Detection Of Mercury Research Articles

AuNPs enhanced electrochemical and optical dual-mode fiber optic sensor for trace Hg2+ detection

Efficient and low-concentration detection of heavy metal ions is crucial for healthcare and environmental monitoring. Traditional fiber optic surface plasmon resonance (SPR) sensors face challenges in detecting trace heavy metal ions due to limited sensitivity and the need for complex specific modifications. To overcome these challenges, an innovative electrochemical and optical dual-mode fiber optic sensor for in situ, real-time detection of trace mercury ions is proposed in this paper. The sensor utilizes a reflection-type fiber optic probe coated with thin gold (Au)/indium tin oxide (ITO) film and gold nanoparticles (AuNPs), enabling simultaneous electrochemical and optical interrogation. The coupling effect between the SPR of thin film and the localized surface plasmon resonance (LSPR) of AuNPs significantly improves optical sensitivity, with AuNPs also offering additional active sites for the redox reaction of Hg2+. The ITO film not only facilitates the stripping of Hg2+, leading to sharper stripping peaks but also enhances the ability of the sensor to rapidly respond to anomalous potential changes. Experimental results show that the sensor has a wide dynamic detection range from 10−10 M to 10−5 M, with a limit of detection reaching the pM level. The dual-mode functionality allows the simultaneous collection of voltage, current, and optical information, enabling cross-validation of the detection results and improving the accuracy and reliability of detection.

Tripartite Detection and Sensing of Toxic Heavy Metals Using a Copper-Based Porphyrin Metal-Organic Framework.

The detection of heavy metals in water sources is a critical concern for environmental preservation and public health. However, current electrochemical heavy metal sensors suffer from high sensing limits, cross-sensitivity, and poor selectivity. In this work, we present the possibility of an electrochemical sensor based on a copper (Cu) metal-organic framework for the detection of lead, cadmium, and mercury by replacing Cu metal nodes. The working electrode consists of a ∼5 μm thin layer of copper- tetracarboxyphenylporphyrin (Cu-TCPP) sheets that are adsorbed on a glassy carbon electrode (GCE). Upon interaction with Pb2+, Cd2+, and Hg2+, these ions are adsorbed on and incorporated into the metal nodes of the MOF. The adsorbed metallic species can be oxidized to the ionic form (Pb → Pb2+) electrochemically, which results in an oxidation response and enables the quantitative detection of these metals. The oxidation peak currents follow a (mostly) bimodal linear regression with a sensing range of up to 30 μM dependent on the deposition time and an ultralow limit of detection (LoD) of up to 5 nM. The system displays robust and selective sensing in saturated solutions of counterions and interfering metal ions (low error margins of <10%). This work represents the first report of a Cu-TCPP-modified GCE anode as an effective electrode for the sensitive detection of multiple heavy metals and an in-depth study into the Cu replacement kinetics of the Cu-MOF.

Tailoring polythiophene nanocomposites with MnS/CoS nanoparticles for enhanced SERS detection of mercury ions in water

The excessive emission of heavy metal ions from industrial processes poses a serious threat to both the environment and human health. This study presents a novel approach using PTh-MnS/CoS NPs for the selective and sensitive detection of Hg2+ ions in water. Such detection is crucial for safeguarding human health, protecting the environment, and assessing toxicity. The fabrication method employs a simple and efficient chemical precipitation technique, combining polythiophene, MnS, and CoS NPs to create active substrates for SERS. The MnS@Hg2+ exhibits a distinct Raman shift at 938 cm−1, enabling specific identification and showing the highest responsiveness among the studied semiconductor substrates with a detection limit of only 1 nM. This investigation shows reliable and practical SERS detection for mercury ions. The RSD ranged from 0.49 % to 9.8 %, and recovery rates varied from 96 % to 102 %, showing selective adsorption of Hg2+ ions on the synthesized substrate.

