Search Results (648)

A novel near-infrared (NIR) squaraine-based chemosensor, SQ-68, has been designed and synthesized for the sensitive and selective detection of Cu²⁺ and Ag⁺ ions, offering a compact solution for multi-analyte sensing. SQ-68 demonstrates high selectivity, with its performance influenced by the solvent environment: It selectively detects Cu²⁺ in acetonitrile and Ag⁺ in an ethanol–water mixture. Upon binding with either ion, SQ-68 undergoes significant absorption changes in the NIR region, accompanied by visible color changes, enabling naked-eye detection. Spectroscopic studies confirm a 1:1 binding stoichiometry with both Cu²⁺ and Ag⁺, accompanied by hypochromism. The detection limits are 0.09 μM for Cu²⁺ and 0.38 μM for Ag⁺, supporting highly sensitive quantification. The sensor’s practical applicability was validated in real water samples (sea, lake, and tap water), with recovery rates ranging from 73–95% for Cu²⁺ to 59–99% for Ag⁺. These results establish SQ-68 as a reliable and efficient chemosensor for environmental monitoring and water quality assessment. Its dual-analyte capability, solvent-tunable selectivity, and visual detection features make it a promising tool for rapid and accurate detection of heavy metal ions in diverse aqueous environments. Full article

Rationally designing and synthesizing chemosensors capable of simultaneously detecting both anions and cations via water content modulation is challenging. In this study, we synthesized and characterized a novel triazine calixarene derivative-based iodide and copper ion-selective fluorescent “turn-off” sensor. This dual-channeled fluorescent probe is able to recognize Cu²⁺ and I⁻ ions simultaneously in aqueous systems. The fluorescent sensor s4 was synthesized by displacement reaction of acridine with 1, 3-bis (dichloro-mono-triazinoxy) benzene in acetonitrile. Mass spectrometry (MS), UV-vis, and fluorescence spectra were acquired to characterize the fluorescence response of s4 to different cations and anions, while infrared (IR) spectroscopy and isothermal titration calorimetry (ITC) were employed to study the underlying selectivity mechanism of s4 to Cu²⁺ and I⁻. In detail, s4 displayed extremely high sensitivity to Cu²⁺ with over 80% fluorescence decrement caused by the paramagnetic nature of Cu²⁺ in the aqueous media. The reversible fluorescence response to Cu²⁺ and the responses to Cu²⁺ in the solution of other potential interferent cations, such as Li⁺, Na⁺, K⁺, Ca²⁺, Cd²⁺, Zn²⁺, Sr²⁺, Ni²⁺, Co²⁺ were also investigated. Probe s4 also exhibited very good fluorescence selectivity to iodide ions under various anion (F⁻, Cl⁻, Br⁻, NO₃⁻, HSO₄⁻, ClO₄⁻, PF₆⁻, AcO⁻, H₂PO₄⁻) interferences. In addition to the fluorescent response to I⁻, s4 showed a highly selective naked-eye-detectable color change from colorless to yellow with the other tested anions. Full article

Eugenol-based azo dyes illustrate how bio-sourced compounds like eugenol can be transformed through synthetic processes into functional and colorful compounds. The main purpose of the present work was to develop new responsive colorimetric sensors for metal cations based on eugenol-derived azo compounds. The incorporation of the azo group into the eugenol framework allows for strong electronic interactions with metal cations, leading to distinct color changes observable to the naked eye. These azo-eugenol dyes exhibit shifts in their UV-Vis absorption spectra upon complexation with metal cations such as copper (Cu²⁺) and lead (Pb²⁺), making them effective sensors for environmental and analytical applications. The eugenol-based azo dyes were subjected to photophysical studies to understand selectivity, response time, and stability in relation to metal cations, which will be a starting point for the monitoring of toxic metal contaminants in aqueous environments. Full article

In recent decades, there has been an increase in the development of non-invasive and non-destructive analytical techniques in the field of cultural heritage. The present study aims to characterize the frescoes in the hypogeum environment of the San Pietro a Corte complex in Salerno (Campania, Italy) through a multi-analytical approach that couples Infrared Reflectography with X-Ray Fluorescence Spectrometry. Thermographic and hygrometric measurements were also performed to evaluate their state of conservation in relation to environmental parameters such as relative humidity and temperature at the frescoed walls. Spectroscopic investigations revealed a predominant use of natural pigments—chiefly iron-rich earths—and uncovered details invisible to the naked eye that aid art historians in refining stylistic attributions. Hygrometric data showed that the central zones of the frescoes retain the highest moisture levels, underscoring the need for a carefully tailored conservation plan. Overall, this multi-analytical methodology provides important information that enables conservators and restorers to understand both the materials and the preservation requirements of these artworks from a scientific and conservation perspective. Full article

