Determination Of Trace Amounts Research Articles

An efficient microchip electromembrane extraction online with high-performance liquid chromatography for the measurement of nicotine in high consumption vegetables.

Nicotine, a highly addictive substance, is naturally produced in the Solanaceae family of plants, particularly tobacco. The presence of nicotine in plant foods has adverse effects on the lungs, kidneys, heart, and reproductive system. A novel three-phase microchip flat electromembrane coupled with online high-performance liquid chromatography (HPLC) was developed to analyze nicotine in tomato, mushroom, eggplant, bell pepper, and red pepper. The microchip was connected to the HPLC in online mode. All effective variables were optimized to achieve the best extraction response. The use of electric potential and 2-nitrophenyl octyl ether -5% di(2-ethylhexyl) phosphate as a modified supported liquid membrane (SLM) increased the sensitivity and selectivity. The optimal extraction voltage, extraction time, and ion balance were 40 V, 10 min and 0, respectively. The dynamic linear range was 0.5-1000 ng g-1. The obtained recovery, relative standard deviation, and enrichment factor were 98%, 7%, and 35, respectively. The limits of detection 0.4 ng g-1 and the limits of quantification were obtained 1.3 ng g-1. The highest (105.0 ng g-1) and lowest (3.4 ng g-1) concentrations of nicotine were obtained for eggplant and tomato, respectively. Selective electromembrane extraction of nicotine from the donor phase to the acceptor phase was performed by optimizing the main variables influencing the method mechanism. The new channel design in this analytical system and online injection increased efficiency, stability, and repeatability. The results revealed that this method is capable for the efficient determination of trace amount of nicotine in edible vegetables.

A new chemometrically optimised HPLC method for the simultaneous determination of imatinib mesylate and capecitabine, the active medicinal components

ABSTRACT Anticancer drugs such as imatinib mesylate (IMP) and capecitabine (CAP) and their metabolites enter the water cycle through wastewater treatment plant effluents or directly into the water cycle due to their limited biodegradability in typical wastewater treatment plants. However, their long-term effects on water resources are unknown due to their toxicity. The hazards concerned with chronic exposure to these substances raise concerns about their impact on organisms, environmental safety and biodiversity conservation. Therefore, in this study, a chemometrically optimised HPLC method was developed for the simultaneous determination of trace amounts of cytotoxic agents IMP and CAP used in cancer treatment in environmental water, synthetic urine samples and drug samples. Using the Box-Behnken design, optimum conditions discovered using the traditional method were optimised. The effect of each element was evaluated in the design by four factors based on HPLC determination. For the examined levels, mobile phase 1, mobile phase 2 ratio, flow rate, and column temperature parameters for the HPLC method were determined. Using regression analysis on the experimental results, the factors influencing resolution were identified. To achieve the reliability of the results, the Analysis of Variance (ANOVA) test was used. The ANOVA test was employed to verify the consistency of the data. With the information gathered, a model was developed. HPLC was used to examine the target chemicals. A good linearity (R2 > 0.99) was established for the IMP and CAP in the concentration ranges of 1.18–23.59 µg mL−1 and 0.76–15.09 µg mL−1, respectively, under optimum circumstances. The recoveries for spiked samples at three concentration levels ranged from 98.31 to 101.11. The created method has been applied to synthetic urine samples, regional environmental water samples, and pharmaceutical samples with success.

Self-assembled flower-like carbon nanosheets for magnetic solid-phase extraction of microcystins from aquatic organism

Adsorbents with good dispersibility and high efficiency are crucial for magnetic solid-phase extraction (MSPE). In this study, flower-like magnetic nanomaterials (F-Ni@NiO@ZnO2-C) were successfully prepared by calcination of metal-organic framework (MOF) precursors that was stacked by two-dimensional (2D) nanosheet. The synthesized F-Ni@NiO@ZnO2-C has a flower-like layered structure with a large amount of pore space, promoting the rapid diffusion of targets. In addition, Zn2+ doped in MOF precursors was still retained that further produced strong metal chelation with targets. The unique structure of F-Ni@NiO@ZnO2-C was used as MSPE adsorbent, and combined with high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) for extraction of three microcystins (MCs) detection, including microcystin-LR (MC-LR), microcystin-RR (MC-RR), microcystin-YR (MC-YR). The resulting method has a detection limit of 0.2–1.0 pg mL−1, a linear dynamic range of 0.6–500.0 pg mL−1 and has good linearity (R ≥ 0.9996). Finally, the established method was applied to the highly selective enrichment of MCs in biological samples, successfully detecting trace amounts of MCs (8.4–15.0 pg mL−1) with satisfactory recovery rates (83.7–103.1 %). The results indicated that flower-like magnetic F-Ni@NiO@ZnO2-C was a promising adsorbent, providing great potential for the determination of trace amounts of MCs in biological samples.

