Solid Phase Extraction to On-Line Preconcentrate Trace Cadmium Using Chemically Modified Nano-Carbon Black with 3-Mercaptopropyltrimethoxysilane

Carbon black (CB) grafted with 3-mercaptopropyltrimethoxysilane (3-MPTMS) was used as solid phase extractor for Cd2+ in a flow injection system coupled to flame atomic absorption spectrometry (FAAS). The influence of pH, buffer concentration, preconcentration flow rate and eluent concentration on preconcentration of Cd2+ were investigated by means of chemometric tools. The characterization of the adsorbent chemically modified was performed by Fourier transform infrared, scanning electron microscopy, energy dispersive X-ray spectroscopy, thermogravimetric analysis, Raman spectroscopy and textural analysis. To perform the on-line preconcentration, 20.0 mL of a pH 7.0 Cd2+ solution at a flow rate of 4.0 mL min−1 was loaded through 30.0 mg of modified CB and then eluted with 1.0 mol L−1 HCl toward the FAAS instrument. The limits of detection and quantification were found to be 0.20 and 0.66 µg L−1, respectively. Addition and recovery tests carried out in real samples (mineral, tap and saline waters, and cigarette sample) and the analysis of certified reference material (TORT-2, lobster hepatopancreas reference) attested the applicability of proposed method

Solid phase extraction to on-line preconcentrate trace cadmium using chemically modified nano-carbon black with 3-mercaptopropyltrimethoxysilane

Carbon black (CB) grafted with 3-mercaptopropyltrimethoxysilane (3-MPTMS) was used as solid phase extractor for Cd2+ in a flow injection system coupled to flame atomic absorption spectrometry (FAAS). The influence of pH, buffer concentration, preconcentration flow rate and eluent concentration on preconcentration of Cd2+ were investigated by means of chemometric tools. The characterization of the adsorbent chemically modified was performed by Fourier transform infrared, scanning electron microscopy, energy dispersive X-ray spectroscopy, thermogravimetric analysis, Raman spectroscopy and textural analysis. To perform the on-line preconcentration, 20.0 mL of a pH 7.0 Cd2+ solution at a flow rate of 4.0 mL min(-1) was loaded through 30.0 mg of modified CB and then eluted with 1.0 mol L-1 HCl toward the FAAS instrument. The limits of detection and quantification were found to be 0.20 and 0.66 mu g L-1, respectively. Addition and recovery tests carried out in real samples (mineral, tap and saline waters, and cigarette sample) and the analysis of certified reference material (TORT-2, lobster hepatopancreas reference) attested the applicability of proposed method271017151726CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQCOORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPES481669/2013-2; 305552/2013-9; 472670/2012-325/2014Fundacao Araucaria; Laboratorio de Espectroscopia da Central de Multiusuario da Pro-Reitoria de Pesquisa e Pos-Graduacao (PROPPG); Companhia de Saneamento do Parana (SANEPAR); Instituto Nacional de Ciencia e Tecnologia de Bioanalitica (INCT