Among European colubroids, scale sensilla—mechanoreceptors present in the head integument—are more expressed in natricids. The presence of protruded sensilla, observable with the naked eye, is found in the cephalic shields of all species belonging to the genus Natrix. The identification of these sense organs in this genus determines its correlation in aquatic and semi-aquatic species, in which these traits are more developed and recognizable than in terrestrial species. As hypothesized for elapoids, this differentiation could be due to the fact that in natricids, like sea snakes, these can perform a hydrodynamic function in addition to the mechanosensory one. In support of this thesis, within the genus Natrix, the most aquatic species of the five, Natrix tessellata, features the most expressed sensilla. This specificity represents a further analogy in the evolutionary convergences involving the cephalic region that this species shares with marine elapids. Still in the genus Natrix, a second trait involving the shields has been identified, expressing itself in the opposite condition to the protruded sensilla, occurring as a pitting arranged mainly within the shields along the upper portion of the labial arches. In vivo examinations and microscopy were performed on different species of the Natrix genus, and comparative analyses have been carried out on other natricid taxa from the New and Old World, where the presence of protruded scale sensilla has been found in several species. Full article

Urban sewage, aquaculture wastewater, and medical wastewater are significant reservoirs and transmission sources of Salmonella. Rapid detection of Salmonella is crucial for effectively reducing the risk of disease transmission and safeguarding public health. Differentiating viable Salmonella from inactivated cells presents significant challenges, affecting the accurate assessment of pathogen risks. Moreover, current detection methods face several limitations, including lengthy detection periods, high costs, and limited applicability, underscoring the need for rapid, sensitive, and visual detection diagnostic approaches. In this study, we combined propidium monoazide (PMA) with recombinase polymerase amplification (RPA) and clustered regularly spaced short palindromic repeats (CRISPR)/Cas12a systems to develop a rapid detection system for viable Salmonella targeting the fimY gene. DNA of viable Salmonella was amplified and visually detected within 60 min and dead cells were effectively excluded. We assessed the specificity and sensitivity of the PMA-RPA-CRISPR/Cas12a assay. The results showed that the assay had a high level of specificity, with no reactions observed with other pathogens. The application of PMA has no effect on the sensitivity of RPA-CRISPR/Cas12a technology and the visibility of the fluorescence reporting system. We successfully detected viable Salmonella in wastewater with a minimum detection limit of 10¹ CFU/mL. In summary, the PMA-RPA-CRISPR/Cas12a system developed in this study allows for the rapid and visual detection of viable Salmonella in wastewater at concentrations as low as 10¹ CFU/mL. By integrating PMA with the RPA-CRISPR/Cas12a technology, this system offers valuable technical support for the efficient, sensitive, and clear detection of viable Salmonella in wastewater. Full article

The reaction of PtCl₂ with a PNN type ligand dppmaphen (N-(diphenylphosphanylmethyl)-2-amino-1,10-phenanthroline) yielded a new Pt(II) complex [Pt(dppmaphen)Cl]Cl·H₂O (1). Upon excitation at 370 nm, compound 1 emits yellow phosphorescence at 539 and 576 nm at room temperature. Exposure of compound 1 to MeOH vapor induces a shift in its emission to 645 nm, which can be attributed to the substitution of MeOH molecules for H₂O, resulting in the disruption and reorganization of weak interactions in 1. This response is selective for MeOH and, to a lesser extent, EtOH, the orange photoluminescence recovered in air. The emission change of 1 was reversible and visible to the naked eye. Full article

The selection of the peak power of a photovoltaic system to meet the energy demand of a building is a key task in the energy transformation. This article presents an algorithm for assessing the correctness of the selection of a photovoltaic system with a peak power of 50 kWp for the needs of a university administration building. This is made possible due to the use of an advanced photovoltaic inverter, which is a device of the Internet of Things and the smart metering system. At the beginning of the review, the authors employed the naked eye measurement data of the time series related to the power production by the photovoltaic system and its consumption by the university building. Then, traditional statistical analyses were performed, characterizing the generated power divided into self-consumption power and that fed into the power grid. The analysis of the total consumed power was performed with the division into the power produced by the photovoltaic system and that taken from the power grid. The analyses conducted were subjected to expert validation aimed at explaining the nature of the behavior of the power generation and consumption systems. The main goal of this article is to determine the signatures of the power generated by the photovoltaic system and consumed by the administration building. As a result of unsupervised clustering, the power generation and consumption space were divided into states. These were then termed based on their nature and their usefulness in managing the power produced and consumed. Presentation of clustering results in the form of heatmaps allows for localization of specific states at specific times of the day. This leads to their better understanding and quantification. The signatures of power generated by the photovoltaic system and consumed by the university building confirmed the possibility of using an energy storage system. The presented computational algorithm is the basis for determining the correctness of the photovoltaic system selection for the current energy needs of the building. It can be the basis for further analysis related to the prediction of both the power generated by Renewable Energy Sources and the energy consumed by diverse types of buildings. Full article