Pseudo-Siamese network combined with label-free Raman spectroscopy for the quantification of mixed trace amounts of antibiotics in human milk: A feasibility study

The utilization of antibiotics is prevalent among lactating mothers. Hence, the rapid determination of trace amounts of antibiotics in human milk is crucial for ensuring the healthy development of infants. In this study, we constructed a human milk system containing residual doxycycline (DXC) and/or tetracycline (TC). Machine learning models and clustering algorithms were applied to classify and predict deficient concentrations of single and mixed antibiotics via label-free SERS spectra. The experimental results demonstrate that the CNN model has a recognition accuracy of 98.85% across optimal hyperparameter combinations. Furthermore, we employed Independent Component Analysis (ICA) and the pseudo-Siamese Convolutional Neural Network (pSCNN) to quantify the ratios of individual antibiotics in mixed human milk samples. Integrating the SERS technique with machine learning algorithms shows significant potential for rapid discrimination and precise quantification of single and mixed antibiotics at deficient concentrations in human milk.

One-step synthesis of a sparkling fluorescent chemodosimeter: Selective and sensitive detection of triphosgene and application in tracing triphosgene in soil

We have developed a glowing fluorescent chemodosimeter that utilizes excited-state intramolecular proton transfer (ESIPT) through a one-step synthesis process. This innovative chemodosimeter exhibited remarkable selectivity and sensitivity in detecting triphosgene, achieving a limit of detection (LOD) of 41 nM. The strong fluorescence of this probe at 504 nm was significantly quenched by triphosgene. This phenomenon is attributed to the formation of a new adduct upon the addition of guest, which restricts the ESIPT process and ultimately completely extinguishes the fluorescence. Furthermore, we have successfully extended the utility of this probe to determine trace amounts of triphosgene in soil samples of varying composition in solution and strip-based experiments. Notably, our chemodosimeter demonstrates effectiveness across a spectrum of soil types, detecting micromolar levels of triphosgene in complex soil matrices with a LOD of 1.59 µM. the promising sensing of triphosgene in complex soil system hold potential detection of extremely toxic chemical warfare presence in the environment.

3D-Printed Fluorescent Hydrogel Consisting of Conjugated Polymer and Biomacromolecule for Fast and Sensitive Detection of Cr(VI) in Vegetables.

Portable fluorescent film sensors offer a solution to the contamination issue in homogeneous sensor detection systems. However, their special structure leads to low sensitivity and a long response time, resulting in a significant scientific challenge limiting their development and application. In this work, we propose a dual design strategy to prepare highly sensitive film sensors for rapidly detecting Cr2O72-. Specifically, P(Fmoc-Osu)-SA hydrogel films were developed by integrating the biological macromolecule sodium alginate (SA) with the conjugated polymer poly(N-(9-Fluorenylmethoxycarbonyloxy)succinimide) (P(Fmoc-Osu)), using both mold and inkjet 3D printing methods. The "molecular wire effect" of the sensing unit P(Fmoc-Osu) and the water channel within the film substrate are responsible for the improved sensitivity and the reduced response time of this thin film sensor. P(Fmoc-Osu)-SA hydrogel films prepared by these two methods can rapidly detect Cr2O72- with limits of detection of 1.18 and 0.078 nM, respectively. Considering that 3D-printed hydrogel films can be tailored to different shapes according to detection needs, the P(Fmoc-Osu)-SA hydrogel films produced from this method were effectively applied in vegetable samples. This study provides an innovative and effective strategy for the development of biocompatible hydrogel sensors that offer the potential for determining trace amounts of Cr2O72- in agriculture.

