An optimized preconcentration method using magnetic dispersive solid-phase microextraction with GO-γFe2O3 nanoparticles for the determination of Se in fish samples by FIA-HG-AAS

This work describes the development of an analytical method for the preconcentration of Se in digested fish samples using magnetic nanoparticles of graphene oxide GO-γFe2O3 with detection by hydride generation...

Simultaneous Determination of Iron and Cobalt using Spectrophotometry after Catanionic Mixed Micellar Cloud Point Extraction Procedure

A new preconcentration method which utilises a mixture of cationic and anionic surfactants for separation and spectrophotometric determination of iron and cobalt simultaneously has been developed. The metal ions, iron and cobalt were complexed with thiocyante. The hydrophobic complexes of iron and cobalt were then extracted into catanionic mixed micelles of cetyltrimethylammonium bromide (CTAB) and sodium dodecyl sulphate (SDS). Different parameters like concentration of HCl, concentration of thiocyanate, concentrations of the surfactants (CTAB and SDS), equilibration temperature and time were studied to get maximum efficiency. The linear ranges of Fe3+ and Co2+ were found to be 0.139 – 0.838 μg mL–1 and 5.89 – 35.4 μg mL–1, respectively the detection limits obtained were 1.54 ng mL–1 and 6.18 ng mL–1. The developed procedure has been employed for the retrieval of Fe3+ and Co2+ in water samples successfully (tap water and sea water). 98 – 107% recoveries were obtained.

Cyclic on-chip bacteria separation and preconcentration

Nanoparticles and biological molecules high throughput robust separation is of significant interest in many healthcare and nanoscience industrial applications. In this work, we report an on-chip automatic efficient separation and preconcentration method of dissimilar sized particles within a microfluidic platform using integrated membrane valves controlled microfiltration. Micro-sized E. coli bacteria are sorted from nanoparticles and preconcentrated on a microfluidic chip with six integrated pneumatic valves (sub-100 nL dead volume) using hydrophilic PVDF filter with 0.45 μm pore diameter. The proposed on-chip automatic sorting sequence includes a sample filtration, dead volume washout and retentate backflush in reverse flow. We showed that pulse backflush mode and volume control can dramatically increase microparticles sorting and preconcentration efficiency. We demonstrate that at the optimal pulse backflush regime a separation efficiency of E. coli cells up to 81.33% at a separation throughput of 120.45 μL/min can be achieved. A trimmed mode when the backflush volume is twice smaller than the initial sample results in a preconcentration efficiency of E. coli cells up to 121.96% at a throughput of 80.93 μL/min. Finally, we propose a cyclic on-chip preconcentration method which demonstrates E. coli cells preconcentration efficiency of 536% at a throughput of 1.98 μL/min and 294% preconcentration efficiency at a 10.9 μL/min throughput.

Comparative Study of Various Methods for Trace SF6 Measurement Using GC-µECD: Demonstration of Lab-Pressure-Based Drift Correction by Preconcentrator

This study presents a high-precision method, using a preconcentrator–gas chromatograph with microelectron capture detector (GC-μECD), to measure SF6 at ambient levels. Carboxen 1000 was used as an adsorbent for the preconcentrator and exhibited a high adsorption efficiency for N2O and SF6 and low adsorption efficiency for O2. This enabled the selective removal of atmospheric O2 from analytes and improved repeatability of the SF6 peak that followed the O2 peak, in a separation column of activated alumina F1. In addition, the increased sensitivity resulting from preconcentrated SF6 improved the signal-to-noise ratio. This led to better analytical precision in comparison with other measurement methods including the conventional and forecut–backflush (FCBF) methods. The precision-to-drift ratios of the conventional, FCBF, and preconcentration methods were 0.11, 0.10, and 0.03, respectively. Analytical precision of the preconcentration method was 0.08% for 10 consecutive injections; this was the best among the three methods. The long-term drift of the SF6 response was inversely proportional to the laboratory pressure. Based on this finding, room pressure can be used to correct for ECD signal drift, with an uncertainty of 0.14% over a 48-h period, using the preconcentration method. Another advantage of the preconcentration method was the excellent linearity of the SF6 response to a wide range of concentrations, including its ambient concentration.