Search Results (1,194)

Thiosemicarbazones and thiocarbohydrazones are key sulfur-containing organic compounds known for their diverse biological, pharmaceutical, and industrial applications. Beyond their well-established therapeutic potential, their strong chelating ability allows them to form stable complexes with transition metals, enabling uses in catalysis, corrosion inhibition, and dyeing processes. Their structural characteristics and dynamic conformations critically influence both biological activity and industrial performance, making nuclear magnetic resonance (NMR) spectroscopy an indispensable tool for their analysis. This review provides a comprehensive overview of the conformational and functional properties of bioactive thiosemicarbazones and thiocarbohydrazones, with a focus on how experimental NMR techniques are used to investigate their conformational behavior. In addition to experimental findings, available computational data are discussed, offering complementary insights into their structural dynamics. The integration of experimental and theoretical approaches offers a robust framework for predicting the behavior and interactions of these compounds, thereby informing the rational design of novel derivatives with improved functionality. By highlighting key structural features and application contexts, this work addresses a critical gap in the current understanding of these promising agents across both biomedical and industrial domains. Full article

Applying physico-analytical methods to whole hair fibers enables investigation of hair dye performance. Light microscopy, SEM imaging and EDX mapping of intact hair fibers, as well as TEM imaging of microtome cuts, provided insights into the distribution, size, shape and growth patterns of the dyeing species and particles, thus demonstrating the correlation between silver nanoparticles (AgNPs) and dye impression. Yak hair fibers were treated with a polyphenol-containing Reseda luteola L. extract (RE), which had been acidified using either hydrochloric acid (HCl) or citric acid (CA), and subsequently exposed to silver nitrate (AgNO₃), resulting in the formation of quasi-spherical silver nanoparticles (AgNPs) that were depicted several microns deep inside the hair fiber, regardless of the additive used. The particles appeared to aggregate preferentially in sulfur-rich domains within the hair fiber, probably due to the affinity of silver ions on the NP’s surface towards sulfur. The additives significantly affected the size and aggregation behavior of the particles. Using HCl, larger, aggregated particles were formed, whereas the application of CA yielded smaller, more uniform particles and a higher penetration depth. Despite different particle sizes, the dye outcome was comparable. In strands treated with HCl, washing brought the particles deeper into the hair cortex and resulted in further aggregation. Thus, HCl promoted the formation of larger particles whereas CA yielded more uniformly sized particles. These findings open a new route for metal nanoparticle-based hair dyes with excellent wash fastness. Full article

This study investigated the aerobic biodecolorization of azo dyes by Shewanella oneidensis MR-1. S. oneidensis MR-1 can rapidly degrade azo dyes under aerobic conditions, even at high concentrations of up to 270 mg/L, demonstrating remarkable dye decolorization capabilities. This decolorization efficiency persists even under high concentrations of oxygen. The introduction of different environmental metal ions led to either inhibitory or stimulatory effects on the decolorization of Methyl Orange and Amaranth. Furthermore, the addition of extracellular electron shuttles and electron scavengers confirmed that dyes were being reduced via electron transfer, and the decolorization capability of S. oneidensis MR-1 correlated with electron density. Our study unveils the rapid degradation ability of S. oneidensis MR-1 for dyes under aerobic conditions, which is closely linked to its electron transfer capacity. This research holds significant implications for a deeper understanding of the biodegradation mechanisms of azo dyes under aerobic conditions. Full article

Polypyrrole, which belongs to the conducting polymer family, has demonstrated profound potential in advanced water purification applications due to its inherent electrical conductivity, environmental stability, and tunable surface chemistry. As a sorbent, PPy exhibits high sorption capacity for aquatic contaminants, including heavy metals, pharmaceutical compounds, and their metabolites, as well as synthetic dyes. The removal efficiency is correlated to a complex interaction mechanism involving electrostatic attractions, redox activity, and π–π stacking. Recent advances have expanded the utility by further developing nanostructured PPy-based (nano)composites, which elevate sorption performance by increasing surface area, mechanical integrity, and selective affinity. In addition, its integration into membrane technologies has enabled the design of an effective filtration system with improved selectivity and regeneration capabilities. Moreover, PPy is effective in electrochemical processes of water treatment, including capacitive deionization and electrochemically assisted sorption, opening novel paths towards energy-efficient pollutant removal. The multifunctionality of PPy as a sorbent material highlights its value as an important material for water treatment, with the capability of extended modification tailored for emerging environmental needs revised in this work. Full article

Water contamination from textile dyes is a major environmental hazard. This is due to the textile industry serving among the biggest manufacturers, thus the extensive usage of these dyes. Several methods for the treatment of these pollutants have been used; however, they have limitations in terms of cost, forming secondary pollution, and effectiveness. Metal oxides such as tin oxide (SnO₂) have been identified as potential photocatalysts for the degradation of these dyes. The potential of SnO₂-based photocatalysts, especially those made using green techniques, has been at the forefront of current research. The physical and optical properties, green synthesis techniques, and photocatalytic uses of SnO₂ NPs are examined. Furthermore, methods to improve photocatalytic effectiveness through the formation of heterostructures are also explored. Lastly, the conclusion and future perspectives of these materials as suitable candidates for water treatment are highlighted. Full article

