Cadmium Ions In Water Samples Research Articles

Evaluation of PVC@Silver Nanocomposite as Sensor for Low Limit Detection of Cadmium Ion By Surface Plasmon Resonance Based Method

This study explores the development of a PVC@Silver nanocomposite for enhanced detection of cadmium ions in water samples. Various characterization techniques confirmed the successful incorporation of silver nanoparticles into the polyvinyl chloride (PVC) matrix across different concentrations (1–4%). X-ray diffraction revealed the face-centered cubic crystalline structure of the silver nanoparticles, with the intensities of the (111), (200), (220), and (311) peaks increasing with higher Ag concentrations. The average crystallite sizes ranged from 26.1 nm (3% Ag) to 30.0 nm (2% Ag). Dynamic light scattering showed nanoparticle sizes of 24–43 nm, while zeta potential values of -24 to -40 mV indicated reasonable colloidal stability. Brunauer–Emmett–Teller (BET) surface area analysis demonstrated a decreasing surface area from 30.09 m2/g (1% Ag) to 25.27 m2/g (3% Ag), attributed to pore filling by silver nanostructures. Significantly, the PVC@Silver nanocomposite facilitated sensitive detection of Cd(II) ions using surface plasmon resonance (SPR), exhibiting an SPR angle shift of 26.30° with intensity values ranging from 10.80 (4% Ag) to 12.19 (3% Ag). UV–vis spectra revealed a prominent surface plasmon resonance band at 420–430 nm, indicating the presence of silver nanoparticles. The optical band gap varied from 4.51eV (1% Ag) to 4.12eV (4% Ag).

ZIF-12 @ polypyrrole nanowires for selective detection of cadmium ions in water samples

Cadmium ion detection is an important area of research since it is associated with numerous diseases in humans and the environment. In this study, selective Cd2+ ion detection using polypyrrole and ZIF-12 was investigated using the square wave voltammetry technique. A convenient chemical method is used to polymerize the pyrrole to form a composite, which provides a better electroactive surface area of 24.5 x 10-3 m2 for the ZIF-12@Ppy composite modified GCE. The –NH2 functional group in polypyrrole makes good adsorptive property for Cd2+ ion capture with a detection range of 10 µM to 5 mM, the regression equation of y = 0.0102 x + 43.289, and low detection limit of approximately 50 nM as a result of enhanced electrocatalytic activity. The good anti-interference properties, repeatability, and stability of the prepared composite successfully demonstrated for the detection of Cd2+ ions in real samples from various water sources. Overall, these studies provide good insights into the development of an effective device for the detection of Cd2+ ions using polypyrrole and ZIF-12 platform.

Application of a Novel Ion-Imprinted Polymer to the Separation of Traces of CdII Ions in Natural Water: Optimization by Box-Behnken Design

This study describes the preparation of a novel ion-imprinted polymer (IIP) to apply pre-concentration of cadmium ions in water samples of the Pontal Bay in Ilheus, Brazil. First, cadmium ion was complexed with 2-(2-thiazolylazo)-p-cresol (TAC). Subsequently, there was the polymerization using ethylene glycol dimethacrylate and methacrylic acid monomers along with the radical azobisisobutyronitrile initiator. The mold ions were removed using 2:1 (v v-1) nitric acid. The thermal stability of the polymer was evaluated by thermogravimetry and the characterization was performed by Fourier transform infrared spectroscopy. The maximum adsorption capacity for IIP (qmax = 84.75 mg g-1) could be described by the Langmuir isotherm. The variables: sample flow rate, pH and eluent (nitric acid) were optimized using Box-Behnken design with determination by flame atomic absorption spectrometry (FAAS). The enrichment factor, as well as the limits of detection and quantification (LOQ), were found to be 44, 0.14 and 0.46 µg L-1, respectively. Selectivity was evaluated by using solutions containing CdII, CuII, NiII, PbII, CoII, SO42-, and Cl- ions. The concentration of cadmium ions in the samples varied between < LOQ to 1.25 µg L-1.

Synthesis and Characterization of Porous MnCo2O4 for Electrochemical Determination of Cadmium ions in Water Samples

To utilize the maximum activity of nanomaterials, it was specifically synthesized by appropriate physicochemical properties. In that aspect, we have described the synthesis of porous MnCo2O4 by simple chemical route and applied for the selective detection of cadmium (Cd (II)). The as-prepared porous MnCo2O4 was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET) adsorption isotherm, X-ray diffraction pattern analysis (XRD), Fourier transform infra-red spectroscopy (FT-IR), energy dispersive X-ray (EDX) and electrochemical techniques. The porous MnCo2O4 exhibited an excellent electrochemical behaviour and good analytical response towards the determination of Cd (II). Those analytical factors such as pH, deposition potential and deposition time are optimized by using differential pulse anodic stripping voltammetry (DPASV). A wide linear concentration range from 2.3 to 120 µg L−1, limit of detection (LOD) of 0.72 µg L−1 and the limit of quantification (LOQ) of 0.91 µg L−1 were achieved for determination of Cd (II). The selectivity of the developed sensor was explored in the presence of co-interfering ions. Also our sensor exhibits a good stability, reproducibility and repeatability. In addition, the practicability of proposed sensor was evaluated for the detection of Cd (II) in real water samples.

