays. All mutants were significantly reduced in swimming (p < 0.0001), swarming (p < 0.0001) and biofilm formation using crystal violet assay (p < 0.05). Real-time impedance-based analysis revealed WT187 biofilm was formed between 6 to 21 h, consisting of early (6-10 h), middle (11-18 h), and late (19-21 h) stages. The highest cell index of 0.0746 was recorded at 22-23 h and biofilms began to disperse starting from 24 h. Mutants Δmaf1, ΔlafB, ΔlafK and ΔlafS exhibited reduced cell index values at 6-48 h when compared to WT187 which indicates less biofilm formation. Two complemented strains cmaf1 and clafB exhibited full restoration to wild-type level in swimming, swarming, and biofilm formation using crystal violet assay, hence suggesting that both maf1 and lafB genes are involved in biofilm formation through flagella-mediated motility and surface attachment. Our study shows the role of flagella in A. dhakensis biofilm formation warrants further investigations., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The thermal decomposition or even explosion of nitrocellulose during long-term storage is prevented by adding stabilizers to nitrocellulose-based propellants. A series of novel arylmalonamide[70]fullerocyclopropane (3a–c) were synthesized through Bingel reaction. The molecular structures of 3a–c were verified through 1H NMR, 13C NMR, Fourier transform infrared spectroscopy (FT-IR), UV–visible spectroscopy, and mass spectrum. The thermal stability of 3a–c to nitrocellulose was studied by methyl violet paper test and iso-thermogravimetry method, and the results showed that the stability of 3a–c to nitrocellulose was significantly better than that of the [60]fullerene-based stabilizers. The thermal stability of 3a–c to nitrocellulose improved as the increase of the carbon chain length on the p-position of the benzene ring. The effects of 3a–c on the thermal decomposition of nitrocellulose were obtained by differential thermal analysis, and the results showed that the critical temperature of the thermal explosion of nitrocellulose can be increased by 0.1–2.8 °C by 3a–c. The thermal stability of 3a–c to nitrocellulose in adiabatic environment was confirmed by accelerating rate calorimetry. In addition, the stabilization mechanism was studied through ESR and FT-IR, and the results showed that 3a–c can react with nitrogen oxide radicals released by nitrocellulose. These arylmalonamide[70]fullerocyclopropane with excellent thermal stability and strong radical scavenging ability can be used as a promising stabilizer for single and double based propellants. [ABSTRACT FROM AUTHOR]

In this research paper, various formulations of zeolite‐loaded carboxymethyl tamarind kernel gum (CMTKG) based hydrogels were synthesized and utilized as a potential adsorbent for the removal of crystal violet (CV) dye. The swelling capacity of all the synthesized hydrogels was investigated and the composition of hydrogel which exhibited maximum swelling was used for the characterization and dye removal experiment. The CV dye was chosen as a model dye for the dye removal experiment. The structure of zeolite and zeolite embedded hydrogel was elucidated by XRD, FTIR, FE‐SEM, EDX and elemental papping techniques. The adsorption experiment was investigated by varying the CV concentration, amount of hydrogel adsorbent, temperature, pH of the dye solution, adsorption time, and ionic strength. The Langmuir and Freundlich isotherm models were used to fit the adsorption data and it was observed that the data fitted well with the Langmuir model. Moreover, hydrogel's maximum dye adsorption efficiency was found at 123.60 mg g−1. The adsorption kinetic studies were followed by pseudo‐ first‐order and intraparticle diffusion kinetic models. In addition, regeneration studies were performed for the best adsorbent hydrogel using ethanol solvent and the result concluded the desorption efficiency of hydrogel (82 %) over four desorption cycles. [ABSTRACT FROM AUTHOR]