Industrial wastewater pollution has reached acute levels in the environment; consequently, scientists are developing new sustainable treatment methods. Lignocellulosic biomass (LB) stands as a promising raw material because it originates from agricultural waste, forestry residues, and energy crop production. This review examines the application of nanomaterials derived from lignocellulosic resources in wastewater management, highlighting their distinctive physical and chemical properties, including a large surface area, adjustable porosity structure, and multifunctional group capability. The collection of nanomaterials incorporating cellulose nanocrystals (CNCs) with lignin nanoparticles, as well as biochar and carbon-based nanostructures, demonstrates high effectiveness in extracting heavy metals, dyes, and organic pollutants through adsorption, membrane filtration, and catalysis mechanisms. Nanomaterials have benefited from recent analytical breakthroughs that improve both their manufacturing potential and eco-friendly character through hybrid catalysis methods and functionalization procedures. This review demonstrates the ability of nanomaterials to simultaneously turn waste into valuable product while cleaning up the environment through their connection to circular bioeconomic principles and the United Nations Sustainable Development Goals (SDGs). This review addresses hurdles related to feedstock variability, production costs, and lifecycle impacts, demonstrating the capability of lignocellulosic nanomaterials to transform wastewater treatment operations while sustaining global sustainability. Full article

Metal–organic frameworks (MOFs) have emerged as highly versatile materials for the development of next-generation optical biosensors owing to their tunable porosity, large surface area, and customizable chemical functionality. Recently, MOF-based platforms have shown substantial potential in various optical transduction modalities, including fluorescence, luminescence, and colorimetric sensing, enabling the highly sensitive and selective detection of biological analytes. This review provides a comprehensive overview of recent advancements in MOF-based optical biosensors, focusing on their applications in pathogen detection and environmental monitoring. We highlight key design strategies, including MOF functionalization, hybridization with nanoparticles or dyes, and integration into microfluidic and wearable devices. Emerging methods, such as point-of-care diagnostics, label-free detection, and real-time monitoring, are also discussed. Finally, the current challenges and future directions for the practical deployment of MOF-based optical biosensors in clinical and field environments are discussed. Full article

Accurate intraoperative localization of deep-seated lesions remains a major challenge in minimally invasive procedures such as laparoscopic and robotic surgeries. Current marking strategies—including ink tattooing and metallic clips—are limited by dye diffusion, or poor intraoperative visibility. To address these issues, we developed and evaluated four thermosensitive injectable hydrogel systems incorporating indocyanine green-human serum albumin (ICG-HSA) complexes: (1) hexanoyl glycol chitosan (HGC), (2) Pluronic F-127, (3) PCL–PEG–PCL, and (4) PLA–PEG–PLA. All hydrogel formulations exhibited sol–gel transitions at physiological temperatures, facilitating in situ dye entrapment and prolonged fluorescence retention. In vivo fluorescence imaging revealed that HGC and Pluronic F-127 hydrogels retained signals for up to five and two days, respectively. In contrast, polyester-based hydrogels (PCL–PEG–PCL and PLA–PEG–PLA) preserved fluorescence for up to 21–30 days. PLA–PEG–PLA showed the highest signal-to-background ratios and sustained intensity, while PCL–PEG–PCL also achieved long-term retention. These findings suggest that thermosensitive hydrogels incorporating ICG-HSA complexes represent promising tissue marker platforms for real-time, minimally invasive, and long-term fluorescence-guided lesion tracking. Full article

Sulfate radical-based advanced oxidation processes (AOPs) are effective for removing organic pollutants from wastewater. In this study, transition metal-doped cobalt oxyhydroxide (CoOOH) was synthesized as an efficient peroxymonosulfate (PMS) activator for the decolorization of rhodamine B. Doping CoOOH with transition metals enhanced its PMS activation performance compared with that of pure CoOOH. Notably, the reaction rate constant in the Ni-CoOOH/PMS system was approximately 4.3 times higher than that in the CoOOH/PMS system. The presence of multiple metals in the catalyst facilitated efficient Co²⁺/Co³⁺ redox cycling, resulting in improved PMS activation and more effective organic pollutant removal. This study highlights the potential of CoOOH-based materials for use in environmental remediation technologies utilizing PMS. Full article

