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In-tube solid-phase microextraction with a hybrid monolithic column for the preconcentration of ultra-trace metals prior to simultaneous determination by ICP-MS. | LitMetric

In-tube solid-phase microextraction with a hybrid monolithic column for the preconcentration of ultra-trace metals prior to simultaneous determination by ICP-MS.

Mikrochim Acta

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry & Chemical Engineering and Center of Materials Analysis, Nanjing University, 163 Xianlin Avenue, Nanjing, 210023, China.

Published: May 2020

AI Article Synopsis

  • This study describes the creation of an amino-functionalized hybrid monolithic column using a one-step method that combines two compounds, which is then utilized in solid-phase microextraction (SPME) to analyze trace metals like Cu(II), Zn(II), Au(III), and Pb(II) using ICP-MS.!* -
  • The developed SPME matrix efficiently retains the target metal ions, showcasing significant adsorption capacities, and allows for their quantitative elution using a specific chemical solution, demonstrating strong detection capabilities with low limits of quantitation and detection.!* -
  • The method's validation with various certified reference materials confirms its accuracy and reliability, particularly in complex samples, making it an effective approach for determining ultra-tr

Article Abstract

The preparation of an amino-functionalized hybrid monolithic column (TEOS-co-AEAPTES) via one-pot co-condensation of tetraethoxysilane (TEOS) and N-(β-aminoethyl)-γ-aminopropyltriethoxysilane (AEAPTES) in a capillary is descibed. It was used as solid-phase microextraction (SPME) matrix followed by inductively coupled plasma-mass spectrometry (ICP-MS) for determination of trace metals. Under optimum conditions, the amino-functionalized SPME material can simultaneously retain Cu(II), Zn(II), Au(III), and Pb(II) with adsorption capacities of 148, 60, 81, and 64 μg m, respectively. Subsequently, these four metal ions can be quantitatively eluted using 1 mol L HNO containing 1% thiourea. The retention mechanism of Cu(II), Zn(II), Au(III), and Pb(II) on the amino-functionalized hybrid monolith was explained as the combination of electrostatic and coordination interactions. With a 10-fold enrichment factor, the calibration curves were established in the range 0.5-100 μg L with linear correlation coefficients above 0.9943 and the limits of quantitation were 0.05 μg L for four target analytes. The limits of detection were 0.006, 0.012, 0.004, and 0.007 μg L for Cu(II), Zn(II), Au(III), and Pb(II), respectively. The protocol was validated by analyzing Certified Reference Materials including standard sediment, soil, and nickel ore, and the results were in good agreement with their certified values. The relative standard deviations of the method were in the range 0.22-17.6%. The recoveries of the four metal ions in spiked samples were in the range 88.0-113.8%. Compared to direct ICP-MS determination, the proposed in-tube SPME procedure can effectively eliminate the interference from complex matrix, especially from those ores with very high content of main metal to improve the accuracy of analysis. Therefore the method is suitable for the simultaneous determination of ultra-trace Cu(II), Zn(II), Au(III), and Pb(II) in environmental and mineral samples. Graphical abstract The preparation of the TEOS-co-AEAPTES monolithic column and the SPME procedure of Cu(II), Zn(II), Au(III), and Pb(II).

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http://dx.doi.org/10.1007/s00604-020-04329-0DOI Listing

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