Mercury Ions Research Articles

Thiourea Functionalised Receptor for Selective Detection of Mercury Ions and its Application in Serum Sample.

A thiourea functionalised fluorescent probe 1-phenyl-3-(pyridin-4-yl)thiourea was synthesized and utilised as a fluorescent turn-on chemosensor for the selective recognition of Hg2+ ion over competitive metal ions including Na+, Mn2+, Li+, Cr2+, Ni2+, Ca2+, Cd2+, Mg2+, K+, Co2+, Cu2+, Zn2+, Al3+ and Fe2+ ions based on the inter-molecular charge transfer (ICT). Intriguingly, the receptor demonstrated unique sensing capabilities for Hg2+ in DMSO: H2O (10:90, v/v). The addition of Hg2+ ions to the sensor resulted in a blue shift in the absorption intensity and also enhancement in fluorescence intensity at 435nm. Fluorescence emission intensity increased linearly with Hg2+ concentration ranging from 0 to 80 µL. The detection limit and binding constant were determined as 0.134 × 10-6M and 1.733 × 107M-1, respectively. The sensing behavior of Hg2+ was further examined using DLS, SEM and FTIR. The probe could detect Hg2+ ions across a wide pH range. Furthermore, the receptor L demonstrated good sensing performance for Hg2+ in bovine serum albumin and actual water samples.

Developing new Hydrazine Carbothioamide Molecules for Selective Colorimetric/Fluorometric Detection of Environmentally Essential Hg2+ and Ag+ Metal Ions in Mixed Aqueous Media

Developing new Hydrazine Carbothioamide Molecules for Selective Colorimetric/Fluorometric Detection of Environmentally Essential Hg2+ and Ag+ Metal Ions in Mixed Aqueous Media

A highly stable electrochemical sensor with antifouling and antibacterial capabilities for mercury ion detection in seawater

The monitoring of heavy metal ions in ocean is crucial for environment protection and assessment of seawater quality. However, the detection of heavy metal ions in seawater with electrochemical sensors, especially for long-term monitoring, always faces challenges due to marine biofouling caused by the nonspecific adsorption of microbial and biomolecules. Herein, an electrochemical aptasensor, integrating both antifouling and antibacterial properties, was developed for the detection of Hg2+ in the ocean. In this electrochemical aptasensor, eco-friendly peptides with superior hydrophilicity served as anti-biofouling materials, preventing nonspecific adsorption on the sensing interface, while silver nanoparticles were employed to eliminate bacteria. Subsequently, a ferrocene-modified aptamer was employed for the specific recognition of Hg2+, leveraging the aptamer's ability to fold into a thymine-Hg2+-thymine (T-Hg2+-T) structure upon interaction, and bringing ferrocene nearer to the sensor surface, significantly amplifying the electrochemical response. The prepared electrochemical aptasensor significantly reduced the nonspecific adsorption in seawater while maintaining sensitive electrochemical response. Furthermore, the biosensor exhibited a linear response range of 0.01–100 nM with a detection limit of 2.30 pM, and realized the accurate monitoring of mercury ions in real marine environment. The research results offer new insights into the preparation of marine antifouling sensing devices, and it is expected that sensors with antifouling and antimicrobial capabilities will find broad applications in the monitoring of marine pollutants.

Engineering MOF-derived 2D NPC-TiO2 nanotablet/3D marigold-like ZnIn2S4/CdS nanoparticles dual Z-scheme heterojunction with excellent photoelectric performance: A novel material for sensitive and facile photoelectrochemical sensing detection of mercury ions in aqueous environments by ion-exchange sensing strategy