Solution structure, crystal structure, Hirshfeld surface analysis of copper(II) diamide species as an optical chemical sensor

Optical chemical sensors are promising tools for the detection of metal ions in various samples. Copper(II) has received significant attention among metal ions due to its toxic nature and widespread applications in various industrial processes. In recent years, several optical chemical sensors have been developed to detect copper(II) with high sensitivity and selectivity. This paper describes the spectrophotometric determination of trace amounts of copper(II) using N1-(2-aminoethyl)-N2-((pyridin-2-yl)methyl)oxalamide (H2(555)NH2) as an optical chemical sensor. The protonation and formation constants of the Cu(II)/(H2(555)NH2) system were determined at 25 °C and the ionic strength of 0.15 mol dm−3 using glass electrode potentiometry. The structures of the different species, present in solution at different pH values, were determined using UV–vis, 1H NMR, and EPR spectroscopic techniques. At pH 5, the [Cu(H2(555)NH2)]2+ species was formed with the Cu(II) coordinated to the pyridole nitrogen and the terminal amine. Above pH 8, [Cu(H2(555)NH2)H-2] is the most predominant species in solution. Here the Cu(II) coordinates to all four nitrogen atoms. In the solid state, a dinuclear complex, [Cu(H(55)NH3)Cl]2[Cu(H2O)2(NO3)2Cl2]H2O, was formed. Single crystal X-ray structure showed the Cu(II) to be coordinated to the pyridine and the amide N-atoms in addition to an O-atom from one of the two carbonyl groups. The coordination environment was completed by two bridged chloride ions to give a slightly distorted trigonal bipyramidal coordination geometry around the copper centre. The amine was not coordinated. The proposed sensor was successfully applied to determine copper(II) in real samples, with recoveries ranging from 10−5 to 10−3 mol/dm−3. Using H2(555)NH2 as an optical chemical sensor emerged as a powerful tool for detecting copper(II) ions in different aqueous samples.

A novel colormetric and light-up fluorescent sensor from flavonol derivative grafted cellulose for rapid and sensitive detection of Hg2+ and its applications in biological and environmental system

Mercury ion (Hg2+) is one of harmful heavy metal ions that can accumulate inside the human organism and cause some health problems. In the article, a highly effective fluorescent probe named EC-T-PCBM was prepared by grafting flavonol derivatives onto ethyl cellulose for the specific recognition of Hg2+. EC-T-PCBM exhibited a remarkable fluorescence light-up response toward Hg2+ with excellent sensitivity. EC-T-PCBM possessed several prominent sensing properties for Hg2+, such as low detection limit (43.9 nM), short response time (5 min), and wide detection pH range (6–9). The response mechanism of EC-T-PCBM to Hg2+ has been verified through 1H NMR titration and DFT computation. Additionally, EC-T-PCBM not only can be used for accurately determining trace amount of Hg2+ in actual environmental water samples, but also can serve as a portable and rapid device by loading it on test strips for sensitive and selective visualization of Hg2+. More importantly, the confocal fluorescence imaging of onion cells suggested the favorable cell membrane permeability of EC-T-PCBM and its prominent ability to continuously monitor the enrichment from Hg2+ within fresh plant tissues.

Unveiling Morphine: A Rapid and Selective Fluorescence Sensor for Forensic and Medical Analysis.

Opioid use, particularly morphine, is linked to CNS-related disorders, comorbidities, and premature death. Morphine, a widely abused opioid, poses a significant global health threat and serves as a key metabolite in various opioids. Here, we present a turn-off fluorescent sensor capable of detecting morphine with exceptional sensitivity and speed in various samples. The fluorescent sensor was developed through the dimerization process of 7-methoxy-1-tetralone and subsequent demethylation to produce the final product. Despite morphine possessing inherent fluorophoric properties and emitting light in an approximately similar wavelength as the sensor's fluorescent blue light, the introduction of the target molecule (morphine) in the presence of the sensor caused a reduction in the sensor's fluorescence intensity, which is attributable to the formation of the sensor-morphine complex. By utilizing this fluorescence quenching sensor, the chemo-selective detection of morphine becomes highly feasible, encompassing a linear range from 0.008 to 40 ppm with an impressive limit of detection of 8 ppb. Consequently, this molecular probe demonstrates a successful application in determining trace amounts of morphine within urine, yielding satisfactory analytical results. The study also explores the effect of several variables on the sensor's response and optimizes the detection of morphine in urine using a response surface methodology with a central composite design.