Engineering a Graphene Quantum Dot‐Enhanced Surface Plasmon Resonance Sensor for Ultra‐Sensitive Detection of Hg2⁺ Ions

AbstractThe contamination of soil and water by heavy metals poses a significant environmental and public health concern worldwide. To address this issue, a novel graphene quantum dot (GQD)‐based surface plasmon resonance (SPR) sensor is developed for the detection of mercury ions (Hg2+), a notorious heavy metal pollutant. The thiol and amine‐functionalized GQDs (S,N‐GQDs), synthesized via pyrolysis of citric acid and L‐cysteine, are directly immobilized onto the SPR chip surface without prior pretreatment, demonstrating their potential as efficient sensing materials. The SPR sensor exhibits high sensitivity and selectivity toward Hg2+ ions, as confirmed by kinetic binding analysis and isotherm modeling. The Langmuir isotherm model, which accurately describes the interactions between Hg2+ and S,N‐GQDs, provides insights into the sensor's mechanism of action. Furthermore, the sensor demonstrates robustness and reusability, with recoveries ranging from 98% to 104% over multiple cycles of analysis. Given the presence of contaminants in tap water, the developed sensor system holds significant importance for environmental monitoring and public health protection, offering a rapid, accurate, and cost‐effective solution for detecting Hg2+ ions in such samples. Overall, this study represents a significant advancement in the field of heavy metal detection, with potential implications for addressing environmental pollution and ensuring water quality.

Detection of Silver and Mercury Ions Using Naphthalimide-Based Fluorescent Probe.

A multifunctional fluorescent probe P based on a naphthalimide derivative for the detection of Ag+ and Hg2+ through a dual-signal was designed and characterized. P exhibited a large Stokes shift (107 nm), high selectivity, good sensitivity, and fast response time. By adjusting the testing medium and the order of reagent addition, multifunctional detection with P was achieved. The addition of Ag+ or Hg2+ to P solution in either ethanol or an ethanol-water mixture resulted in a significant quenching of fluorescence emission at 537 nm and caused a decrease in the absorbance at 440 nm accompanied by the appearance of a new absorption peak at around 340 nm, and there was an obvious color change from yellow to colorless. In contrast, the addition of other common metal ions and anions did not produce substantial spectral or color changes. The detection limit of probe P for Ag+ and Hg2+ was calculated to be 0.33 μM. The sensing mechanism was proposed and validated through MS and 1H NMR spectrometry methods. Additionally, P demonstrated the capability to recognize Ag+ and Hg2+ in living cells with satisfactory results.

A rapid colorimetric sensor for the detection of mercury in environmental samples employing 2 aminobenzohydrazide schiff base functionalized silver nanoparticles

Mercury (Hg2+) is an extremely toxic and dangerous element for living organisms. Herein, a simple and selective sensor based on the Schiff base of 2-aminobenzohydrazide with triazole thiazole substituted vanillin (EAHT) functionalized silver nanoparticles (EAHT-AgNPs) is proposed for the detection of Hg2+ in environmental water samples. The chemical reduction method was employed to synthesize EAHT-AgNPs using sodium borohydride as the reducing agent. The synthesized nanoparticles were initially confirmed by UV-visible and FTIR spectroscopy, followed by analysis with a zeta sizer to determine their average size, surface charge and polydispersity index. The atomic force microscopy (AFM) and scanning electron microscopy (SEM) were employed to determine the size and morphology of EAHT-AgNPs. Additionally, the functionalized particles exhibited stability at varying pH values, salinity concentrations and elevated temperature. The addition of Hg2+ altered the yellow color of EAHT-AgNPs to colorless, confirming the complex formation. The analytical response constructed as a decrease in absorbance versus concentration showed linearity (R2 = 0. 991) from 0.1 to 100 µM with a limit of detection of 0.04 µM (40 nM) and limit of quantification of 0.085 µM (85 nM). The sensor was successfully applied for the detection of Hg2+ ions in tap water. In conclusion, Schiff base of 2-aminobenzohydrozide with triazole thiazole substituted vanillin silver nanoparticle-based chemosensor is highly sensitive and selective for the detection of Hg2+ in water samples. The proposed sensor has been applied for mercury detection tap water, future research should explore its applications in more complex samples like industrial wastewater and marine environments. Further, studies may focus on the integrating of the approach into the portable devices such as smartphone for on-site detection of mercury.