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

Hydrogels exhibit remarkable physicochemical properties, including high water absorption and retention capacities, as well as controlled release behavior. Their inherent biodegradability, biocompatibility, and non-toxicity make them suitable for a wide range of applications. Cellulose, a biodegradable, renewable, and abundantly available polysaccharide, is a viable source for hydrogel preparation. Ionizing radiation, using electron-beam (EB) or gamma (γ) irradiation, provides a promising approach for synthesizing hydrogels. This study reviews recent advancements in cellulose-based hydrogels, focusing on cellulose and its derivatives, brief information regarding ionizing radiation, comparison between EB and γ-irradiation, synthesis and modification through ionizing radiation technology, and their environmental and agricultural applications. For environmental remediation, these hydrogels have demonstrated significant potential in water purification, particularly in the removal of heavy metals, dyes, and organic contaminants. In agricultural applications, cellulose-based hydrogels function as soil conditioners by enhancing water retention and serving as carriers for agrochemicals. Full article

A metal-ion-free method was developed to prepare κ-carrageenan/cellulose hydrogel beads for efficient cationic dye removal. The beads were fabricated using a mixture of 1-ethyl-3-methylimidazolium acetate and N,N-dimethylformamide as the solvent system, followed by aqueous ethanol-induced phase separation. This process eliminated the need for metal-ion crosslinkers, which typically neutralize anionic sulfate groups in κ-carrageenan, thereby preserving a high density of accessible binding sites. The resulting beads formed robust interpenetrating polymer networks. The initial swelling ratio reached up to 28.3 g/g, and even after drying, the adsorption capacity remained over 50% of the original. The maximum adsorption capacity for crystal violet was 241 mg/g, increasing proportionally with κ-carrageenan content due to the higher surface concentration of anionic sulfate groups. Kinetic and isotherm analyses revealed pseudo-second-order and Langmuir-type monolayer adsorption, respectively, while thermodynamic parameters indicated that the process was spontaneous and exothermic. The beads retained structural integrity and adsorption performance across pH 3–9 and maintained over 90% of their capacity after five reuse cycles. These findings demonstrate that κ-carrageenan/cellulose hydrogel beads prepared via a metal-ion-free strategy offer a sustainable and effective platform for cationic dye removal from wastewater, with potential for heavy metal ion adsorption. Full article

The contamination of water bodies by industrial dyes poses a significant environmental challenge on a global scale. Conventional wastewater treatment methods often suffer from limitations related to high cost, limited efficiency, and potential secondary environmental impacts. Recent advances in photocatalytic technologies have highlighted the potential of metal sulfide-based photocatalysts, particularly those synthesized through environmentally friendly, plant-mediated approaches, as promising alternatives for efficient and sustainable dye degradation. However, despite their promising potential, metal sulfide photocatalysts often suffer from limitations such as photocorrosion, low stability under irradiation, and rapid recombination of charge carriers, which restrict their long-term applicability. In light of these challenges, this review provides a comprehensive examination of the physicochemical characteristics, synthetic strategies, and photocatalytic applications of metal sulfides. Particular emphasis is placed on green synthesis routes employing plant-derived extracts, which offer environmentally benign and sustainable alternatives to conventional methods. Moreover, the review elucidates various modification approaches, most notably, the formation of heterostructures, as viable strategies to enhance photocatalytic efficiency and mitigate the aforementioned drawbacks. The green synthesis of metal sulfides, aligned with the principles of green chemistry, offers a promising route toward the development of sustainable and environmentally friendly water treatment technologies. Full article

This review critically examines the recent advancements in the development and application of electrospun molecularly imprinted polymer (MIP) nanofiber membranes for environmental remediation. Emphasizing the significance of these materials, the discussion highlights the mechanisms by which electrospun MIPs achieve high selectivity and efficiency in removing various pollutants, including dyes, heavy metals, and pharmaceutical residues such as NSAIDs and antiretroviral drugs. The synthesis methodologies are explored in detail, focusing on the choice of monomers, templates, and polymerization conditions that influence the structural and functional properties of the membranes. Characterization techniques used to assess morphology, surface area, porosity, and imprinting efficacy are also examined, providing insights into how these parameters affect adsorption performance. Furthermore, the review evaluates the performance metrics of electrospun MIPs, including adsorption capacities, selectivity, reusability, and stability in complex environmental matrices. Practical considerations, such as scalability, regeneration, and long-term operational stability, are discussed to assess their potential for real-world applications. The article concludes with an outline of future research directions, emphasizing the need for multi-template imprinting, integration with existing treatment technologies, and field-scale validation to address current limitations. Full article

Nanostructure-based coloration has been investigated extensively to overcome the limitations of conventional pigments and dyes. In this study, we focused on the dynamic coloration of plasmonic structures via the photothermal deformation of a metal semi-shell. However, identifying the optimal structure using this method typically requires considerable computational time. To address the high computational cost of structural optimization in dynamic plasmonic coloration, we propose an efficient method for estimating the optimal nanostructure geometry. The color gamut area was found to be influenced by both the nanosphere density and the thickness of the metal semi-shell. The optical response of deformed semi-shells, resulting from laser-induced local heating, was simulated across a range of semi-shell shapes. From these simulations, an empirical correlation was identified that links nanoparticle diameter, density, and semi-shell thickness. This correlation enables the rapid estimation of optimal parameters, thereby reducing computational demands and supporting the efficient fabrication of dynamic plasmonic color materials. Full article