A sensitive and accurate analytical method for the determination of cadmium in food samples: Molybdenum coated T-shape slotted quartz tube flame atomic absorption spectrophotometry.

In this study, a molybdenum coated T-shaped slotted quartz tube atom trap flame atomic absorption spectrophotometry method (Mo coated-T-SQT-AT-FAAS) was developed for the determination of cadmium with on-line preconcentration. Inner surface of T-SQT was coated with molybdenum to enhance the trapping efficiency. Hydrogen gas was used instead of organic solvents to release trapped atoms. Limit of detection and quantification were found to be 0.057 and 0.082 µg/L, respectively. The developed method has a linear working range between 0.10 and 1.0 µg/L with a low %RSD value (<3.7). About 1202 times enhancement in detection power was recorded over the conventional FAAS system. Recovery experiments were used to determine the applicability of the method developed to real samples (linden, milk powder and mint) and significant results (94.4-100.7%) were obtained for the samples spiked at 0.30, 0.50 and 1.0 µg/L. The method was also applied to Tomato Leaves 1573a SRM to check the accuracy.

A new combination for the determination of ultratrace cadmium: solid-phase microextraction by stearic acid-coated magnetic nanoparticles prior to batch-type hydride generation atomic absorption spectrometry.

Solid-phase microextraction method based on stearic acid-coated magnetic nanoparticle has been combined with batch-type hydride generation atomic absorption spectrometry (BT-HGAAS) system to determine cadmium at ultratrace levels. After the adsorption of cadmium ions onto stearic acid-coated magnetic nanoparticles, they were easily separated from the aqueous phase by means of a magnet. All the instrumental and experimental parameters such as pH of buffer solution, interaction period, concentration, and volume of NaBH4 were optimized. Under the optimal conditions, limit of quantification (LOQ) and limit of detection (LOD) for the solid-phase microextraction (SPME) based on stearic acid-coated magnetic nanoparticles-BT-HGAAS (SACMNP-BT-HGAAS) method were obtained as 270.8 ng/L and 81.7 ng/L, respectively. The matrix-matching calibration method was performed in order to improve the accuracy of cadmium quantification in tap water and the recovery results obtained were as follows: 88.56 ± 8.92 and 97.43 ± 9.76, for 6.0 and 8.0 ng/mL of cadmium-spiked tap water samples, respectively. Graphical abstract ᅟ.

Development of an efficient and sensitive analytical method for the determination of copper at trace levels by slotted quartz tube atomic absorption spectrometry after vortex-assisted dispersive liquid-liquid microextraction in biota and water samples using a novel ligand.

This study describes the determination of trace levels of copper by slotted quartz tube atomic absorption spectrometry after dispersive liquid-liquid microextraction. A ligand synthesized from the reaction of salicylaldehyde and 1-naphthylamine was used to form coordinate copper complex prior to extraction. All parameters that influence the output of complex formation, extraction, and instrumental measurement were optimized to enhance the absorbance signal of copper. Under the optimum conditions, about 104-fold enhancement in sensitivity was recorded over the conventional flame atomic absorption spectrometer, corresponding to a 0.51 ng/mL detection limit. The percent relative standard deviation calculated for the lowest concentration (4.8%) indicated high precision for the experimental procedure. Accuracy and applicability of the optimum method were determined by performing spiked recovery tests on urine, lake water, and mineral water samples. Satisfactory recovery results were obtained between 82.2 and 106.3% at four different concentrations. Matrix matching method was also performed to increase the accuracy of quantification, and the percent recovery calculated for 175 ng/mL was 105.14%.