Herein, a new NH2-MIL-125-derived 2D nitrogen-doped porous carbon-titanium dioxide (NPC-TiO2) nanotablet/3D marigold-like ZnIn2S4/CdS nanoparticles (NPs) dual Z-scheme heterojunction was first exploited for photoelectrochemical (PEC) measurement of mercury ions (Hg2+). Taking NH2-MIL-125 as precursor, the 2D NPC-TiO2 nanotablet was prepared by calcination. The 3D marigold-like ZnIn2S4 and CdS NPs were synthesized by hydrothermal method and aqueous synthesis way, respectively. The acquired NPC-TiO2, ZnIn2S4 and CdS were sequentially modified on the indium tin oxide (ITO) electrode to form the PEC sensing interface by layer-by-layer assembly. Due to the matched band-edge levels, and strong light-harvesting ability, the given heterostructure on ITO electrode generated a large photocurrent. Importantly, it was found that 2D NPC-TiO2 nanotablet/3D marigold-like ZnIn2S4/CdS NPs dual Z-scheme heterojunction could show specifically increased photocurrent signal towards to Hg2+ by employing CdS NPs as Hg2+-recognition probe with selective Cd-to-Hg ion-exchange, resulting from the in-situ formation of the new quaternary NPC-TiO2/ZnIn2S4/CdS/HgS heterostructure to further facilitate the spatial transmission and separation of charges. As a result, Hg2+ was highly sensitively detected with a low detection limit of 20 fM. This PEC sensor was also verified by evaluating Hg2+ in tap water, river water and lake water, demonstrating great application prospect for environment pollutant measurement.

Construction of cellulose-based hybrid hydrogel beads containing carbon dots and their high performance in the adsorption and detection of mercury ions in water

Cellulose-based adsorbents have been extensively developed in heavy metal capture and wastewater treatment. However, most of the reported powder adsorbents suffer from the difficulties in recycling due to their small sizes and limitations in detecting the targets for the lack of sensitive sensor moieties in the structure. Accordingly, carbon dots (CDs) were proposed to be encapsulated in cellulosic hydrogel beads to realize the simultaneous detection and adsorption of Hg (II) in water due to their excellent fluorescence sensing performance. Besides, the molding of cellulose was beneficial to its recycling and further reduced the potential environmental risk generated by secondary pollution caused by adsorbent decomposition. In addition, the detection limit of the hydrogel beads towards Hg (II) reached as low as 8.8×10-8 M, which was below the mercury effluent standard declared by WHO, exhibiting excellent practicability in Hg (II) detection and water treatment. The maximum adsorption capacity of CB-50 % for Hg (II) was 290.70 mg/g. Moreover, the adsorbent materials also had preeminent stability that the hydrogel beads could maintain sensitive and selective sensing performance towards Hg (II) after 2 months of storage. Additionally, only 3.3% of the CDs leaked out after 2 weeks of immersion in water, ensuring the accuracy of Hg (II) evaluation. Notably, the adsorbent retained over 80% of its original adsorption capacity after five consecutive regeneration cycles, underscoring its robustness and potential for sustainable environmental applications.

Metal ion-induced multifunctionality in luminescent hydrogels for information encryption and mercury ion detection

Information security has long been a focal point of research. However, the development of cryptographic hydrogels endowed with both high security and multifunctionality remains a challenge. Herein, we reported a method to construct multifunctional hydrogels using a metal ion-induced strategy. Leveraging Au- induced luminescence, Zn2+- induced shape memory, and Hg2+- induced fluorescence quenching, our method engendered a suite of distinctive properties, including fluorescence, shape memory effects, and ionic conductivity. Tunable fluorescence was utilized for detecting Hg2+ with a detection limit as low as 0.0007 μmol/L. Additionally, a successful design of a multilevel information encryption platform, ranging from 2D to 3D, was achieved by combining the aforementioned properties. The information written using Hg2+ as ink can be protected by the fixed shape of Zn2+, and the encrypted information can only be read under the conditions of shape recovery and UV irradiation. This simple yet effective strategy demonstrates a promising future for the application of this hydrogel in information encryption.

Development of a new series of thioacetal based fluorescence chemosensors for highly sensitive determination of Hg2+ in environmental samples and cell imaging

Mercury ion is one of the most harmful metal ions with significant hazards to the environment and human health. Thus, the development of innovative, sensitive, and selective sensors to help address the detrimental impacts of heavy metal contamination is necessary. In this work, we present three new chemosensors based on the deprotection reaction of the thioacetal group for distinguishing Hg2+ in environmental samples. These chemosensors show good photophysical properties with high quantum yield in aqueous medium. These prepared chemosensors were employed as fluorometric sensors for the determination of Hg2+ through the quenching of fluorescence emission due to the Hg2+-induced hydrolysis of the thioacetal to the aldehyde group. In the presence of Hg2+, chemosensors showed an emissive color transformation from blue fluorescence to non-fluorescence under UV light, which was readily seen by the visual eye. These chemosensors also exhibited highly distinctive selectivity toward Hg2+ over other interfering metal ions, with detection limits of 1.1 ppb, 13.4 ppb, and 12.7 ppb. Moreover, the practical applicability of chemosensor was successfully demonstrated in real water samples and herb extract samples.

