Nickel hydroxide nanoflower-based dispersive solid-phase extraction of copper from water matrix.

In this work, a dispersive solid-phase extraction method based on Ni(OH)2 nanoflowers (Ni(OH)2-NFs-DSPE) was developed to separate and preconcentrate copper ions from tap water samples for determination by flame atomic absorption spectrometry (FAAS). Ni(OH)2-NFs was synthesized using a homogeneous precipitation technique and used as sorbent for copper preconcentration. X-ray diffraction, scanning electron microscopy, and Fourier-transform infrared spectroscopy were used to characterize the synthesized sorbent. All experimental variables were carefully optimized to achieve a high enhancement factor of 107.5-folds with respect to the detection sensitivity of the conventional FAAS. The proposed method's analytical parameters including LOD, LOQ, and linear range were determined as 1.33 µg/L, 4.42 µg/L, and 3.0-40 µg/L, respectively. To assess the applicability and reliability of the developed method, optimal conditions were applied to tap water samples and satisfactory percent recoveries (94-103%) were obtained for the samples spiked at 20 and 30 µg/L. This validated the accuracy and feasibility of the developed method to real samples. The developed method can be described as a simple, efficient, and rapid analytical approach for the accurate determination of trace copper ions in water samples.

Chromium removal from tannery wastewaters with a strong cation exchange resin and species analysis of chromium by MINEQL+ .

Chromium (III) salts are highly applied for tanning purpose in tannery industries. The purpose of this study was removal and recovery of chromium(III) from tannery wastewater with a strong cation exchange resin. For this purpose, Amberlite 252 ZU was chosen as a strong cation exchange resin. In the first part of this study, The MINEQL+ computer program was applied depending on the optimum concentration and pH for determining Cr species in aqueous solutions. The second part of the work consists of measuring the exchange equilibrium of H+ ions and Cr(III) ions. Therefore, solutions containing fixed amounts of chromium were brought into contact with different amounts of resins. The evaluation of the obtained equilibrium parameters was done by surface complexing theory. Retention and regeneration steps were successfully performed in the column without any significant change up to 10 cycles. Efficiency was between 90 and 98% in removal studies, and between 81 and 92% in recovery studies. The results showed that a strong cation exchange resin Amberlite 252 ZU can be successfully used for chromium removal and recovery.

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.