Magnetic graphitic carbon nitride nano-composite for ultrasound-assisted dispersive micro-solid-phase extraction of Hg(II) prior to quantitation by atomic fluorescence spectroscopy

2019 ◽  
Vol 1074 ◽  
pp. 33-42 ◽  
Author(s):  
Meng-ting Shi ◽  
Xin-an Yang ◽  
Wang-bing Zhang
2013 ◽  
Vol 2013 ◽  
pp. 1-15 ◽  
Author(s):  
Mirna Daye ◽  
Baghdad Ouddane ◽  
Jalal Halwani ◽  
Mariam Hamzeh

8-Hydroxyquinoline (8-HQ) was chosen as a powerful ligand for Hg solid phase extraction. Among several chelating resins based on 8-HQ, 5-phenylazo-8-hydroxyquinoline (5Ph8HQ) is used for mercury extraction in which the adsorption dynamics were fully studied. It has been shown that Hg(II) is totally absorbed by 5Ph8HQ within the first 30 minutes of contact time witht1/25 minutes, following Langmuir adsorption model. At pH 4, the affinity of mercury is unchallenged by other metals except, for Cu(II), which have shown higher Kd value. With these latter characteristics, 5Ph8HQ was examined for the preconcentration of trace levels of Hg(II). The developed method showed quantitative recoveries of Hg(II) with LOD = 0.21 pg mL−1and RSD = 3–6% using cold vapor atomic fluorescence spectroscopy (CV-AFS) with a preconcentration factor greater than 250.


2018 ◽  
Vol 1 (01) ◽  
pp. 47-56 ◽  
Author(s):  
Bahareh Fahimirad ◽  
Alireza Asghari

In this research, a magnetic graphitic carbon nitride (g-C3N4-SnFe2O4) was successfully synthesized and utilized as an efficient adsorbent for nickel (Ni2+) separation/extraction from vegetable samples by ultrasound-assisted magnetic dispersive micro solid-phase extraction (UA-M-D-μSPE). After separation and preconcentration step, Ni ions were determined via micro-sampling flame atomic absorption spectrometry (MS-FAAS). A successful synthesis of g-C3N4-SnFe2O4 was investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and vibrating sample magnetometer (VSM). The optimization of adsorption and desorption steps was effectively studied by the on-at-a time method. In addition, under the optimum experimental conditions, the limits of detection (LODs), the linear ranges (LR) and relative standard deviations (RSDs%, for n = 5) were obtained 1.0 μg.L−1, 4.0 ─ 500.0 μg.L−1, and 1.4 respectively.


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