Novel fluorescent sensor based on triazole-pyridine derivative for selective detection of mercury (II) ions in different real water samples: Experimental and DFT calculations

Toxic heavy metals, particularly mercury II ions, must be selectively detected in industrial effluent to restrict their percentage and thereby aid in environmental protection. The present study describes the synthesis of 6-(4-(4-(5-cyano-6-oxo-4-styryl)-1,6-dihydropyridin-2-yl)-5-methyl-1H-1,2,3-triazol-1-yl)phenyl)-2-oxo-4-styryl)-1,2-dihydropyridine-3-carbonitrile (TOHC) and its ability as a novel selective fluorescent probe for the detection of mercury II ions in different real water samples. The structure of the prepared TOHC was confirmed by both FTIR and 1HNMR analysis, while crystal structure and thermal stability was investigated using XRD and TGA techniques. The optical properties of TOHC were investigated using both UV–vis and fluorescence spectroscopy at different pH values. Its luminescent properties obtained when TOHC is excited by a wavelength equal to 424 nm, where a maximum emission peak has observed at a wavelength equal to 466.6 nm. Moreover, using Stern-Volmer equation indicate that there is a good correlation between the concentration of Hg2+ ions and the fluorescence intensity of TOHC accompanied with high quenching rate equal to 2.24 x 104 mol−1.L. Selectivity of TOHC toward Hg2+ ions was confirmed by the assistance of fifteen different metal cations. In addition, Job’s Plot method and UV–vis spectroscopy were used to estimate the stoichiometry as well as understand the quenching mechanism between TOHC sensor and Hg2+ ions. The applicability of TOHC sensor for the detection of Hg2+ ions in real samples was further validated using five different real water samples and exhibited excellent results. Lastly, DFT calculations were conducted to provide atomistic insights into the chemical interaction between Hg(II) and TOHC.

Electrochemical sensing of Pb2+, Cu2+, and Hg2+ by an aminoclay-based porous covalent organic polymer/ multi-walled carbon nanotubes modified glassy carbon electrode

We present a novel electrochemical sensor for the simultaneous detection of Lead (Pb2+), Copper (Cu2+), and Mercury (Hg2+) ions in seafood samples using differential pulse anodic stripping voltammetry (DPASV) technique. The sensor incorporates an aminoclay-based porous covalent organic polymer (AC-PCOP) derived from the polymerization of aminoclay and 1,3,5-benzenetricarboxylic acid (trimesic acid). To enhance conductivity, the AC-PCOP is combined with multi-walled carbon nanotubes (MWCNTs) and utilized for modifying the surface of the glassy carbon electrode (GCE). The AC-PCOP was characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) analysis, and infrared spectroscopy (IR). These analyses confirmed the presence of a hierarchical architecture in the AC-PCOP, which exhibited a spherical shape. The proposed modifier facilitates the deposition-stripping process and electron diffusion between electrolyte and heavy metal ions. Optimized conditions yielded limit of detections (LODs) of 0.0006, 0.0016, and 0.0003 nM, with linear ranges from 0.002 to 1000 nM, 0.005 to 1000 nM, and 0.001 to 1000 nM for Pb2+, Cu2+, and Hg2+, respectively. The sensor successfully measured these ions in seafood samples. Control experiments and validation were performed using cold vapor atomic absorption spectrometry (CVAAS) to determine the ions in the chosen food samples.