Peptide-Based Rapid and Selective Detection of Mercury in Aqueous Samples with Micro-Volume Glass Capillary Fluorometer

Mercury, a toxic heavy metal produced through both natural and anthropogenic processes, is found in all of Earth’s major systems. Mercury’s bioaccumulation characteristics in the human body have a significant impact on the liver, kidneys, brain, and muscles. In order to detect Hg2+ ions, a highly sensitive and specific fluorescent biosensor has been developed using a novel, modified seven amino acid peptide, FY7. The tyrosine ring in the FY7 peptide sequence forms a 2:1 complex with Hg2+ ions that are present in the water-based sample. As a result, the peptide’s fluorescence emission decreases with higher concentrations of Hg2+. The FY7 peptide’s performance was tested in the presence of Hg2+ ions and other metal ions, revealing its sensitivity and stability despite high concentrations. Conformational changes to the FY7 structure were confirmed by FTIR studies. Simultaneously, we designed a miniaturized setup to support an in-house-developed micro-volume capillary container for volume fluorometry measurements. We compared and verified the results from the micro-volume system with those from the commercial setup. The micro-volume capillary system accommodated only 2.9 µL of sample volume, allowing for rapid, sensitive, and selective detection of toxic mercury (II) ions as low as 0.02 µM.

Colorimetric Detection and Automatic Quantitative Analysis of Mercury(II) Ions via Selective Redox Reaction Sites on Silver-Coated Gold Nanorods

Colorimetric Detection and Automatic Quantitative Analysis of Mercury(II) Ions via Selective Redox Reaction Sites on Silver-Coated Gold Nanorods

An electrochemical biosensor for mercury(II) detection based on DNA-Au bio-bar codes coupled with enzymatic dual signal amplification

An electrochemical biosensor for mercury(II) detection based on DNA-Au bio-bar codes coupled with enzymatic dual signal amplification

Design and demonstration of a temperature-resistant aptamer structure for highly sensitive mercury ion detection with BioFETs

In this study, we developed a temperature-resistant aptamer coupled with extended gate electric double-layer Field-Effect Transistors (FETs) for highly sensitive mercury ion detection. The design of the temperature-resistant aptamer is based on the thermal and structural properties of the hairpin structure. Two aptamer sequences were designed with different melting temperatures (Tm) and compared for their sensitivity. The hairpin structure of the aptamer with a high melting temperature ensures the stable structure prior to the addition of the mercury ions, which allows the formation of thymine–mercury–thymine (T -Hg2+-T) complex in low concentrations of mercury ions. High sensitivity and low detection limit are achieved at elevated temperatures with the aptamer having a high melting temperature. The elevated temperature facilitates the reaction rate, resulting in high sensitivity and a low detection limit. The aptamer with a high melting temperature hairpin structure has shown a remarkable improvement in the limit of detection with a 4 orders of magnitude increase compared to the one with a low melting temperature. The sensor with the high melting temperature aptamer shows an extremely low detection limit of 4.68 × 10−12 M, surpassing previously reported results. The aptamer with a low melting temperature requires mercury ions to stabilize the hairpin structure by forming a T-Hg2+-T complex. The results show that if the melting temperature is lower than the ambient temperature, it is very difficult to detect low concentrations of mercury ions at the ambient temperature. The selectivity of this sequence was also tested against multiple heavy metals, including arsenic (As), lead (Pb), chromium (Cr), and cadmium (Cd) ions. This study has shown how the structural and thermal properties of the aptamer, and the ambient temperature affect the sensitivity. They are strongly correlated to the performance of the sensors and need to be considered in the design of the sequence.

