A Review: Effects of air, water and land dumpsite on human health and analytical methods for determination of pollutants

Environment pollutants are found here and there in developing countries and these contaminations affect the environment adversely. A few remediation of pollution which includes incineration which is the waste treatment process that involves the combustion of organic substances contained in waste material, the waste handling practices, the recycling resource recovery, the avoidance and reduction methods, the adsorption based on nanotechnology and the bioremediation technology which appears as a cost-effective and environmental friendly approach for cleanup. Recently researches shows that various chemicals (VOCs, BTEX, heavy metals) that might be delivered into the air or water can cause unfriendly health effects which was analyzed based on sample treatments (solid phase extraction: SPE, the liquid-liquid microextraction: LLME, the magnetic solid phase extraction: MSPE) and instruments such as ET-AAS, F-AAS and GC-FID methods. The related weight of disease can be substantial, and interest in research on health effects and intervention in explicit populations and openness circumstances is significant for the development of control systems. Pollution control and determination is thusly a significant segment of disease control, and health experts and analytical chemistry specialists need to foster associations with different areas to recognize and carry out need interventions.

A novel modified fenton-like process for efficient remediation of anthracene-contaminated soils before analysis by ultraviolet–visible spectroscopy

Due to the persistence of polycyclic aromatic hydrocarbons (PAHs) in soil and sediments, and their toxic, mutagenic, and carcinogenic effects, the remediation of PAH-contaminated sites is an important role for environment pollution. In this study, the chemical oxidative remediation of anthracene-contaminated soils was investigated by magnetite nanoparticles (Fe3O4) catalyzed Fenton-like oxidation in the presence of hydrogen peroxide 30% (H2O2) and urea-hydrogen peroxide (UHP) at neutral pH. Urea-hydrogen peroxide (UHP), as a safer oxidizing agent, is used for the first time in the Fenton process. The magnetite nanoparticles improved the production of hydroxyl radicals, and the removal of polycyclic aromatic hydrocarbons (anthracene as a model compound) from the soil samples. The structure of Fe3O4 nanoparticles was characterized by FT-IR, XRD, SEM, and vibrating sample magnetometer (VSM). The removal efficiency of anthracene at an initial concentration 2500 (mg kg-1) was 95% for 2.5 mmol by using hydrogen peroxide and 93% for 0.1 mmol of UHP at the optimum oxidation condition. The anthracene reaction was analyzed by ultraviolet-visible spectroscopy (UV-Vis). The UHP safety and efficiency, neutral pH condition, the limited iron leaching and its easy magnetic separation makes magnetite nanoparticles-UHP a promising catalytic system in remediation of polycyclic aromatic hydrocarbons in contaminated soils.

A fast, low-cost and eco-friendly method for routine determination of Bisphenol-A in landfill leachate employing vortex assisted liquid-liquid extraction

Landfills are sites designed to receive and final disposal of a broad variety of urban solid wastes (USW). The decomposition and biodegradation processes generate a leachate of high complexity and toxicity, containing persistent and recalcitrant contaminants that are not usually monitored. Bisphenol-A (BPA) is a synthetic compound applied mostly on the production of polycarbonate plastics, epoxy resins, and is an endocrine disruptor. The presence of BPA in USW urges the development of feasible analytical methods to support the effluent treatment plants and reduce the risks of contamination. The main goal of this work was to develop an efficient, eco-friendly, fast and simple method for routine analysis of BPA in the leachate from landfill. A vortex assisted liquid-liquid extraction (VALLME) using 1-octanol as solvent was performed. BPA recoveries at spiking levels of 2.5, 6.5 and 12.5 µg L-1 were between 60 to 104% with relative standard deviation (RSD) lower than 26%. The linearity of the method was evaluated and the correlation coefficient was (r) 0.9985. The limit of quantification (LOQ) was 2.5 µg L-1 with a pre-concentration factor of 20. The method has advantages such as low consumption of extraction solvent (150 µL), low cost, easy and fast determination.

Developing a magnetic nanocomposite adsorbent based on carbon quantum dots prepared from Pomegranate peel for the removal of Pb(II) and Cd(II) ions from aqueous solution

Agriculture waste is a good choice for the production of carbon dots owing to its abundance, wide availability, eco-friendly nature. In this study a novel magnetic bioadsorbent based on carbon quantum dots (Fe3O4-PPCQDs) from Pomegranate peel (PP) was used as adsorbent to remove lead (Pb) and cadmium (Cd) from 50 mL of water and wastewater samples by magnetic solid phase extraction (MSPE). After adsorption ions with Fe3O4-PPCQDs at pH=6, the concentration of Pb(II) and Cd (II) ions were determined by flame atomic absorption spectrometry (F-AAS). The manufactured of Fe3O4-PPCQDs and GO nanostructures were structurally characterized by scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR). The quantum dots were optically characterized by UV–Vis spectroscopy. Batch adsorption experiment was conducted to examine the effects of pH, contact time, temperature and initial concentration of Pb(II) and Cd(II) from the water. The preconcentration factor and LOD for Cd and Pb were obtained 50, and (1.3 μg L-1; 15.5 μg L-1), respectively. The equilibrium data of ions sorption were well described by Langmuir and Freundlich model. The R2 values obtained by Langmuir model were higher. The absorption capacity of Fe3O4-PPCQDs for cadmium and lead were obtained 17.92 and 23.75 mg g-1, respectively.