Preparation of dopamine/L-cysteine modified PVDF composite membrane and its application in the removal of mercury ions from water

Polyvinylidene fluoride (PVDF), embodying a stabilization under thermal environment and capability to resist chemical corrosion, is widely used as a membrane-forming material. However, its inherent hydrophobicity and lack of active functional groups in the structure limit its suitability for adsorption applications. In this study, PVDF-based membranes were first prepared by the non-solvent phase inversion method, and then, polydopamine (PDA) was coated on these membranes by the oxidative self-polymerization of dopamine (DA). Then, L-cysteine (LCys) was grafted by self-assembly to obtain a highly hydrophilic PVDF composite (PVDF@PDA-LCys) membrane with excellent ability for Hg(II) ion capture. The membrane has the following characteristics: excellent hydrophilicity, with a water contact angle (WCA) that drops to 0° within 3s, which is far superior to the 89.22° WCA of the PVDF-based membrane. Given an 10mg·L-1 initial concentration of Hg(II), adsorption experiences 120min, the removal efficiency reaches 95.14%. The fitted maximum adsorption capacity is 97.98mg·g-1. Additionally, the composite membrane exhibits good acid resistance. When the solution pH is as low as 1.5, the Hg(II) ion removal efficiency is still close to 70%. The performance of the composite membrane remains stable after repeated use. This study demonstrates an environmentally friendly and practical method for preparing PVDF-based composite membranes with potential applications in wastewater treatment.

Probing the potential of mercury removal by covalently immobilized phycobiliproteins onto the surface of chitosan beads

Mercury emissions represent a significant risk to the environment and human health. Mercury is persistent and can circulate in the environment for thousands of years, which is why treating this toxic metal is important. Chitosan polymer is easily obtainable, and it has good mercury adsorption characteristics. This study aimed to improve its capabilities to absorb mercury by immobilizing phycobiliproteins (PBPs) onto the surface of chitosan beads (chitosan–PBPs). Phycobiliproteins, light-harvesting proteins from algae and cyanobacteria, have several industrially essential applications. These proteins can bind heavy metals with high affinities. Protein extracts obtained from both Arthrospira platensis, with C-phycocyanin (C-PC) as the primary protein, and Porphyra yezoensis, with R-phycocyanin (R-PC) and R-phycoerythrin (R-PE) as the dominant PBPs, were covalently immobilized onto chitosan beads. Beads with immobilized PBPs were characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. Binding analysis showed that, on average, each chitosan bead weighed 20 mg and immobilized 63.54 μg of PBPs from Spirulina and 44.12 μg of PBPs from Porphyra. Immobilized proteins were still in their native state, with no visible color change months after immobilization. Chitosan–PBPs and chitosan alone were tested for mercury adsorption at pH 4 and pH 7 by atomic absorption spectroscopy. The tested concentration range of mercury was from 1 to 70 ppm. Affinity, calculated using Henry's binding isotherm, of chitosan–PBPs for mercury was twice as much higher at both pH values than chitosan alone. Furthermore, chitosan-PBP beads were able to absorb more mercury than chitosan alone. These results showed that the covalent immobilization of PBPs onto chitosan improves its mercury adsorption characteristics and creates a more efficient eco-friendly adsorbent to potentially remove mercury ions in the tested concentration range from polluted waters.

A carboethoxy quinoline-Derived Schiff base chemosensor: Crystal structure, selective Hg2+ ion detection and its computational study

Environmental monitoring of mercury (Hg2+) ions has become increasingly important as a result of their detrimental effects on biological organisms at all levels. To recognize toxic metal ions, utmost effort has been devoted to developing new materials that are highly selective, ultra-sensitive, and provide rapid response. In this context, a new chemosensor, 2-imino [N - (N-amido phenyl)]-6-methoxy-3-carbethoxy quinoline (L), has been synthesized by combining 2-formyl-6-methoxy-3-carbethoxy quinoline and benzhydrazide and it has been extensively characterized by NMR, FTIR, ESI-Mass and SCXRD analysis. Probe L has excellent specificity and sensitivity toward Hg2+ ions in semi-aqueous solutions, with a detection limit of 0.185 μM, regardless of the presence of other interfering cations. Chromogenic behavior was demonstrated by the L when it changed the color of the solution from colorless to light yellow, a change that can be observed visually. The probe L forms a 1:1 stochiometric complex with an estimated association constant (Ka) of 6.74 × 104 M−1. The 1H NMR change and density functional theory calculations were analyzed to improve our understanding of the sensing mechanism. Also, an inexpensive and simple paper-based test kit has been developed for the on-site detection of mercury ions in water samples.