An excessive accumulation of crystal violet dye in the human body results in an accelerated heart rate, tetraplegia, eye irritation, and long-term damage to the transparent mucous membrane that protects the eyeballs. Accordingly, in this paper, sodium manganese silicate/sodium manganese silicate hydroxide hydrate was easily fabricated as a novel type of nanostructures for the successful disposal of crystal violet dye from aqueous solutions. The formed sodium manganese silicate/sodium manganese silicate hydroxide hydrate nanostructures after the hydrothermal treatment of the gel produced from the interaction of Mn(II) ions with Si(IV) ions at 180 °C for 6, 12, 18, and 24 h were abbreviated as MS1, MS2, MS3, and MS4, respectively. The XRD showed that the average crystallite size of the MS1, MS2, MS3, and MS4 samples is 8.38, 7.43, 4.25, and 8.76 nm, respectively. The BET surface area of the MS1, MS2, MS3, and MS4 samples is 41.58, 46.15, 58.25, and 39.69 m2/g, respectively. The MS1, MS2, MS3, and MS4 samples consist of spherical and irregular shapes with average grain sizes of 157.22, 88.06, 43.75, and 107.08 nm, respectively. The best adsorption conditions of the crystal violet dye employing the MS1, MS2, MS3, and MS4 products were achieved at pH = 8, contact time = 140 min, and solution temperature = 298 kelvin. The linear pseudo-2nd-order model as well as the linear Langmuir isotherm better describe the disposal of the crystal violet dye using the MS1, MS2, MS3, and MS4 adsorbents. The studied thermodynamic parameters indicated that the disposal of the crystal violet dye employing the MS1, MS2, MS3, and MS4 adsorbents is spontaneous, exothermic, and chemical. The maximum disposal capacities of the MS1, MS2, MS3, and MS4 adsorbents towards crystal violet dye are 342.47, 362.32, 411.52, and 310.56 mg/g, respectively. [ABSTRACT FROM AUTHOR]

Microscopic filamentous fungi are ubiquitous microorganisms that adapt very easily to a variety of environmental conditions. Due to this adaptability, they can colonize a number of various surfaces where they are able to start forming biofilms. Life in the form of biofilms provides them with many benefits (increased resistance to desiccation, UV radiation, antimicrobial compounds, and host immune response). The aim of this study is to find a reliable and reproducible methodology to determine biofilm growth of selected microscopic filamentous fungi strains. Several methods (crystal violet staining, MTT assay, XTT assay, resazurin assay) for the determination of total biofilm biomass and its metabolic activity were tested on four fungi - Alternaria alternata, Aspergillus niger, Fusarium culmorum and Fusarium graminearum, and their biofilm was also imaged by spinning disc confocal microscopy using fluorescent dyes. A reproducible biofilm quantification method is essential for the subsequent testing of the biofilm growth suppression using antifungal agents or physical methods. Crystal violet staining was found to be a suitable method for the determination of total biofilm biomass of selected strains, and the MTT assay for the determination of metabolic activity of the biofilms. Calcofluor white and Nile red fluorescent stains successfully dyed the hyphae of microscopic fungi., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

This document is a corrigendum for an article titled "Pien Tze Huang inhibits hypoxia-induced epithelial-mesenchymal transition in human colon carcinoma cells through suppression of the HIF-1 pathway." The authors of the article realized that they had uploaded an incorrect figure for Figure 3A, which showed an overlap of data with Figure 4A. They requested a correction, and the corrected version of Figure 3, showing the correct data for the Hypoxia + PZH experiments, is provided. The authors apologize for any inconvenience caused and state that this error did not affect the overall conclusions of the paper. [Extracted from the article]

Silver chalcogenide quantum dots (QDs) are potential nanosensors for biological and environmental applications. These QDs present low toxicity and their narrow band gap makes them promising as near-infrared (NIR) photoluminescence (PL) probes, exhibiting images with higher penetrability. In addition, hydrophilicity is essential for applications in biological systems as well as detection in aqueous media. Using the same methodology, variations in synthesis conditions can alter the efficiency and performance of their intrinsic properties. Most studies seek the best conditions for each experimental variable in a univariate manner; however, multivariate strategies are a faster and more economical way to achieve this goal. Thus, in this work, we utilized chemometric approaches to enhance the NIR-II PL properties of Ag2Se QDs stabilized with 3-mercaptopropionic acid (MPA). Three experimental designs were used, totaling 58 syntheses, showing that the Ag2Se–MPA QDs, obtained under the conditions of [Ag+] of 2.5 mmol L−1, Ag : Se molar ratio of 8 : 1, MPA : Ag molar ratio of 6 : 1, heating at 70 °C, pH 10, and 180 min, presented the best emission profile with a maximum at 1070 nm and a FWHM of approximately 140 nm. The nanocrystals presented an average diameter of 6 nm and the orthorhombic crystalline phase. Preliminary surface-enhanced infrared absorption (SEIRA) spectroscopy assays were carried out for the detection of methyl violet 2B (MV) dye using these QDs. The enhancement factor obtained was higher than 3.5, which is comparable to those observed for other systems, namely Ag2Se-MSA QDs. These results showed the potential of the Ag2Se–MPA QDs for (bio)sensing applications. [ABSTRACT FROM AUTHOR]

