Abstract Simultaneous adsorption of heavy metals in complex multi metal system is insufficiently explored. This research gives results of key process parameters optimization for simultaneous removal of Cd(II), Co(II), Cr(III), Cu(II), Mn(II), Ni(II) and Pb(II) from aqueous solution (batch system). New lemon peel-based biomaterial was prepared and characterized by infrared spectroscopy with Fourier transformation (FTIR), scanning electron microscopy (SEM), electron dispersive spectroscopy (EDS), while the quantification of metals was made by atomic absorption spectrometry (AAS). Simultaneous removal of seven metals ions was favorable at pH 5 with 300 mg/50 mL solid-liquid phase ratio, within 60 min at room temperature with total obtained adsorption capacity of 46.77 mg g−1. Kinetic modeling showed that pseudo-second order kinetic and Weber-Morris diffusion models best describe the adsorption mechanism of all seven heavy metals onto lemon peel.

Abstract Simultaneous adsorption of heavy metals in complex multi metal system is insufficiently explored. This research gives results of key process parameters optimization for simultaneous removal of Cd(II), Co(II), Cr(III), Cu(II), Mn(II), Ni(II) and Pb(II) from aqueous solution (batch system). New lemon peel-based biomaterial was prepared and characterized by infrared spectroscopy with Fourier transformation (FTIR), scanning electron microscopy (SEM), electron dispersive spectroscopy (EDS), while the quantification of metals was made by atomic absorption spectrometry (AAS). Simultaneous removal of seven metals ions was favorable at pH 5 with 300 mg/50 mL solid-liquid phase ratio, within 60 min at room temperature with total obtained adsorption capacity of 46.77 mg g−1. Kinetic modeling showed that pseudo-second order kinetic and Weber-Morris diffusion models best describe the adsorption mechanism of all seven heavy metals onto lemon peel.

This article reports on an investigation into the ability of SiO2–Ta2O5 as a new sorbent for simultaneous preconcentration of Cd(ii), Co(ii), Cr(iii), Cu(ii), Fe(iii), Mn(ii), Ni(ii) and Pb(ii) ions from water by the column method and the parameters involved in this process.

This article reports on an investigation into the ability of SiO2–Ta2O5 as a new sorbent for simultaneous preconcentration of Cd(ii), Co(ii), Cr(iii), Cu(ii), Fe(iii), Mn(ii), Ni(ii) and Pb(ii) ions from water by the column method and the parameters involved in this process.

Abstract A silica-based inorganic sorbent was synthesized by the thermal decomposition of ammonium heptamolybdate on silica and applied for the preconcentration and simultaneous determination of Cd, Co, Cr, Cu, Fe, Mn, Ni, and Pb in river water samples using a column system with flame atomic absorption spectrometry. Attenuated total reflection-Fourier transformation infrared spectroscopy, scanning electron microscopy, and electron dispersive spectroscopy were used for sorbent characterization. The effects of pH, sample volume, eluent type, eluent concentration, eluent volume, sample flow rate, and matrix ions (Al, Bi, Ca, Mg, and Zn) on the recovery of the metals in model solutions were investigated. The adsorption capacities (µmol g−1) of SiO2-MoO3 were 88.96 (Cd), 169.69 (Co), 153.85 (Cr), 188.88 (Cu), 179.05 (Fe), 163.81 (Mn), 136.31 (Ni), and 38.61 (Pb). The detection limits of the method were 9.09, 10.82, 10.77, 49.57, 31.64, 6.40, 8.86, 19.15 µg L−1 for Cd, Co, Cr, Cu, Fe, Mn, Ni, and Pb, respectively, with a preconcentration factor of 25. The developed method was used for the determination of the target metals in real samples and the recoveries for spiked samples were found to be from 91.2% to 102.9%.

Abstract A silica-based inorganic sorbent was synthesized by the thermal decomposition of ammonium heptamolybdate on silica and applied for the preconcentration and simultaneous determination of Cd, Co, Cr, Cu, Fe, Mn, Ni, and Pb in river water samples using a column system with flame atomic absorption spectrometry. Attenuated total reflection-Fourier transformation infrared spectroscopy, scanning electron microscopy, and electron dispersive spectroscopy were used for sorbent characterization. The effects of pH, sample volume, eluent type, eluent concentration, eluent volume, sample flow rate, and matrix ions (Al, Bi, Ca, Mg, and Zn) on the recovery of the metals in model solutions were investigated. The adsorption capacities (µmol g−1) of SiO2-MoO3 were 88.96 (Cd), 169.69 (Co), 153.85 (Cr), 188.88 (Cu), 179.05 (Fe), 163.81 (Mn), 136.31 (Ni), and 38.61 (Pb). The detection limits of the method were 9.09, 10.82, 10.77, 49.57, 31.64, 6.40, 8.86, 19.15 µg L−1 for Cd, Co, Cr, Cu, Fe, Mn, Ni, and Pb, respectively, with a preconcentration factor of 25. The developed method was used for the determination of the target metals in real samples and the recoveries for spiked samples were found to be from 91.2% to 102.9%.