Hydrogen chloride (HCl) is one of the most hazardous air pollutants and can cause significant damage to human health and the environment. Therefore, the continuous quantitative monitoring of HCl is of great practical importance. In this work, a novel triphenylamine derivative, named TPTc-DBD, with a Schiff base structure was synthesized. The molecular structure of TPTc-DBD was determined by NMR analysis, FTIR analysis and single crystal diffraction analysis. On this basis, a porous polyvinylidene fluoride (PVDF) film containing TPTc-DBD was then prepared by a spin-coating method, and its sensitivity to HCl was evaluated by naked eye and ultraviolet-visible absorption spectrum, respectively. The detection limit of the composite porous film for HCl molecules was determined to be 5.8 mg/m³. Interestingly, the composite films absorbing HCl can be reactivated by NH₃, which provides a cycle detection ability for HCl. After five testing cycles, the detection error remained below 1%. Furthermore, the microstructure of the film remained unchanged, highlighting its exceptional detection performance for HCl. Full article

The increasing prevalence of antimicrobial-resistant (AMR) bacteria in humans, animals, and the environment underscores the necessity for a rapid, sensitive, and specific method to identify resistance genes. Objectives: This study aims to develop a reliable detection tool for identifying the tetracycline-resistant gene tet(M) in Enterococcus species using a real-time loop-mediated isothermal amplification (RT-LAMP) assay. Real-time visualization through a turbidimeter enabled precise estimation of time-to-positivity for gene detection. Methodology: Six primers were designed using PrimerExplorer v.5, and the assay was optimized across different temperatures and incubation times. Validation was conducted by testing 52 tet(M)-positive clinical enterococci isolates and spiking urine samples from a healthy volunteer and a cow with tet(M)-positive Enterococcus species. Results: The tet(M) gene was detected as early as 33 min, with optimal amplification occurring within 60 min at 60 °C. The assay demonstrated 100% specificity with the established primers. The sigmoidal graphs were corroborated with visual confirmation methods, including a green color change (visible to the naked eye), green fluorescence (under UV light), and a 200 bp PCR product observed via agarose gel electrophoresis. Notably, the tet(M) RT-LAMP assay exhibited a detection limit of 0.001 pg/μL, significantly surpassing conventional PCR, which had a detection limit of 0.1 pg/μL. Conclusions: This rapid, cost-effective, highly sensitive, and specific tet(M) RT-LAMP assay holds significant promise as a surveillance tool for antimicrobial resistance monitoring within a One Health framework, particularly in low-resource countries. Full article

Organophosphate pesticides (OPs) enter the environment through various avenues, posing significant health risks. This highlights the need to monitor OPs in food and environmental samples. This study introduces an enzyme inhibition-mediated distance-based paper (EIDP) biosensor designed for naked-eye visual detection of OPs in food samples. We synthesized a copper alginate (Cu-Alg) hydrogel that traps water within the gel and restricts water flow on pH paper. When incubated with acetylcholinesterase (AChE) and acetylthiocholine (ATCh), the enzyme activity of AChE on ATCh generates thiocholine, which interacts with the Cu²⁺ ions in the gel. This interaction alters the gel’s 3D structure, releasing the trapped water onto the pH paper. Conversely, when AChE is exposed to OPs, its activity is inhibited, limiting the water flow from the gel. As a result, OPs are quantified by measuring the reduction in water flow distance within a linear range of 18 to 105 ng/mL, with a lower detection limit of 18 ng/mL. The EIDP biosensor exhibits high selectivity for OP detection and successfully analyzes OPs in pumpkin and rice samples, achieving percent recoveries ranging from 93% to 103%. This method offers a straightforward, portable, instrument-free, and cost-effective solution for detecting OPs in food samples. Full article