Converting Plastic Waste into Functional Carbon Nanodots for the Selective Detection of Iron and Mercury Ions

Converting Plastic Waste into Functional Carbon Nanodots for the Selective Detection of Iron and Mercury Ions

A RAPIDLY COLORIMETRIC DETECTION OF ARSENIC AND MERCURY IONS BASED ON SURFACE PLASMON RESONANCE ABSORBANCES OF FUNCTIONALIZED AuNPs IN COSMETICS

In this study, a novel colorimetric method is developed for the detection of arsenic and mercury ions, utilizing the surface plasmon resonance (SPR) properties of AuNPs ([Formula: see text] nanoparticles) functionalized with APT ([Formula: see text]-(3-aminophenyl) tetrazole). Theoretical calculations confirm the findings from UV–Visible spectroscopy and transmission electron microscopy analyses, indicating that APT is electrostatically bound to the surfaces of the AuNPs. The introduction of [Formula: see text] and [Formula: see text] ions triggers a coordination reaction with APT, resulting in a reduced interparticle distance among the AuNPs. This change leads to a visible color shift of the solution from wine red to bluish-gray. The detection limits for [Formula: see text] and [Formula: see text] are determined to be 0.6 and 0.24 [Formula: see text] g⋅[Formula: see text], respectively, distinguishable to the naked eye. A robust linear correlation is observed between the absorbance ratios and the ion concentrations, with correlation coefficients ([Formula: see text]) of 0.990 for [Formula: see text] and 0.998 for [Formula: see text]. These findings demonstrate that AuNPs functionalized with APT are effective for the quantitative analysis of arsenic and mercury ions. The sensor exhibits high selectivity and excellent resistance to interference, indicating its potential applicability for monitoring [Formula: see text] and [Formula: see text] in tap water and cosmetic products.

Preparation and application of a new ion-imprinted polymer for nanomolar detection of mercury(II) in environmental waters

This study introduces a novel ion-imprinted polymer for the ultrasensitive detection of mercury(II) in water. The ion-imprinted polymer was synthesized via a simple bulk polymerization process using methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as the cross-linker, morpholine-4-carbodithioic acid phenyl ester as the chelating agent, and ammonium persulfate as the initiator. The electrochemical mercury(II) sensing capability of the ion-imprinted polymer was studied via the modification of a cost-effective carbon paste electrode. A stripping voltammetric technique was utilized to quantify the analyte ions following open-circuit enrichment. Critical experimental parameters, including the nature and concentration of the eluent, solution pH, preconcentration duration, ion-imprinted polymer dosage, sample solution volume and reduction potential, were systematically studied and optimized. Under optimal conditions, the sensor exhibited a linear response in the range of 1.0 to 240.0 nM, with a low detection limit of 0.2 nM. The sensor demonstrated remarkable selectivity against potential interfering ions, including lead(II), cadmium(II), copper(II), zinc(II), manganese(II), iron(II), magnesium(II), calcium(II), sodium(I) and cobalt(II). The practical applicability of the developed method was successfully validated through the analysis of real water samples, suggesting its potential for environmental monitoring applications.

Solid-Phase Microextraction Mediated Solid-Phase Dielectric Barrier Discharge Vapor Generation-Atomic Fluorescence Spectrometry for Sensitive Determination of Mercury in Seawater.