ABSTRACT The pulverized peel of unmodified and modified pumpkin (Cucurbita pepo L.) was used as sorbent for the determination of Cd, Co, Cr, Fe, Mn, Ni, and Pb by flame atomic absorption spectrometry. The parameters affecting the preconcentration efficiency were investigated. The optimal conditions for preconcentration on unmodified pumpkin peel were identical to those using modified peel: a pH of 8, a preconcentration factor of 10, a flow rate of 3 mL min−1, and an eluent concentration of 1 mol L−1 for all analytes. The detection limits of the method were 9.2, 8.8, 13.2, 28.7, 6.6, 7.6, and 16.5 µ g L−1, while the quantification limits were 30.6, 29.2, 43.9, 95.5, 22.1, 25.4, and 55.1 µ g L−1 for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively. The accuracy of the method was verified with a certified reference material. The relative standard deviation was less than 4% based on 12 measurements. Under the optimum conditions of preconcentration, the recovery values exceeded 94%. The following capacity order was obtained for the analytes (µmol g−1): Ni2+ > Co2+ > Fe3+ > Mn2+ > Cr3+ > Cd2+ > Pb2+.

ABSTRACT The pulverized peel of unmodified and modified pumpkin (Cucurbita pepo L.) was used as sorbent for the determination of Cd, Co, Cr, Fe, Mn, Ni, and Pb by flame atomic absorption spectrometry. The parameters affecting the preconcentration efficiency were investigated. The optimal conditions for preconcentration on unmodified pumpkin peel were identical to those using modified peel: a pH of 8, a preconcentration factor of 10, a flow rate of 3 mL min−1, and an eluent concentration of 1 mol L−1 for all analytes. The detection limits of the method were 9.2, 8.8, 13.2, 28.7, 6.6, 7.6, and 16.5 µ g L−1, while the quantification limits were 30.6, 29.2, 43.9, 95.5, 22.1, 25.4, and 55.1 µ g L−1 for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively. The accuracy of the method was verified with a certified reference material. The relative standard deviation was less than 4% based on 12 measurements. Under the optimum conditions of preconcentration, the recovery values exceeded 94%. The following capacity order was obtained for the analytes (µmol g−1): Ni2+ > Co2+ > Fe3+ > Mn2+ > Cr3+ > Cd2+ > Pb2+.

A procedure for the determination of trace levels of Cd, Co, Cr, Fe, Mn, Ni, and Pb by flame atomic absorption spectrometry using a column preconcentration system is described in which the metals were adsorbed on pulverized banana peel, an economically and environmentally acceptable sorbent. In the optimization procedure, five variables (sample pH, mass of biosorbent, type of eluent, sample flow rate, and volume) were optimized and the capacity of the biosorbent was established. Under the optimized conditions, the detection limits of the method were 2.4, 27.0, 49.4, 31.1, 6.7, 29.6, and 46.2 µg L−1 for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively. The precision, expressed as relative standard deviation, was less than 4% based on twelve measurements. The recoveries were 81.1% (Cd), 91.4% (Co), 87.2% (Cr), 90.1% (Fe), 88.0% (Mn), 94.1% (Ni), and 93.2% (Pb) under the optimum conditions (pH; 9, sample flow rate; 3 mL min−1, mass of biosorbent; 200 mg; eluent; 1 mol L−1 nitric acid, preconcentration factor; 10). The sorption capacity of pulverized banana peel was 15.12, 28.85, 32.70, 30.44, 30.94, 28.97, and 8.21 µmol per gram of adsorbent for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively.

A procedure for the determination of trace levels of Cd, Co, Cr, Fe, Mn, Ni, and Pb by flame atomic absorption spectrometry using a column preconcentration system is described in which the metals were adsorbed on pulverized banana peel, an economically and environmentally acceptable sorbent. In the optimization procedure, five variables (sample pH, mass of biosorbent, type of eluent, sample flow rate, and volume) were optimized and the capacity of the biosorbent was established. Under the optimized conditions, the detection limits of the method were 2.4, 27.0, 49.4, 31.1, 6.7, 29.6, and 46.2 µg L−1 for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively. The precision, expressed as relative standard deviation, was less than 4% based on twelve measurements. The recoveries were 81.1% (Cd), 91.4% (Co), 87.2% (Cr), 90.1% (Fe), 88.0% (Mn), 94.1% (Ni), and 93.2% (Pb) under the optimum conditions (pH; 9, sample flow rate; 3 mL min−1, mass of biosorbent; 200 mg; eluent; 1 mol L−1 nitric acid, preconcentration factor; 10). The sorption capacity of pulverized banana peel was 15.12, 28.85, 32.70, 30.44, 30.94, 28.97, and 8.21 µmol per gram of adsorbent for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively.

A study of the atmospheric particulate size distribution of total suspended particulate matter(TSPM) and associated heavy metals concentrations has been carried out for the urban part of Sarajevo city,Bosnia and Herzegovina. Urban particles (n=150) were collected using a high volume air sampler equippedwith a 6-stage impactor. Apart from Fe which has been determined by flame atomic absorption spectrometry(FAAS), all measurements (Co, Cu, Mn) have been carried out by graphite furnace atomic absorptionspectrometry (GFAAS). The average concentrations of particulate matter are 37%, 18%, 15%, 8%, 15% and6% (averaged over all the observations) of total suspended particulate for PM 7.2, respectively. Metal concentrations in size-fractionated urban particles ranged from 0.01-3.83 ng/m3 for Co, 6.30-179.20 ng/m3 for Cu, 5.00-208.70 ng/m3 for Mn and 0.35-6.82 g/m3 for Fe. Major concentrations of investigated metals are associated with the PM 7.2-3.0 μm. Overall, the decreasing trend of average trace element concentrations (24-h) in the particulates revealed the following order: Fe>Mn>Cu>Co.