Determination of copper, nickel, manganese and cadmium ions in aqueous samples by flame atomic absorption spectrometry after simultaneous coprecipitation with Co(OH)2

A separation-preconcentration procedure was developed for the determination of trace amounts of copper, nickel, manganese and cadmium ions in water samples by flame atomic absorption spectrometry after coprecipitation by Co(OH)2 as a carrier without a chelating agent. The influence of the various analytical parameters such as pH, amount of carrier reagent, standing time, centrifugation rate and time, sample volume and matrix effects on the recovery of the analyte ions was studied. Under the specified experimental conditions the calibration curves for Ni(II) and Cu(II) were linear from 0.5 to 200ngmL−1 and for Mn(II) and Cd(II) from 0.5 to 250 and 0.3 to 80ngmL−1, respectively. The relative standard deviations for seven replicate determinations of a mixture of 40.0ngmL−1 of Cu(II), Ni(II), Mn(II) and 20ngmL−1 of Cd(II) in the original solution were 1.9%, 1.7%, 1.8% and 2.1%, respectively. The detection limits based on 3Sb/m for Cu(II), Ni(II), Mn(II) and Cd(II) in the original solution were 0.2, 0.2, 0.3 and 0.07ngmL−1, respectively. The limits of quantification based on 10Sb/m for Cu(II), Ni(II), Mn(II) and Cd(II) in the original solution were 6.7, 6.7, 10.0 and 2.3ngmL−1, respectively. The proposed method has been applied to the determination of trace amounts of the analyte ions in two certified reference materials (the National Institute for Environment Studies (NIES) No. 1 Pepperbush and NIES No. 7 Tea Leaves) and water samples and satisfactory results were obtained.

Poly(crystal violet)/graphene-modified electrode for the simultaneous determination of trace lead and cadmium ions in water samples

A novel poly(crystal violet)/graphene-modified glassy carbon electrode (PCV/Gr/GCE) was fabricated for the simultaneous determination of Pb2+ and Cd2+. The electrochemical behavior of both species at the PCV/Gr/GCE was investigated employing cyclic voltammetry. In acetate buffer, the modified electrode showed an excellent electrocatalytical effect on the oxidation of both species and was further used for their determination. Under optimized analytical conditions, the oxidation peak currents of Pb2+ and Cd2+ obtained by differential pulse voltammetry in pH 4.6 acetate buffer showed a linear relationship with their concentrations in the ranges of 2.00 × 10−8–1.95 × 10−5 mol L−1 and 4.00 × 10−8–5.58 × 10−5 mol L−1, respectively. The developed method has excellent sensitivity, selectivity, reproducibility and has been successfully applied to the determination of Pb2+ and Cd2+ in water samples.

Cadmium (II)-selective electrode based on palm shell activated carbon modified with task-specific ionic liquid: kinetics and analytical applications

In this study, palm shell activated carbon modified with task-specific ionic liquid was used as a novel electrode component for the potentiometric determination of cadmium ions in water samples. The proposed potentiometric sensor has good operating characteristics, including relatively high selectivity towards the Cd (II) ion, a Nernstian response to Cd (II) ions in a working concentration range of 1.0 × 10−9–1.0 × 10−2 M, with a reasonable detection limit of 1 × 10−10 M and a slope of 30.90 ± 1.0 mV/decade. No significant changes in electrode potential were observed when the pH was varied over the range of 4–9. A direct technique based on the use of ion-selective electrode potentiometry has been developed in our laboratory for the study of reaction kinetics and kinetic methods of analysis by continuous monitoring of the rate of production or consumption of an ion. The apparent adsorption rate constant was estimated assuming pseudo-second-order kinetics. Additionally, the proposed electrode has been successfully used for the determination of the cadmium content in real samples without a significant interaction from other cationic or anionic species.

Dispersive micro solid-phase extraction using multiwalled carbon nanotubes combined with portable total-reflection X-ray fluorescence spectrometry for the determination of trace amounts of Pb and Cd in water samples

In this paper the combination of dispersive micro solid-phase extraction (DMSPE), using multiwalled carbon nanotubes (MWCNTs) as solid sorbents, with total-reflection X-ray fluorescence spectrometry (TXRF) is proposed for preconcentration and determination of lead and cadmium ions in water samples. The proposed sample preparation is quite simple and economic. After the sorption processes of the metals on the MWCNTs, the aqueous sample is separated by centrifugation and the metal loaded MWCNTs are suspended using a small volume of an internal standard solution and analyzed directly by TXRF. Parameters affecting the extraction process (complexing agent, pH of the aqueous sample, amount of MWCNTs) and TXRF analysis (volume of the deposited suspension on the reflector, drying mode, and instrumental parameters) have been carefully evaluated to test the real capability of the developed methodology for the determination of Cd and Pb at trace levels. For both elements the linear range is observed up to 50 ng mL−1. Under optimized conditions detection limits are 1.0 ng mL−1 and 2.1 ng mL−1 for Cd(II) and Pb(II) ions, respectively. Both of the examined elements can be determined with quantitative recoveries (ca. 100%) and with an adequate precision (RSD = 6.0% and 10.5% for Cd(II) and Pb(II), respectively). Our results give insight into the possibilities of the combination of DMSPE and TXRF for trace metal determination in different types of environmental waters (sea, river and waste water).