scholarly journals Evaluation and determination of occupational and environmental exposure of lead in workplace air and human workers based dispersive ionic liquid solid phase micro extraction in battery manufacturing factories from Iran

2021 ◽  
Vol 4 (02) ◽  
pp. 47-59
Author(s):  
Somayeh Mirza Mirza ◽  
Azadeh Yahya Meymandi

The exposure of lead in workplace air and human workers of battery manufacturing factory was evaluated determined by nanotechnology since 2019-2020. Human whole blood (HWB) for subject and healthy peoples (25-55, Men, 40 N) and workplace air (40N) was prepared based on NIOSH sampling. 10 mL of HWB samples added to 20 mg of mixture ionic liquid/ ligand ([HMIM][PF6]/APDC) modified on graphene oxide nanostructures(GONs) at pH=6. After sonication, the lead ions separated/extracted by dispersive ionic liquid solid phase micro extraction (DIL-SPME) and determined by flame atomic absorption spectrometry (F-AAS). All air samples in workplace were analyzed based on NIOSH process. The results showed us the negative correlation between Pb concentration in human blood subject and healthy peoples (r=0.24). The range concentrations of lead in human subject, healthy peoples and workplace air were obtained 193.4-543.7 µg L-1, 85.6-175.9 µgL-1 and 44.7-81.5 µgm-3, respectively. The LOD, linear rang, enrichment factor(EF) and RSD% were achieved 1.25 µg L-1, 5.0- 310 µg L-1, 19.6 and less than 5% by procedure. The method was validated by standard reference material (SRM), the electrothermal atomic absorption spectrometry (ET-AAS) and ICP-MS analyzer for human samples.

2017 ◽  
Vol 82 (5) ◽  
pp. 551-565 ◽  
Author(s):  
Atefeh Nasrollahpour ◽  
Seyyed Moradi ◽  
Seyyed Moradi

A new dispersive solid phase micro-extraction (dispersive-SPME) method for separation and preconcentration of mercury(II) using ionic liquid modified magnetic reduced graphene oxide (IL-MrGO) nanoparticles, prior to the measurement by cold vapour atomic absorption spectrometry (CV-AAS) has been developed. The IL-MrGO composite was characterized by Brunauer? Emmett?Teller method (BET) for adsorption-desorption measurement, thermogravimetric analysis (TGA), powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The method is based on the sorption of mercury( II) on IL-MrGO nanoparticles due to electrostatic interaction and complex formation of ionic liquid part of IL-MrGO with mercury(II). The effect of experimental parameters for preconcentration of mercury(II), such as solution type, concentration and volume of the eluent, pH, time of the sorption and desorption, amount of the sorbent and coexisting ion concentration have been optimized. Under the optimized conditions, a linear response was obtained in the concentration range of 0.08?10 ng mL-1 with a determination coefficient of 0.9995. The limit of detection (LOD) of the method at a signal to noise ratio of 3 was 0.01 ng mL-1. Intra-day and inter-day precisions were obtained equal to 3.4 and 4.5 %, respectively. The dispersive solid phase micro-extraction of mercury(II) on IL-MrGO nanoparticles coupled with cold vapour atomic absorption spectrometry was successfully used for extraction and determination of mercury(II) in water and vegetable samples.


2010 ◽  
Vol 8 (3) ◽  
pp. 617-625 ◽  
Author(s):  
Hossein Abdolmohammad-Zadeh ◽  
Elnaz Ebrahimzadeh

AbstractA rapid dispersive liquid-liquid micro-extraction (DLLME) methodology based on the application of 1-hexylpyridinium hexafluorophosphate [C6py][PF6] ionic liquid (IL) as an extractant solvent was applied for the pre-concentration of trace levels of cobalt prior to determination by flame atomic absorption spectrometry (FAAS). 1-Phenyl-3-methyl-4-benzoyl-5-pyrazolone (PMBP) was employed as a chelator forming a Co-PMBP complex to extract cobalt ions from aqueous solution into the fine droplets of [C6py][PF6]. Some effective factors that influence the micro-extraction efficiency include the pH, the PMBP concentration, the amount of ionic liquid, the ionic strength, the temperature and the centrifugation time which were investigated and optimized. In the optimum experimental conditions, the limit of detection (3s) and the enrichment factor were 0.70 µg L−1 and 60, respectively. The relative standard deviation (RSD) for six replicate determinations of 50 µg L−1 Co was 2.36%. The calibration graph using the pre-concentration system was linear at levels 2–166 µg L−1 with a correlation coefficient of 0.9982. The applicability of the proposed method was evaluated by the determination of trace amounts of cobalt in several water samples.


2007 ◽  
Vol 72 (6) ◽  
pp. 585-590 ◽  
Author(s):  
Morteza Talebi ◽  
Homeyra Safigholi

Arapid, simple, and sensitive procedure based on modified solid phase extraction was developed for the pre-concentration and determination of trace amount of lead in water resources. Lead was reacted with ammonium pyrrolidinedithiocarbamate (APDC) to make a complex. The complex was then collected in a column packed with surfactant-coated alumina. The parameters affecting the collection efficiency and desorption rate of the lead complexes from the column were investigated and optimized. The collection efficiency of the lead complex on the adsorbent was excellent under the optimized conditions. The results obtained from the recovery test showed the capability and reliability of the method for the analysis of trace amounts of lead. The proposed pre-concentration procedure made it possible to apply conventional flame atomic absorption spectrometry (FAAS) for the sensitive determination of trace amounts of lead in water resources. .


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