Removal of Ni(II), Cu(II), Pb(II), and Cd(II) from Aqueous Phases by Silver Nanoparticles and Magnetic Nanoparticles/Nanocomposites.

The intake of heavy metals into the body, even at very low concentrations, may cause a decrease in central nervous system functions; deterioration of blood composition; and liver, kidney, and lung damage. Therefore, heavy metal ions must be removed from water. In this study, silver, magnetic iron/copper, and iron oxide nanoparticles were synthesized using Lathyrus brachypterus extract and then Fe/Cu-AT, Fe3O4-AT, Fe/Cu-CS, and Fe3O4-CS magnetic nanocomposite beads were synthesized using alginate and chitosan. The removal of Cd(II), Pb(II), Ni(II), and Cu(II) ions from aqueous phases using synthesized nanoadsorbents was investigated by single and competitive (double and quaternary) adsorption techniques. The kinetic usability of the magnetic iron oxide chitosan (Fe3O4-CS) nanocomposite beads with the highest removal efficiency was evaluated. Based on experimental results, the order of removal was found to be 98.39, 75.52, 51.54, and 45.34%, and it was listed as Pb(II) > Cu(II) > Cd(II) > Ni(II), respectively. The Dubinin-Radushkevich, Freundlich, Langmuir, and Temkin isotherm models were used, and experimental results revealed that the experimental data fit the Langmuir model better. The maximum adsorption capacities (qm) obtained from the Langmuir isotherm model of Fe3O4-CS were found to be 8.71, 23.75, 18.57, and 12.38 mg/g for Ni(II), Pb(II), Cu(II), and Cd(II) ions, respectively. When the kinetic data were applied to the Lagergren, Ho-McKay, and Elovich models, it was observed that the adsorption kinetics mostly conformed to the Ho-McKay second-order rate equation. The binary and quaternary competitive adsorption data showed that Fe3O4-CS were selective toward Cu(II) and Pb(II). The reusability of the Fe3O4-CS nanoadsorbent was performed as three cycles with the same concentration. The adsorption capacities were found to be 95.81, 70.65, 50.50, and 42.75%, in turn for Pb(II), Cu(II), Cd(II), and Ni(II) ions after three cycles, which revealed that the Fe3O4-CS nanoadsorbent can be used after three cycles without losing its efficiency.

Development of a New Sensitive Method for Lead Determination by Platinum-Coated Tungsten-Coil Hydride Generation Atomic Absorption Spectrometry.

A novel very sensitive and rapid analytical method was improved where gaseous lead formed was transported to and trapped on an externally heated platinum-coated tungsten-coil atom trap for in situ preconcentration. The analytical performance of the developed method with the graphite furnace atomic absorption spectrometry (GFAAS) method was compared. All critical parameters affecting the performance of both methods were optimized. The limit of quantitation (LOQ) was found as 11.0 ng L-1 and the precision was 2.3% in terms of percent relative standard deviation (RSD%). Characteristic concentration (Co) of the developed trap method was indicating a 32.5-fold enhancement in sensitivity compared to the GFAAS method. In order to investigate the surface morphology of the W-coil, scanning electron microscope-energy-dispersive X-ray (SEM-EDS) analyzes were performed. The accuracy of the trap method was tested by certified reference materials: NIST SRM 1640a (the elements in natural water) and DOLT:5 (dogfish liver). Interferences from other hydride-forming elements were investigated. Application of the trap method was demonstrated by the analysis of some drinking water and fish tissue samples. The t test was applied to drinking water samples, and the results indicated that there was no statistically significant error.

Development of a Sensitive Method for Cadmium Determination in Fish Tissue and Drinking Water Samples by FAAS Using SQT In Situ Atom Trapping.

A sensitive and robust trap method was developed for the determination of cadmium (Cd) by using a slotted quartz tube. Using this method at a sample suction rate of 7.4 mL/min for 4.0 min collection, a 1467-fold increase in sensitivity was obtained compared to the flame atomic absorption spectrometry method. Under the optimized conditions, a limit of detection of 0.075 ng mL-1 was obtained for the trap method. The interference effects of hydride-forming elements, transition metals, and some anions on the Cd signal were investigated. The developed method was evaluated by analyzing "Sewage Sludge-industrial origin (BCR no: 146R)", "NIST SRM 1640a Trace elements in natural water", and "DOLT: 5 Dogfish Liver". There was a good agreement between the certified and found values at the 95% confidence level. This method was applied successfully for the determination of Cd in drinking water and some fish tissue samples (liver, muscle, and gill) obtained from Mugla province.

Determination and speciation of methyl mercury and total mercury in fish tissue samples by gold-coated W-coil atom trap cold vapor atomic absorption spectrometry.

A sensitive analytical technique was developed where gaseous mercury formed by sodium tetrahydroborate reduction is transported to and trapped on a resistively heated gold-coated Tungsten-coil atom trap for in situ preconcentration. This technique was applied successfully for determination and speciation of methyl mercury and total mercury in some fish tissue samples (liver, muscle and gill) obtained from Mugla province. The analytical parameters were optimized both for trap and no-trap studies. Under the optimized conditions, a limit of detection (LOD) of 6.0 ng/L was obtained. The precision was evaluated by relative standard deviation (RSD%) corresponding to 4.1% (n = 11). Accuracy of the proposed method was evaluated by analyzing "DOLT:5 Dogfish Liver", "NIST SRM 1640a Trace elements in natural water" and "NIST 1946 Lake Superior fish tissues". The measurements of the certified reference materials were in good agreement with the certified values at the 95% confidence level.

Speciation and determination of inorganic selenium species in certain fish and food samples by gold-coated W-coil atom trap hydride generation atomic absorption spectrometry.

A very sensitive, selective, rapid and easy gas-phase preconcentration based method is presented for the determination and speciation of inorganic selenium in chicken meat, poultry eggs, mullet fish (Mugil Cephalus) and sea bass fish (Dicentrarchus Labrax) samples. Gold-coated W-coil atom trap was used to increase the sensitivity of conventional HG-AAS. LOD and LOQ values were calculated to be 0.021 µg/L and 0.070 µg/L, respectively. RSD% was found as 3.24. The sensitivity was increased 20 times more with the method used in the current study than the HG-AAS method. The interference effects of other metals on Se signal were significantly reduced by trap. SEM and EDX images of both bare and gold coated W-coil atom trap were screened. In order to check the accuracy of the method, "DOLT-5: Dogfish Liver" standard reference material was used and there was a good agreement between certified and found values at the 95% confidence level.