Development and sensitivity analysis of MWCNTs coated D-shaped plastic optical fiber sensor for the detection of mercury

Heavy metal pollutants in rivers and water catchments are one of the problems faced by many developing countries as they may result in health issues among their people. A proper sensing mechanism is required to ensure the quality of water. In this research, we propose a simple, low cost, and highly sensitive D-shaped plastic optical fiber (POF) sensor layered with functionalized multi-walled carbon nanotubes (MWCNTs) for the detection of mercury in water. The sensor underwent interrogation across a range of mercury concentrations at room temperature. Numerous methods of characterization have been employed to explore the intricate structural attributes of the sensing layer to verify that the nanocomposite surface layer is functionalized with minimal disruption to the nanotubes. The experimental results revealed that the coated sensor displayed swift response and recovery time of 6.3 s and 13 s respectively when tested with the dynamic mercury concentration range (0 to 5 ppm). Moreover, it exhibited a relative absorbance of 7.33 %/ppm, which is approximately four times higher than the plain sensor and a limit of detection (LOD) of 0.1 ppm. The sensor has the potential to be transformed into an on-site, portable, real-time optical sensor for the detection of mercury ions in drinking water, offering high sensitivity and fast data acquisition.

Revealing the Interaction Forms between Hg(II) and Group Types (–Cl, –CN, –NH2, –OH, –COOH) in Functionalized Poly(pyrrole methane)s for Efficient Mercury Removal

To explore the impact of different functional groups on Hg(II) adsorption, a range of poly(pyrrole methane)s functionalized by –Cl, –CN, –NH2, –OH and –COOH were synthesized and applied to reveal the interaction between different functional groups and mercury ions in water, and the adsorption mechanism was revealed through combined FT-IR, XPS, and DFT calculations. The adsorption performance can be improved to varying degrees by the incorporation of functional groups. Among them, the oxygen-containing functional groups (–OH and –COOH) exhibit stronger affinity for Hg(II) and can increase the adsorption capacity from 180 mg·g-1 to more than 1400 mg·g-1 at 318 K, with distribution coefficient (Kd) exceeding 105 mL·g-1. The variations in the capture and immobilization capabilities of functionalized poly(pyrrole methane)s predominantly stem from the unique interactions between their functional groups and mercury ions. In particular, oxygen-containing –OH and –COOH effectively capture Hg(OH)2 through hydrogen bonding, and further deprotonate to form the –O–Hg–OH and –COO–Hg–OH complexes which are more stable than those obtained from other functionalized groups. Finally, the ecological safety has been fully demonstrated through bactericidal and bacteriostatic experiments to prove the functionalized poly(pyrrole methane)s can be as an environmentally friendly adsorbent for purifying contaminated water.

A novel 1,3-diazepine-based fluorescent probe for highly selective detection of Hg2+

A novel 1,3-diazepine based fluorescent probe for Hg2+ has been successfully synthesized and characterized. Comprising a furan and pyridine, the probe L1 is a blue-emitting 1,3-diazepine derivative, which transforms into an imine form with high fluorescent yellow-emitting under alkaline conditions. Fluorescence quench of the probe in ethanol was observed with the addition of Hg2+ aqueous in the presence and absence of other metal ions, with a visible color change from colorless to yellow, and this fluorescence quench can be observed in a wide pH range of 3–11. An important feature for this probe is its high selectivity towards mercury ions for the aqueous-phase detection of Hg2+ over the other competitive metal ions, making the “naked-eye” detection of mercury ions possible.