A novel method coupling solid-phase microextraction (SPME) to solid-phase dielectric barrier discharge (SPDBD) vapor generation was proposed and used for the sensitive detection of trace mercury (Hg) in seawater with atomic fluorescence spectrometry (AFS) in this work. The method proposed herein offers the unique advantages of integrating desorption and chemical vapor generation into one step, eliminating the use of elution reagents, and reducing the analysis time. SPME with multiwalled carbon nanotubes (MWCNTs) coated on the glass tube was used to extract Hg2+ in seawater. The Hg2+ was then desorbed and reduced to Hg0 vapor by SPDBD, which was detected by cold vapor AFS. The parameters affecting Hg2+ extraction, desorption, and vapor generation were studied. The detection limit of Hg2+ was 0.0003 μg L-1, and the relative standard deviation at a Hg2+ concentration of 0.05 μg L-1 was 4.4%. This method also has excellent antimatrix interference ability for Hg2+ determination with recoveries between 91.8% and 101.1% in the presence of extremely high concentrations (two million times excess) of coexisting ions. The practicality of this method was also evaluated by analyzing two different certified reference materials of Hg2+ in water and several seawater samples with good spike recoveries (94.0%-107.4%). Compared with solid-phase photothermo-induced vapor generation, this method has higher extraction efficiency and higher desorption efficiency without the assistance of heating as well as a lower detection limit of Hg2+, which is capable of performing trace Hg analysis in seawater.

Reactive Fluorescent and Colorimetric Probe for Highly Selective and Sensitive Detection of Hg2+ in Real Water Samples.

Construction of efficient chemosensors for highly specific and sensitive detection of mercury ions remains a great challenge. In this work a highly selective and sensitive probe CY was designed and synthesized by using coumarin fluorophore as the matrix and thioacetal moiety as the reactive recognition site for Hg2+. By virtue of the thiophilicity of Hg2+, probe CL could be hydrolyzed to deprotect and the thioacetal was transformed to the acyl group after the addition of Hg2+, the blue-green fluorescence was quenched and meanwhile the solution changed from light green to yellow. The detection limit of probe CY for Hg2+ was as low as 6.8 nM, and it could completely react with Hg2+ within 3min. Moreover, probe CY exhibited good resistance against interference from competitive metal ions and biothiols, high stability in pH 1-11 and applicability for fluorogenic and chromogenic dual-modal detection of Hg2+ in real water samples over a broad range of pH 5-10.

1D supramolecular assembly-induced emission and colorimetry toward precise onsite mercury(II) detection

Manipulation of the one-dimensional (1D) supramolecular assembly of platinum(II) terpyridyl complex is promising for achieving precise onsite mercury(II) detection in complex environments, but still challenging. Herein, by systematic molecular design of platinum(II) terpyridyl complex, chloride-mediated 1D supramolecular assembly has been successfully achieved, exhibiting not only improved recognition ability but also dual-visual signal, with turn-on red luminescence and high-contrast color change from pale-yellow to orange-red. The probe also shows excellent selectivity and anti-interference properties, fast response rate (< 1 s) and low detection limit, stretching to 20.6 fg when incorporated in a hydrogel matrix. Structure insight for the dual-visual response shows that this high detection performance derives from the ancillary ligand of -NCS, which endows the increase of ion-association ability between platinum(II) terpyridyl complex and [HgCl4]2−, leading that 1D packing mode with strengthened Pt-Pt interactions. In all, this work highlights a new strategy of 1D supramolecular assembly construction for high performance detection of heavy metal ions.

Synthesis, characterization, and application of novel fluorescent sporopollenin for effective detection of mercury (II) ions from aqueous media

In this investigation, a novel environmentally friendly functionalized fluorescent Sp-TAB hybrid material was advanced for the sensitive detection of environmentally polluting Hg(II). The characterization of the synthesized fluorescent Sp-TAB hybrid material using SEM and EDX provided insights into morphological and structural changes in the material's pore structure, while XRD and FT-IR analyses revealed the impact of the prepared material at each stage. Optimal parameters such as temperature, contact time, and pH influencing Hg(II) ion detection were determined. Application of the fluorescent Sp-TAB hybrid material was determined a detection limit (LOD) of 4.87 μM for Hg(II) ions. This study shows the potential of the immobilization-enhanced fluorescent Sp-TAB hybrid material for sensitive Hg(II) ion detection in tap water. Additionally, this study is believed to serve as a model for sensitive and practical detection applications of heavy metals in the future.