Novel LC-MS/MS Method for Simultaneous Determination of Monoamine Neurotransmitters and Metabolites in Human Samples.

For the simultaneous determination of monoamine neurotransmitters (NTs) like dopamine, serotonin, noradrenaline, and epinephrine, and their metabolites (metanephrine, normetanephrine, 3-methoxytyramine, vanillylmandelic acid, 3,4-dihydroxyphenylacetic acid, homovanillic acid, and 5-hydroxyindoleacetic acid), a robust liquid chromatography method coupled with tandem mass spectrometry (LC-MS/MS) was introduced as the analytical method. This analytical method proved to be accurate for the simultaneous measurement of the amounts of 11 NTs and their metabolites in biological samples. The method proved to be more efficient and better than the previously reported method in terms of precision, recovery, sample requirement, and extraction procedure. The reported method requires only 100 μL of blood and 200 μL of urine, and the extraction procedure requires acetonitrile precipitation, filtration, drying, and reconstitution in water. The separation of all analytes was performed on an C18 column (4.6 mm × 150 mm and 1.8 μm). A 10 min gradient elution program with a mobile phase consisting of phase A (0.2% formic acid in water) and phase B (methanol) was used. The positive ionization mode was used for the detection of all analytes in multiple reaction monitoring (MRM). The proposed method was validated with an internal standard and yielded lower limits of detection and quantification ranges of 0.0182-0.0797 ng/mL and 0.0553-0.2415 ng/mL, respectively, with a good linearity (R2) between 0.9959 and 0.9994. The recoveries ranged from 73.37% to 116.63% in blood and from 80.9% to 115.33% in urine. For the NTs and metabolites, the intra- and interday % CV were 0.24-9.36 and 0.85-9.67, respectively. The developed LC-MS/MS method was successfully used for the determination of trace amounts of endogenous compounds in human blood and urine samples.

A smartphone-based colorimetric assay using Cu-tannic acid nanosheets (Cu-TA NShs) as a laccase-mimicking nanozyme for visual detection of quercetin in vegetables.

Theinteraction of Cu-tannic acid nanosheets (Cu-TA NShs) as nanozyme in a surfactant solution of CTAB under relatively acidic conditions is shown toexhibit a catalytic effect on quercetin (Qur). This catalytic property of Cu-TA NShs, which mimics laccase enzyme with many advantages, has been applied todeveloping a selective colorimetric sensor for the determination of trace amounts of Qur in vegetable samples. This strategy presents a desirable linear relationship between the absorbance signal intensity and the concentrations of Qur from 0.350 to 32.09 µM with a detection limit (LOD) of 0.064 µM (S/N = 3). The feasibility of the proposed portable colorimetric sensor for in situ analysis of the real samples has been validated with the high-performance liquid chromatography (HPLC) method as reference method, and two-tailed test (t test) statistical analysis certifies good agreement between the results. This enzyme-free and sensitive naked-eye sensor with the smartphone-based color map is promising to provide technical support for the rapid and visual detection of Qur in vegetables.

Multiwall Carbon Nanotubes/Spherical Glassy Carbon as Environmentally Friendly Adsorption Materials Utilized in Adsorptive Stripping Voltammetry for the Determination of Trace Amounts of Ga(III).

This work presents a proposal for an adsorptive stripping voltammetric (AdSV) method for gallium(III) determination at an eco-friendly multiwall carbon nanotube/spherical glassy carbon (MWCNT/SGC) electrode modified with a lead film. The operational factors influencing the sensitivity of the AdSV procedure were thoroughly investigated, and their most favorable values were chosen (0.1 mol L-1 acetate buffer solution pH = 5.6; 7 × 10-5 mol L-1 Pb(II); 2 × 10-4 mol L-1 cupferron; potential/time of lead film formation: -1.9 V/30 s; potential/time of Ga(III)-cupferron adsorption: -0.75 V/30 s). The newly developed MWCNT/SGCE has proven to be a competitive substrate to the glassy carbon electrode to create a lead film electrode, since it allows the determination of gallium in a wider range of concentrations from 3 × 10-9 to 4 × 10-7 mol L-1 with a lower limit of detection equal to 9.5 × 10-10 mol L-1. The elaborated procedure has been shown to be highly selective and insensitive to the presence of an even 100-fold excess of most of the ions commonly found in environmental waters. The MWCNT/SGC sensor, which can maintain >95% of its original response after 70 days of use, has been successfully applied for the detection of gallium in water samples with the relative standard deviation (RSD) ranging from 4.5% to 6.2% (n = 3) and recoveries in the range from 95.3% to 104.9%.