Toxicity of vapor-gas flows from technogenic substance

The relevance. Vapor-gas flows from technogenic substances (storage wastes of the mining industry), carrying a high amount of potentially toxic elements, are a big problem for the environment and the population, because metals and metalloids in the composition of emanations are in an easily digestible bioavailable forms and are able to easily penetrate into living organisms. The main aim of this study is an assessment of toxicity for living organisms of air mixtures containing gaseous products emitted by a surfaces of mine tailings freely located near settlements and under the influence of climatic factors and microorganisms. Methods. Carrying out experiments with white rats male Wistar, analysis of organs for the content of a wide range of elements by ICP-MS on a NexION 300D mass spectrometer (PerkinElmer, USA) (PNL  GGC IShPR TPU). In the experiment, a pooled sample of the waste substance was used. The sample was analyzed for the content of oxides of the silicate group by XRF using X-ray fluorescence spectrometer ARL-9900-XP (Thermo Electron Corporation, Switzerland) at the Laboratory of X-ray Spectral Analysis Methods of the IGM SB RAS; elemental analysis was carried out by ICP-MS using an ELAN-9000 DRC-e instrument Perkin Elmer, USA (HAC Plasma). Results. Under the influence of vapor-gas emanations from the substance of arsenide tailings of the Tuvacobalt plant on a group of rats male Wistar, pathological changes occurred in the experimental group. Small foci of hemorrhages formed in the lungs, the tissues became edematous and inflamed. The liver of all animals increased, the share structure became sharply expressed, the color became light beige. Single hemorrhages were found in the kidneys. The vessels of the meninges are dilated, petechial hemorrhages are observed. The synthetic function of cells and the stability of cellular and intracellular membranes were disrupted, first of all, the endothelium of blood vessels was affected, the physiological functioning of organs and tissues was disrupted with the accumulation of intermediate products of biochemical reactions, determined macroscopically. Also, dystrophy of internal organs was determined, in particular, the liver, lungs, kidneys, and brain. Elemental analysis of animal organs showed the accumulation of toxic elements in comparison with the control group. The most characteristic elements, the excess of which was recorded in most cases, are mercury and arsenic. They were unevenly distributed throughout the organs. Mercury accumulated mainly in the lungs, kidneys and liver, while arsenic accumulated mainly in the liver and brain. This may indicate the entry of mercury and arsenic ions in a biologically available form into the bloodstream by inhalation, and local irritating and toxic effects on the lungs were not prevailing, and the liver was the most damaged organ according to the results of toxicochemical and morphological studies. The homeostasis of micro and macro elements is finely regulated, and any concentration imbalance in the form of a deficiency leads to a progressive decrease and disruption of normal biological function, to severe physiological and clinical outcomes, which we observed from the results of the experiment. The data obtained proved the acute toxic effect of vapor-gas flows on living organisms, and also confirmed the possibility of the removal of many chemical elements in easily accessible and assimilable forms.

Coumarin derivative-functionalized nanoporous silica as an on–off fluorescent sensor for detecting Fe3+ and Hg2+ ions: a circuit logic gate

A highly efficient fluorescent sensor (S-DAC) was easily created by functionalizing the SBA-15 surface with N-(2-Aminoethyl)-3-Aminopropyltrimethoxysilane followed by the covalent attachment of 7-diethylamino 3-acetyl coumarin (DAC). This chemosensor (S-DAC) demonstrates selective and sensitive recognition of Fe3+ and Hg2+ in water-based solutions, with detection limits of 0.28 × 10–9 M and 0.2 × 10–9 M for Hg2+ and Fe3+, respectively. The sensor’s fluorescence characteristics were examined in the presence of various metal ions, revealing a decrease in fluorescence intensity upon adding Fe3+ or Hg2+ ions at an emission wavelength of 400 nm. This sensor was also able to detect ferric and mercury ions in spinach and tuna fish. The quenching mechanism of S-DAC was investigated using UV–vis spectroscopy, which confirmed a static-type mechanism for fluorescence quenching. Moreovre, the decrease in fluorescence intensity caused by mercury and ferric ions can be reversed using trisodium citrate dihydrate and EDTA as masking agents, respectively. As a result, a circuit logic gate was designed using Hg2+, Fe3+, trisodium citrate dihydrate, and EDTA as inputs and the quenched fluorescence emission as the output.Graphic abstract

Environmentally friendly use of silver nanoparticles prepared with Anchusa azurea flower to detect mercury (II) ions