Zinc metal–organic frameworks (Zn-MOFs) of phthalic acid (ZnPA) and nitro-phthalic acid (ZnNPA) microcrystalline particles were fabricated and utilized for the removal of organic cationic dyes (crystal violet (CV), methylene blue (MB) and rhodamine B (RhB)) from water. PXRD studies confirmed the formation of crystalline materials, and BET indicated the mesoporous structure. HR-SEM studies showed the rod and plate morphologies for ZnPA and ZnNPA, respectively. ZnPA revealed low adsorption of dyes (CV, 20%) whereas ZnNPA showed significantly enhanced dye adsorption (CV, 99%). In particular, ZnNPA exhibited higher adsorption of CV (99%) and MB dye (83%) compared to RhB (54%). Nevertheless, ZnNPA could not be reused due to strong adsorption of dyes. Hence, a natural binder was introduced by dipping ZnNPA into tea extract, which also showed high adsorption of CV and MB dyes. Kinetics of adsorption exhibited best fitting with the pseudo-second-order model, indicating strong interactions between the dyes and adsorbent. Adsorption isotherm fitting suggested a good correlation coefficient (R2) with the Freundlich model, suggesting multi-layer adsorption. Interestingly, ZnNPA showed high adsorption of CV and MB dyes across the pH range between 3.0 and 11.0. The binder-introduced ZnNPA adsorbent was easily regenerated and demonstrated three cycles of reusability without significant change in the dye adsorption. Thus, the present work indicated the role of functional groups in the ligand and binder for improving the dye adsorption characteristics of MOFs. [ABSTRACT FROM AUTHOR]

Three-dimensional iodoargentate hybrids [Co(en)3(Ag2I4)]n (1), [Fe(en)3(Ag2I4)]n (2) (en = ethylenediamine) and [Co(dien)2(Ag2I4)]n·nH2O (3) (dien = diethylenetriamine) were prepared in C2H5OH solvent via a one-step reaction under solvothermal conditions. In compounds 1 and 2, AgI4 tetrahedra were interlinked via corner-sharing to form a 3D α-Ag2I4 framework with interpenetrated channels with cross sectional dimensions of 8.071 Å × 9.039 Å and 9.039 Å × 9.039 Å. The AgI4 tetrahedra in compound 3 were connected via both corner- and edge-sharing into a 3D β-Ag2I4 framework with dimensions of 5.929 Å × 8.329 Å, and 8.329 Å × 9.910 Å. Compounds 1–3 showed sensitive photocurrent response under visible light irradiation with steady current densities in the range of 3.46–8.26 μA cm−2. These compounds were catalytically active during the photodegradation of crystal violet (CV), with degradation conversions of 72.2%, 91.5% and 80.1% after 105 min of light irradiation over compounds 1–3, respectively. [ABSTRACT FROM AUTHOR]

Harnessing solar energy using semiconductor-based materials to generate charge pairs to effectively drive photo-redox reactions has been envisioned as a promising approach toward a sustainable future. In this arena, the metal sulfide nanoparticles have demonstrated excellent performance in photomineralizing colored matter. However, their small surface area and relatively slow charge transfer has limited their practical applications. Therefore, for the effective mineralization of colored matter, we devise and construct the Sn2S3–In2S3 S-scheme in collaboration with 2D graphene oxide nanosheets. The material offers a well-defined nanosheet and nanoflake morphology for the effective contact with and catalysis of crystal violet (CV) dye as a model contaminant. Compared to Sn2S3–In2S3/GO, the pristine Sn2S3 and Sn2S3–In2S3 cause negligible degradation of CV using a visible-light source. This enhanced photocatalysis is supported by the peculiar properties of GO, such as its high surface area, electron-shuttling performance, and ability to prevent charge back-recombination. Under simulated conditions, more than 99% of CV was mineralized within 60 min of contact time. The photodegradation follows pseudo-first-order kinetics with a rate constant (Kt) = 0.02317 min−1. Furthermore, the photo mineralization of CV dye was thoroughly investigated using the GC-MS technique. More importantly, Sn2S3–In2S3/GO exhibits promising recyclability over multiple degradation cycles. [ABSTRACT FROM AUTHOR]