A portable fluorescence detection device based on a smartphone employing carbon nanodots for Mn2+ sensing.

The measurement of fluorescence emission for quantitative analysis is typically based on a traditional spectrofluorometer, which limits an onsite detection approach. Thus, an alternative device should be developed for fulfilling this analysis outside of the laboratory. Therefore, a low-cost, portable, and low-energy consumption fluorescence reader-based smartphone device was developed. An ultraviolet light-emitting diodes (UV-LED) was used to construct the fluorescence device-based smartphone as a low-power excitation light source. The smartphone camera was used as a detector for detecting photons from the fluorescence emission process of the fluorescence probe and was connected to a digital image platform. Transparent acrylic with orange and yellow colors was employed as a filter for reducing the interference from light source intensity. The obtained digital image was converted to red, green and blue (RGB) intensity using a custom-designed smartphone application. N,S-doped carbon nanodots (N,S-CDs) were demonstrated to be a good fluorescence indicator for determining trace quantities of Mn2+ in cosmetics. The approach exhibited high selectivity and sensitivity, detecting and quantifying analytes at 1-5 μM concentrations. Furthermore, the method's detection limit of 0.5 μM reflects its capacity to detect trace amounts of a target analyte. Mn2+ in cosmetic products was successfully analyzed using this device with high accuracy comparable with the results from inductively coupled plasma-optical emission spectroscopy (ICP-OES).

Preconcentration and measurement of trace Amitriptyline hydrochloride in water samples using magnetic nanoparticles with dispersive solid‐phase extraction

AbstractIn the separation and determination of trace amounts of drugs in aqueous samples, there is a major challenge in synthesizing highly efficient, cost‐effective, and easy‐to‐use adsorbents based on natural polymers, which are also biocompatible and biodegradable. In the proposed method, magnetite nanoparticles (Fe3O4) on chitosan (as the carrier) modified with β‐cyclodextrin (BCD) were used as a suitable adsorbent for the pre‐concentration and solid‐phase extraction of trace amounts of Amitriptyline HCl (hydrochloride). Ultraviolet spectrophotometer (λ = 236 nm) was the main instrument used for analyte detection and quantification. Moreover, X‐ray diffraction, Fourier transform infrared spectroscopy, Field Emission Scanning Electron Microscopy, and Energy‐Dispersive X‐ray were used for the identification and characterization of the structure and morphology of the adsorbent and to establish the formation of the synthesized magnetic nanosorbents, as well as to confirm the analyte binding to the adsorbent. Experimental variables affecting the extraction/pre‐concentration and determination of the analyte were investigated and optimized; pH of the sample solution, the amount of NaCl salt (in terms of ionic strength of the solution), the amount of adsorbent, temperature, adsorption time, and volume of the eluent (methanol) were the optimized parameters. Finally, the method was successfully applied for the determination of spiked Amitriptyline hydrochloride (HCl) in tap water and human urine samples. Also, High‐Performance Liquid Chromatography was performed on the aqueous samples to compare the proposed method with the USP (the United States Pharmacopeia) standard method of Amitriptyline HCl assay and after performing a t‐test (confidence level of 95%), no significant difference was observed between the two methods. High accuracy and precision (RSD = 3.91%), High analysis speed, few limitations, low expenses, pure extracted analyte, and low waste were the advantages of this method. This method was also compatible with many existing device methods. Under the optimized experimental conditions, the calibration graph was linear in the range of 0.183 to 50 mg.L−1 with a correlation coefficient of 0.996. RSD of the method was 3.91%, the limit of detection was 37.8 µg.L−1, the maximum sorption capacity of the adsorbent for Amitriptyline hydrochloride was 306.525 mg.g−1 and the preconcentration factor was 3.61. Eventually, the proposed method was compared to other methods that have been performed for the determination of Amitriptyline hydrochloride.