ABSTRACT In this study, the extract obtained from the flowers of the Anchusa azurea (AA) plant was mixed with silver nitrate to obtain silver nanoparticles. The ion sensing ability of the obtained bio-sourced silver nanoparticles in aqueous solutions was investigated and the presence of Hg2+ ions was determined colorimetrically. Silver nanoparticles (AgNPs) prepared on Green Chemistry method, which is both an environmentally friendly and cost-effective synthesis technique, were characterised using different analytical tools. The mean particle size of AA-AgNPs from transmission electron microscopy (TEM) images was determined to be 22 nm in diameter. XRD measurements showed that the crystallite sizes of the synthesised AgNPs were in the face-centred cubic crystal structure with an average size of 22 nm, which is consistent with TEM results. AA-AgNPs showed absorption at 435 nm, indicating that AgNPs exhibit a strong surface plasmon resonance (SPR) and play a role in stabilisation. AgNPs synthesised with Anchusa azurea flowers were observed using UV-vis spectroscopy to selectively and sensitively detect mercury ions (Hg2+). When Hg2+ in aqueous solution was added to the AgNPs, the overall absorbance dramatically decreased and the colour changed from yellow to colourless. This study shows that AA-AgNPs can be used as a cost-effective material in optical sensors for colorimetric determinations.

Coumarin Derivative and Gold Nanoparticle Conjugate as a Selective Fluorescent Sensor for Mercury Ion in Real Sample.

A biphenyl based coumarin fluorescent molecule, N,N'-bis(7-diethylamino-2-oxo-2H-chromen-3-yl)methylene)biphenyl-2-2'-dicarbohydrazide (molecule 1) has been synthesized and characterised. Photophysical studies of 1 exhibit solvent polarity dependent absorption and emission maxima. Citrate capped gold nanoparticles (AuNPs) have been mixed with molecule 1 for the preparation of AuNPs/1 conjugate. The association constant of the AuNPs/1 conjugate has been calculated to 4.54 × 104 M- 1. The AuNPs/1 conjugate has been found to detect Hg2+ ion selectively by fluorescence enhancement. While addition of molecule 1 into the solution of AuNPs, fluorescence intensity of 1 quenched. On addition of several monovalent, divalent and trivalent metal ion into the solution of AuNPs/1 conjugate separately, there was no change in fluorescence intensity of 1 has been observed. However, upon addition of Hg2+ ion into the solution of AuNPs/1 conjugate, the fluorescence intensity enhancement occurred, indicating released of 1 from the surface of AuNPs and probably aggregation of AuNPs took place in presence of Hg2+ ion. The AuNPs/1 conjugate has been found to have a detection limit of 2.3 × 10- 9 M for Hg2+ ion in aqueous solvent. Meanwhile, the AuNPs/1 conjugate have also been successfully applied for the determination of Hg2+ in real water samples.

Portable analysis of tract mercury ions by a hydrogel-based ratiometric fluorescence sensor using C3N4-CdTe0.16S0.84 QDs nanocomposites

The portable detection of trace mercury ions (Hg2+) in water is crucial for preventing and controlling mercury pollution. In this study, graphitic carbon nitride nanoparticles (CNNPs) with green fluorescence as the self-calibration signal were synthesized by a one-pot solvothermal method. Cadmium telluride sulfide quantum dots (CdTe0.16S0.84 QDs) with red fluorescence as a response signal were prepared using an oxidation-reduction method. Thus, a new ratiometric fluorescence sensor based on CNNPs-CdTe0.16S0.84 QDs was constructed for the visual detection of trace Hg2+. The linear range of the sensor was from 0.05 to 2525 nM, with a detection limit of 0.009 nM. The sensor displayed higher sensitivity to Hg2+ compared to copper ions and silver ions. The fluorescence quenching behavior and the source of sensitivity for the three metal ions were investigated using the Stern-Volmer equation and density functional theory. The results suggest that the high sensitivity to Hg2+ may arise from electron transfer and electrostatic interactions between Hg2+ and CdTe0.16S0.84 QDs. Building on this proposed strategy, a new smartphone-assisted CNNPs-CdTe0.16S0.84 QDs hydrogel-based fluorescence sensor was constructed for portable on-site analysis of trace Hg2+. This new method will facilitate the on-site monitoring of hazardous substances in environmental water.