scholarly journals Magnetic Solid Phase Extraction of Au(III) using Fe3O4 Nanoparticles Prior to its Flame Atomic Absorption Spectrometric Determination

2017 ◽  
Vol 6 (2) ◽  
pp. 990-998 ◽  
Author(s):  
Zahra Monsef Khoshhesab
Keyword(s):  
Solid Phase Extraction ◽  
Atomic Absorption ◽  
Solid Phase ◽  
Extraction Procedure ◽  
Maximum Adsorption Capacity ◽  
Phase Extraction ◽  
Flame Atomic Absorption ◽  
Relative Standard ◽  
Separation And Preconcentration

A simple solid phase extraction procedure has been proposed for determination of Au(III) based on separation and preconcentration using magnetite nanoparticles (MNPs) prior to its determination by flame atomic absorption spectrometry. The influences of experimental parameters including sample pH, sorbent mass, contact time, volume and type of eluent, and interference of some ions with extraction of Au(III) ions were investigated using batch procedure. The maximum adsorption capacity of the sorbent for Au(III) was found to be 45.0 mg g-1. The sorption of Au(III) ions was quantitative in the pH range of 4.0–5.0 and quantitative desorption was achieved using 10 mL of thiourea (0.5 mol L-1)/hydrochloric acid (1 mol L-1) solution. In the initial solution, the calibration curve was linear in the range of 8.8 - 666.0 μg L-1 with R2 = 0.9994 (n = 8), the detection limit (3Sb, n = 8) was 6.2 μg L-1, relative standard deviation (R.S.D) of 20 μg mL-1 of Au(III) was 3.9% (n = 8), and the preconcentration factor was 30. The proposed method has been applied to the determination of Au(III) in water and wastewater samples with good recoveries in the range of 95% –103%.

scholarly journals Flame atomic absorption spectrometric determination of trace amounts of lead, cadmium and nickel in different matrixes after solid phase extraction on modified multiwalled carbon nanotubes

2010 ◽  
Vol 8 (3) ◽  
pp. 662-668 ◽  
Author(s):  
S. Mohammadi ◽  
D. Afzali ◽  
D. Pourtalebi
Keyword(s):  
Carbon Nanotubes ◽  
Solid Phase Extraction ◽  
Multiwalled Carbon Nanotubes ◽  
Solid Phase ◽  
Phase Extraction ◽  
Multiwalled Carbon ◽  
Flame Atomic Absorption ◽  
Relative Standard ◽  
Separation And Preconcentration

AbstractThe potential of modified multiwalled carbon nanotubes (a solid-phase extraction sorbent), for the simultaneous separation and preconcentration of lead, cadmium and nickel; has been investigated. Lead, cadmium and nickel, were adsorbed quantitatively; on modified multiwalled carbon nanotubes (in the pH range of 2–4). Parameters influencing, the simultaneous preconcentration of Pb(II), Ni(II) and Cd(II) ions (such as pH of the sample, sample and eluent flow rate, type and volume of elution solution and interfering ions), have been examined and optimized. Under the optimum experimental conditions, the detection limits of this method. for Pb(II), Ni(II) and Cd(II) ions, were 0.32, 0.17 and 0.04 ng mL−1 in original solution, respectively. Seven replicate determinations, of a mixture of 2.0 μg mL−1 lead and nickel, and 1.0 μg mL−1 cadmium; gave a mean absorbance of 0.074, 0.151 and 0.310, with relative standard deviation 1.7%, 1.5% and 1.2%, respectively. The method has been applied, to the determination of trace amounts of lead, cadmium and nickel; in biological and water samples, with satisfactory results.

Green Dispersive Micro Solid-Phase Extraction using Multiwalled Carbon Nanotubes for Preconcentration and Determination of Cadmium and Lead in Food, Water, and Tobacco Samples

2020 ◽  
Vol 16 (4) ◽  
pp. 381-392
Author(s):  
Ayman A. Gouda ◽  
Ali H. Amin ◽  
Ibrahim S. Ali ◽  
Zakia Al Malah
Keyword(s):  
Carbon Nanotubes ◽  
Solid Phase Extraction ◽  
Multiwalled Carbon Nanotubes ◽  
Solid Phase ◽  
Certified Reference Materials ◽  
Phase Extraction ◽  
Multiwalled Carbon ◽  
Flame Atomic Absorption ◽  
Relative Standard ◽  
Separation And Preconcentration