New glasses in the xCdO-(90 − x)TeO₂-10GeO₂ system were obtained by the conventional melt-quenching process at 900 °C. The glasses were transparent to the naked eye. The diffraction patterns indicate that the samples were mostly amorphous, except for the CdO-rich glasses, in which the formation of nanocrystals of CdO and Cd₃TeO₆ were identified. Raman spectroscopy analysis of the samples displayed the existence of TeO₃, TeO₃₊₁, TeO₄, and GeO₄, structural units within the glass matrix. The optical band gap of the glass samples was determined by optical absorption spectroscopy using the Tauc method. Depending on the relative content of TeO₂, their values varied in the range of 2.32–2.86 eV. The refractive index was obtained from the band gap values. The XPS measurements showed that Ge 3d, O 1s and Te 3d_3/2, Te 3d_5/2, Cd 3d_5/2, and Cd 3d_3/2 doublets shifted to higher binding energy values as the amount of TeO₂ was increased. The binding energy values of the Te 3d doublet are related to the TeO₄ and TeO₃ groups. Full article

Marine mammal monitoring, a growing field of research, is critical to cetacean conservation. Traditional ‘tagging’ attaches sensors such as GPS to such animals, though these are intrusive and susceptible to infection and, ultimately, death. A less intrusive approach exploits UUV commanded by a human operator above ground. The development of AI for autonomous underwater vehicle navigation models training environments in simulation, providing visual and physical fidelity suitable for sim-to-real transfer. Previous solutions, including UVMS and L2D, provide only satisfactory results, due to poor environment generalisation while sensors including sonar create environmental disturbances. Though rich in features, image data suffer from high dimensionality, providing a state space too great for many machine learning tasks. Underwater environments, susceptible to image noise, further complicate this issue. We propose SWiMM_2.0, coupling a Unity simulation modelling of a BLUEROV UUV with a DRL backend. A pre-processing step exploits a state-of-the-art CMVAE, reducing dimensionality while minimising data loss. Sim-to-real generalisation is validated by prior research. Custom behaviour metrics, unbiased to the naked eye and unprecedented in current ROV simulators, link our objectives ensuring successful ROV behaviour while tracking targets. Our experiments show that SAC maximises the former, achieving near-perfect behaviour while exploiting image data alone. Full article

In this study, a RGB based ternary-emission molecularly imprinted ratiometric fluorescence (MI-RFL) sensor was facilely constructed by using a post-imprinting mixing strategy for the sensitive detection of enrofloxacin (ENR). Upon excitation at 365 nm, the MI-RFL sensor exhibited significant emission peaks at 450, 550, and 620 nm. As the ENR concentration increased, the blue fluorescence generated by ENR in the sensing system gradually intensified, while the red and green fluorescence emitted by the quantum dots in the molecularly imprinted polymers (MIPs) was significantly quenched. Sensing conditions were systematically investigated, including the excitation wavelength, mixing ratio of red/green MIPs, the pH of the buffer solution, and the reaction time. Under the optimal conditions, the developed sensor showed a good linear relationship within the range of 0.25–4 ppm along with obvious color change, with a low detection limit of 0.134 ppm. High selectivity was also attained with an imprinting factor up to 11.65. When applied to real samples of seawater and seafood, the sensor showed good recovery rates of 94.3–126.4% and accuracy with a relative standard deviation of less than 3.97%. Furthermore, the sensor-based kit was easily fabricated and, thus, naked-eye detection of ENR was realized onsite. This study can provide a universal approach for the rapid and visual detection of ENR in complicated matrices. Full article

The sensing of surfactants is a topic of interest for industrial and environmental purposes. Polydopamine-coated magnetite (Fe₃O₄@PDA) can be a relevant support for the detection of cationic surfactants in water samples. The negative charge in the surface of the PDA material favors the interaction with cationic molecules and allows the design of a chemoreagent for the detection of cationic surfactants by displacement or competition with methylene blue (MB). Magnetite nanoparticles with single and double PDA coating have been prepared and characterized. The PDA surface effectively coats magnetite nanoparticles with a thickness of 5 or 19 nm and a Z potential of −30 mV. The adsorption of MB follows second-order kinetics, and up 33 mg of dye can be loaded in 1 g of the support. The cationic surfactants can displace MB from the Fe₃O₄@PDA surface, coloring the solution. Thus, it can be applied for the analysis of water samples. The system is selective towards cationic molecules with long alkyl chains, but the response is influenced by high concentrations of divalent cations. The material can be used following diverse sensing protocols with a detection range from 4 × 10⁻⁶ to 2 × 10⁻⁴ M. The simplicity of its handling together with the naked eye detection allows its application in kits for field analysis with screening purposes. Full article