Determination of iron in water by flame atomic absorption spectrometry with sorption preconcentration

Determination and monitoring of pollutants in the natural environment is an urgent task because of their impact on living organisms as a result of numerous anthropogenic impacts. For this reason, a large number of publications are devoted to the development, modification or optimization of analytical methods that can solve these problems. When determining trace elements present in various samples, such as natural and waste water, biological samples and alloy samples, direct determination by various instrumental methods is often impossible due to the matrix effect and rather low concentration of metal ions in the sample. The atomic absorption method is one of the methods widely used for the determination of iron ions, which has such advantages as simplified sample preparation, low probability of contamination and loss of elements, increased analytical productivity, the detection limit of components in the analyzed mixture reduced by several orders of magnitude, and the ability to determine trace amounts of elements in small samples. The aim of the study was to develop a technique for the preliminary concentration of Fe (III) ions in waters of various origins using a sorbent immobilized with sulfosalicylic acid and their further determination by flame atomic absorption spectrometry. Sorbents obtained on the basis of polyacrylonitrile modified with polyethylene polyamine (PPF-1 and PPA-1) with sulfosalicylic acid immobilized on their surface were used for selective sorption of Fe (III) ions. Optimal conditions for the immobilization of sulfosalicylic acid on sorbents and the formation of complexes with Fe (III) ions were studied. The developed sorption-atomic absorption technique provided determination of low concentrations of Fe (III) ions in various waters. The use of PPF-1 as a sorbent with immobilized sulfosalicylic acid for pre-concentration of iron has a number of advantages compared to traditional atomic absorption procedure, i.e., the simplicity, high degree of iron extraction, high sensitivity and selectivity of iron determination, as well as a low cost. The detection limit of iron ions is 0.01 μg/L, Sr does not exceed 0.033.

Ecofriendly ratiometric colorimetric determination of mercury(II) ion in environmental water samples using gallic acid-capped gold nanoparticles

Today, the monitoring and determination of heavy metal pollutants in the environment is an essential requirement for the environmental and research communities. Mercury ion is one of the most hazardous heavy metals, and scientists are trying to develop new methods for its detection. In this study, a new colorimetric sensor based on aggregation gallic acid-capped gold nanoparticles (GA-AuNPs) for the determination of mercury ions in environmental water samples was presented. The green synthesized GA-AuNPs exhibited a sharp surface plasmon resonance peak at 515 nm. The addition of mercury ions changed the surface properties of GA-AuNPs, resulting in the formation of a new peak near 670 nm due to the aggregation of GA-AuNPs, and an obvious color change from red to purple occurred. Thus, mercury ions were detected based on the change in the absorbance ratio (A670/A515). The developed sensor can determine the mercury ions in the concentration range of 78.0 nM to 8.3 µM with a detection limit of 5.5 nM. Based on the Environmental Protection Agency (EPA) and the World Health Organization (WHO) reports, the amount of Hg2+ ions in fresh water should be between 10.0 and 30.0 nM. The results indicate that the developed sensor can detect and determine trace amounts of Hg2+ ions in environmental water samples.

Dual-chromic cellulose paper modified with nanocapsules containing leuco dye and spiropyran derivatives: A colorimetric portable chemosensor for detection of some heavy metal cations

Heavy metal cations are important in our daily life and may cause serious disorders and diseases. Colorimetric portable cellulosic sensors with high selectivity and sensitivity toward metal cations are preferred relative to those based on small molecules which operate mostly in organic media and difficult test methods. Here, dual-chromic stimuli-responsive cellulose paper (TPL@T-Cell) was produced by modification of the paper with the designed and prepared epoxy-functionalized polyacrylic nanocapsules via dip-coating and subsequent heat treatment processes. The capsules contained thermochromic leuco-dye derivative and photochromic hydroxyl-functionalized spiropyran and were prepared through semi-continuous miniemulsion polymerization. Chemical structure of the synthesized dyes, nanocapsules and modified cellulose fibers were identified by FTIR and UV-Vis analyses. Spherical morphology of the prepared nanocapsules with average particles size of 121 nm were observed by SEM and DLS analyses. The effective wetting of the cellulose fibers by nanocapsules with proper diffusion and deposition through the establishment of physical and chemical interactions were evaluated by SEM and ATR-FTIR analyses, respectively. The prepared TPL@T-Cell sensor revealed distinct color changes toward Fe2+, Pb2+ and Sn2+ ions. Opto-chemical results indicated that detection limit of TPL@T-Cell for Sn2+ (0.0028 µM, 0.326 ppb), Fe2+ (0.0013 µM, 0.15 ppb), and Pb2+ (0.0023 µM, 0.268 ppb) are lower than their critical permitted levels announced by WHO. These exhibited applicability of TPL@T-Cell sensor for determining trace amount of some heavy metal ions with instant responsivity, wide linear detection range, high sensitivity, and low detection limit via colorimetric and spectroscopic responses.