Background: Cadmium (Cd2+) and lead (Pb2+) have acute and chronic effects on humans and other living organisms. In the present work, new, green and accurate dispersive micro solid-phase extraction (DμSPE) method for the separation and preconcentration of trace amounts of cadmium (Cd2+) and lead (Pb2+) ions in various food, water and tobacco samples collected from Saudi Arabia prior to its Flame Atomic Absorption Spectrometric (FAAS) determinations was developed. Methods: The proposed method was based on a combination of oxidized multiwalled carbon nanotubes (O-MWCNTs) with a new chelating agent 5-benzyl-4-[4-methoxybenzylideneamino)-4H- 1,2,4-triazole-3-thiol (BMBATT) to enrich and separate trace levels of Cd2+ and Pb2+. The effect of separation parameters was investigated. The validation of the proposed preconcentration procedure was performed using certified reference materials. Results: Analyte recovery values ranged from 95-102%, indicating that the method is highly accurate. Furthermore, precision was demonstrated by the relative standard deviation (RSD < 3.0%). The limits of detection were 0.08 and 0.1 μg L−1 for Cd2+ and Pb2+ ions, respectively. The preconcentration factor was 200. Conclusion: The proposed method was used for the estimation of Cd2+ and Pb2+ ion content in various real samples, and satisfactory results were obtained. The proposed method has high adsorption capacity, rapid adsorption equilibrium, extremely low LODs, high preconcentration factors and shortens the time of sample preparation in comparison to classical SPE.

scholarly journals Spectrophotometric Determination of Iron(II) after Solid Phase Extraction of Its 2,2′ Bipyridine Complex on Silica Gel-Polyethylene Glycol

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Nahid Pourreza ◽  
Saadat Rastegarzadeh ◽  
Ali Reza Kiasat ◽  
Hossein Yahyavi
Keyword(s):  
Polyethylene Glycol ◽  
Solid Phase Extraction ◽  
Silica Gel ◽  
Limit Of Detection ◽  
Solid Phase ◽  
Extraction Procedure ◽  
Calibration Graph ◽  
Phase Extraction ◽  
Relative Standard

A new solid phase extraction procedure was developed for preconcentration of iron(II) using silica gel-polyethylene glycol (silica-PEG) as an adsorbent. The method is based on retention of iron(II) as 2,2′ bipyridine complex on silica-PEG. The retained complex is eluted by 1.0 mol L−1of sulfuric acid-acetone mixture (1:2) and its absorbance is measured at 518 nm, spectrophotometrically. The effects of different parameters such as pH, concentration of the reagent, eluting reagent, sample volume, amount of adsorbent, and interfering ions were investigated. The calibration graph was linear in the range of 1–60 ng mL−1of iron(II). The limit of detection based on3Sbwas 0.57 ng mL−1and relative standard deviations (R.S.D) for ten replicate measurements of 12 and 42 ng mL−1of iron(II) were 2.4 and 1.7%, respectively. The method was applied to the determination of of iron(II) in water, multivitamin tablet, and spinach samples.

scholarly journals Determination of Low Levels of Lead in Beer Using Solid-Phase Extraction and Detection by Flame Atomic Absorption Spectrometry

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Vanessa N. Alves ◽  
Simone S. O. Borges ◽  
Waldomiro B. Neto ◽  
Nívia M. M. Coelho
Keyword(s):  
Solid Phase Extraction ◽  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Flow Rate ◽  
Flame Atomic Absorption Spectrometry ◽  
Solid Phase ◽  
Absorption Spectrometry ◽  
Phase Extraction ◽  
Flame Atomic Absorption

In this study, a method for the determination of low concentrations of lead in beer samples using solid-phase extraction with a flow injection analysis system and detection by flame atomic absorption spectrometry (FAAS) was developed.Moringa oleiferaseeds were used as a biosorbent material. Chemical and flow variables of the online preconcentration system, such as sample pH, preconcentration flow rate, eluent flow rate, eluent concentration, particle size, and sorbent mass, were studied. The optimum extraction conditions were obtained using a sample pH of 6.0, sample flow rate of 6.0 mL min−1, 63.0 mg of sorbent mass, and 2.0 mol L−1HNO3at a flow rate of 2.0 mL min−1as the eluent. With the optimized conditions, the preconcentration factor, precision, detection limit, consumption index, and sample throughput were estimated as 93, 0.3% (10.0 μg L−1,n=7), 7.5 μg L−1, 0.11 mL, and 23 samples per hour, respectively. The method developed was successfully applied to beer samples and recovery tests, with recovery ranging from 80% to 100%.

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