Mercury Detection in Novel Foods by a Smart Pocket Sensor

AbstractMercury is one of the most well‐known toxic contaminants of natural and anthropogenic origin in aquatic ecosystems that can bioaccumulate in vegetal and animal organisms. In this work, we propose a smart detection system for Hg(II) ions by square wave anodic stripping voltammetry at nanocomposite graphite screen‐printed electrodes, as an analytical tool to be applied in food quality control. The nanocomposite surfaces were obtained by the modification of screen‐printed graphite electrodes with poly(l‐aspartic acid) and gold nanoparticles and were characterized by means of electrochemical techniques. An exhaustive study of the experimental conditions involved both in the electropolymerization and in the voltammetric stripping measurements was addressed to develop a reliable method capable of measuring Hg(II) concentration in the low μg/L range, both in conventional and drop configurations. The sensor was integrated in a smart setup, comprising a Sensit Smart pocket instrument connected to a smartphone, thus proving its applicability for in situ analysis due to its cost‐effectiveness. The analytical significance of the developed sensor was assessed by detecting Hg(II) in novel food samples.

Rational Design of Regenerable Amino-Functionalized Fluorescent Covalent Organic Framework for the Exclusive Detection of Mercury(II).

Goal-oriented development of novel covalent organic frameworks (COFs) to construct a sensing platform for highly toxic mercury (II, Hg2+) is of tremendous significance. Recently, numerous COFs with sulfur-based ligands were developed for Hg2+ monitoring; however, strong binding of Hg2+ by sulfur makes their regeneration very tough. Herein, we designed and developed an amino-functionalized fluorescent COF (COF-NH2) through facile postmodification for Hg2+ detection in which the π-conjugation skeleton is the signal reader and the nitrogen-based side is the highly selective Hg2+ receptor. More importantly, this nitrogen-based receptor permits the reversible binding of Hg2+. As a sensing platform, the outstanding performance of COF-NH2 for Hg2+ detection was reached with respect to high sensitivity with an ultralow detection of 15.3 nM, real-time response with rapid signal change of 10 s, and facile visualization with significant fluorescence color change. Expectedly, COF-NH2 obtained facile recycling which still shows excellent response performance toward Hg2+ after six cycles based on the reversible interaction between amino groups and Hg2+. Our work not only shows an attractive foreground of fluorescent COF for Hg2+ detection but also emphasizes the easy construction of novel COF materials via the rational introduction of metal ligands for the recognition of other metal ions.

Utilization of Schiff base ligands to chelate Ag+ for highly specific and sensitive Hg2+/Ag+ immunoassay

In this study, a planar benzothiazole Schiff base derivative ZX1 was designed and synthesized to selectively precipitate silver ions, in conjunction with the immunoassay detection of Hg2+ ions. The silver chelation process was highly effective in the pH range of 7–10, with a silver ion precipitation ratio of 99.9 %. The coordination behavior of ZX1 with Ag+ was studied using a series of spectroscopic measurements, topography analysis and DFT calculation. The shortest bond distances were 2.251 and 2.254 Å between nitrogen atom of thiazole and Ag+. Weak interactions were analyzed using the interaction region indicator (IRI) method and VMD. The immunoassay was developed through an anti-Hg2+/Ag+ monoclonal antibody, which showed similar sensitivities for Ag+ and Hg2+. The selectivity and anti-interference ability of the Schiff base ligands were tested for some hard metal ions and several anions. With co-existence of interference ion Ag+, Hg2+ was detected in rice matrix solution with 77 %∼123.5 % recovery by addition of ZX1 as the masking reagent and 90.3 %∼115 % for wheat matrix. This research provides a promising immunoassay strategy for simultaneous detection of silver ions and mercury ions in food matrix by utilization of Schiff base ligands. This novel Schiff base ligand was then used as the pre-treatment reagent to remove silver ions within 5 min for detection of Hg2+ or detection of both Ag+ and Hg2+ based on a novel bi-specific heavy metal antibody.