Trace mercury in wate were measured by dispersion-liquid microextraction combined with spectrophotometry

An experimental method was developed for the determination of trace amounts of mercury by dispersion-liquid microextraction combined with spectrophotometry. Undea buffer medium of hydrochloric acid and sodium acetate at pH=4, mrcury ions in the water were extracted by dispersion-liquid microextraction at the wavelength of 410nm, carbon tetrachloride was used as an extractant, methanol was used as a dispersant, dithizone-methanol solution was used as a chelating agent, the optimum conditions for extraction were obtained, Carbon tetrachloride 70uL, methanol 0.75mL, dithizone methanol solution 200uL. Under the optimal conditions, Lambert-Beer's law was satisfied at concentrations of 0.1-20μg/L,the detection limit is 64.2ng /L, The correlation coefficient of the standard curve was R2 =0.9983, the relative deviation was about 4.64%. Three water samples were measured, the recoveries were 96.8%-109.2%.

Voltammetry in Determination of Trace Amounts of Lanthanides—A Review

This paper presents an overview of approaches proposed in the scientific literature for the voltammetric determination of rare earth elements (mainly cerium and europium individually, as well as various lanthanides simultaneously) in manifold kinds of samples. The work is divided into chapters describing the most important aspects affecting the sensitivity of the proposed methods: the technique adopted (AdSV, ASV, CSV), complexing agents used, the kind of working electrode (mercury-based, noble metal or carbon electrodes) and the most popular electrode modifiers (e.g., metal film, carbon nanotubes, molecularly imprinted polymers). Analytical parameters of the procedures presented in the paper are collected in tables. The subsequent chapters are devoted to a detailed discussion of potential inorganic and organic interfering factors. The possibilities of simultaneous determination of several lanthanides in one sample and the influence of other lanthanides on the determined rare earth element were also discussed. Finally, the applications of the voltammetric procedures to the determination of rare earth metals in real samples with miscellaneous matrix is described. All analytical results were tabulated in order to compare the analytical suitability of the proposed procedures.

CATALASE AND PEROXIDASE BIOMIMETIC SENSOR BASED ON Ag-ELECTRODE

Research has been carried out on the development of a biomimetic sensor of the catalase and peroxidase type to determine trace amounts of peroxide hydrogen and low concentrations of ethyl alcohol in an aqueous solution. By potentiometric research, the physicochemical feature of the catalase and peroxidase biomimetic sensor was studied, the transducer of which was Ag. Rapid and accurate determination of hydrogen peroxide is very important, but no less important side of this issue is associated with the determination of trace amounts of C2H5OH in aqueous media of various origins. The need to develop express methods for determining the concentration of C2H5OH in aqueous solutions follows from the requirements for the quality of wine and alcohol products. As you know, the taste and drinking qualities of the product depend on the ratio of methyl and ethyl alcohols. In this work, biomimetic sensors of the catalase and peroxidase types based on an Ag electrode were developed for determining trace amounts of hydrogen peroxide and ethanol. Biomimetic sensors of the catalase and peroxidase types based on an Ag electrode have been developed for the determination of microquantities of hydrogen peroxide and ethyl alcohol. The applicability of a biomimetic sensor for determining trace concentrations of hydrogen peroxide, as well as for determining microquantities of ethyl alcohol in an aqueous solution with a low detection limit, high sensitivity, wide recognition range, high stability, and repeated use, is shown. The developed and synthesized biomimetic sensor of the catalase and peroxidase types based on TPhPFe3+/Al2O3/Ag have high sensitivity, stability, and do not lose their activity for a long time