scholarly journals SOLID PHASE EXTRACTION BASED ON Mn3O4-TIO2 NANOCOMPOSITE FOR THE DETERMINATION OF MOLYBDENUM IN WATER SAMPLES

2021 ◽  
Vol 44 (02) ◽  
Author(s):  
THANH THUY TRAN ◽  
VAN DAT DOAN ◽  
XUAN HUNG NGUYEN ◽  
UYEN TRUONG
Keyword(s):  
Solid Phase Extraction ◽  
Water Samples ◽  
Solid Phase ◽  
Calibration Graph ◽  
Phase Extraction ◽  
Linear Calibration ◽  
Elution Condition ◽  
Relative Standard ◽  
Naoh Solution

The Mn3O4-TiO2 nanocomposite was applied as a new solid phase adsorbent for preconcentration of Molybdenum before determination by an UV-Vis spectrophotometer. The solid-phase extraction conditions as pH, the mass of sorbent, contact time, stirring speed, and the elution condition were investigated. Under optimized conditions, the adsorption capacity of adsorbent was 20.69 mg/g, and the elution condition was 0.2M NaOH solution. Molybdenum ions were determined based on its catalytic effect on the oxidation of 1-amino-2- naphthol-4-sulfonic acid (ANSA) with H2O2. The linear calibration graph was in the range of 0.2–2.5 µg/L (r2 = 0.995) with a detection limit of 0.0502 µg/L. The relative standard deviation for five measurements of 2 µg/L of Mo (VI) was 3,37%. The method was applied to the determination of Molybdenum in water samples.

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.

Eggshell Membrane Biomaterials for Adsorption and Determination of Mn(II, VII) in Environmental Water

2012 ◽  
Vol 457-458 ◽  
pp. 536-539 ◽  
Author(s):  
Rui Hua Zhang ◽  
Xiao Li Yang ◽  
Jin Liu ◽  
Xian Zhong Cheng
Keyword(s):  
Solid Phase Extraction ◽  
Water Samples ◽  
Solid Phase ◽  
Extraction Procedure ◽  
Environmental Water ◽  
Eggshell Membrane ◽  
Environmental Water Samples ◽  
Phase Extraction ◽  
Relative Standard

A simple solid phase extraction procedure for adsorption and preconcentration of manganese(II, VII) in environmental water samples has been proposed prior to inductively coupled plasma mass spectrometry. The procedure presented based on quantitative recoveries of manganese >95%. In this work, the potential use of eggshell membrane(ESM), a typical biomaterial, as solid-phase extraction (SPE) adsorbent is evaluated for analysis of trace manganese. The analytical variables, pH, flow rate, sample volume, elution, coexisting ions for optimum recoveries of manganese (II) and manganese (VII) were investigated. The preconcentration factor was 60. The detection limit (3) of manganese was 0.031 ng L-1. The relative standard deviations of determination was found to be 3.21%. The procedure was successfully applied to the adsorption and determination of manganese in environmental water samples.

Development of a solid-phase extraction – spectrofluorimetric method for trace glutathione determination

2011 ◽  
Vol 89 (4) ◽  
pp. 517-523 ◽  
Author(s):  
Ke-Jing Huang ◽  
Cong-Hui Han ◽  
Ying-Ying Wu ◽  
Chao-Qun Han ◽  
De-Jun Niu ◽  
...  
Keyword(s):  
Solid Phase Extraction ◽  
Limit Of Detection ◽  
Solid Phase ◽  
Signal To Noise Ratio ◽  
Calibration Graph ◽  
Extraction Column ◽  
Phase Extraction ◽  
Selective Reaction ◽  
Spectrofluorimetric Method ◽  
Relative Standard

A simple and efficient solid-phase extraction – spectrofluorimetric method has been developed to determine glutathione (GSH). Fluorescent probe N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-yl)methyl)iodoacetamide (BODIPY Fl-C1-IA) was used as the derivatization reagent. The procedure was based on a BODIPY Fl-C1-IA selective reaction with GSH to form the highly fluorescent product BODIPY Fl-C1-IA–GSH, using a solid-phase extraction column and spectrofluorimetric determination. The variables affecting analytical performance were studied and optimized. The calibration graph using the preconcentration system for GSH was linear over the range of 1–200 nmol/L with a limit of detection of 0.05 nmol/L (signal-to-noise ratio = 3). The relative standard deviation for six replicate determinations of GSH at the 100 nmol/L concentration level was 3.9%. The method was applied to water samples and average recoveries between 87.5% and 111.5% were obtained for spiked samples.

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