Cobalt separation from water and food samples based on penicillamine ionic liquid and dispersive liquid-liquid microextraction before determination by AT-FAAS

The cobalt compounds have adverse health effect on human and caused damage to the DNA cells, neurological and endocrine systems. Therefore, the separation and determination of cobalt in water and food samples must be considered. In this research, the (2S)-2-amino-3-methyl-3-sulfanylbutanoic acid (penicillamine) as a chelating agent mixed with ionic liquid (OMIM PF6) /acetone and used for extraction of cobalt from 50 mL of water samples by ultra-assisted dispersive liquid-liquid microextraction (USA-DLLME) at pH=6. Based on procedure, the samples were shaked for 5 min (25oC) and after complexation of cobalt ions by thiol and amine group of penicillamine, the ionic liquid phase separated in the bottom of the conical tube by centrifuging for 3.0 min. The upper liquid phase was vacuumed by the auto-sampler and the Co2+ ions back extracted from the ionic liquid/ penicillamine in acidic pH. Finally, the cobalt concentration in remained solution was determined by atom trap flame atomic absorption spectrometry (AT-FAAS). The main parameters such as the sample volume, the penicillamine amount, the ionic liquid amount and the shaking time were optimized. The linear range, the detection limit (LOD) and enrichment factor were obtained 1.5-62 μg L-1, 0.38 μg L-1 and 98.5, respectively (r = 0.9995, RSD%=2.2).

Adsorption and determination of Lead in water and human urine samples based on Zn2(BDC)2(DABCO) MOF as polycaprolactone nanocomposite by suspension micro solid phase extraction coupled to UV–VIS spectroscopy

Today, the safety of water resource is the most important challenges which was reported by health and environment organizations. Water pollution can be created by hazardous contaminants of environmental pollutions. Lead as a heavy metal has carcinogenic effects in humans. Metal organic framework (MOF) is a highly porous material with different application. The Zn2(BDC)2(DABCO) is a good candidate of MOF based on zinc metal (Zn-MOF) with potential adsorption/extraction. In this work, Zn2(BDC)2(DABCO) MOF as polycaprolactone (PCL) nanocomposite were applied for lead adsorption/extraction from 50 mL of aqueous solution by ultra-assisted dispersive suspension-micro-solid phase extraction procedure (USA-S- µ-SPE) at pH=8. The samples were characterized by the FTIR, the XRD analysis, the FE-SEM and the BET surface area. The effect of parameters was investigated on lead absorption before determined by UV–VIS spectroscopy. The linear range, the detection limit (LOD) and enrichment factor of adsorbent were obtained 0.05-1 mg L-1, 0.25 μg L-1 and 48.7, respectively (r = 0.9992, RSD%=3.65). The absorption capacity of Zn2(BDC)2(DABCO) MOF for 50 mg L-1 of standard lead solution were obtained 133.8 mg g-1 for 0.25 g of adsorbent. The results indicate that this nanocomposite can have a good potential to develop different adsorbents.

Thallium extraction in urine and water samples by nanomagnetic 4-Aminothieno[2,3-d] pyrimidine-2-thiol functionalized on graphene oxide

Thallium is a water-soluble metal and extra dosage has toxicological effect in human body. Thallium is readily absorbed by inhalation, ingestion and skin contact. The symptomatology of thallium toxicity was seen in patients with hemorrhage, bone/gastrointestinal problems, delirium, convulsions and coma. So, accurate determination of thallium in water and human urine is necessary. In this research, a novel and applied method based on 25 mg of nanomagnetic 4-Aminothieno[2,3-d] pyrimidine-2-thiol functionalized on graphene oxide (Fe3O4-ATPyHS@GO) was used for thallium extraction in 50 mL of water, wastewater and urine samples by dispersive magnetic micro solid-phase extraction (DM-μ-SPE). After extraction and back-extraction of solid phase by 1 mL of nitric acid solution, the concentration of thallium ions determined by flame atomic absorption spectrometry (F-AAS). The working/linear range, the limit of detection (LOD), and preconcentration factor (PF) were achieved (4-1400 μg L−1; 4-300 μg L−1), 0.9 µg L−1, and 50, respectively (Mean RSD%=1.8 water; 2.1 urine). The absorption capacity of Go and Fe3O4-ATPyHS@GO adsorbent were achieved 7.2 and 137.5 mg g-1 for 5 mg L-1 of thallium, respectively. The procedure was validated by ICP-MS analyzer.

Ionic liquid functionlized on multiwall carbon nanotubes for nickel and lead determination in human serum and urine samples by micro solid-phase extraction

In this study, a novel synthesis adsorbent, 1-(3-aminopropyl)-3-methylimidazolium hexafluorophosphate functionlized on multiwall carbon nanotubes ([Apmim][PF6]-MWCNTs, IL@MWCNTS) was used for nickel/lead (Ni/Pb) extraction and determination by dispersive ionic liquid micro solid-phase extraction (DIL-μ-SPE) coupled to electrothermal atomic absorption spectrometry (ET-AAS). After dilution of 20 mg of IL@MWCNTS in 200 μL of acetone, the mixture was injected to 10 mL of human serum/urine samples at pH of 8.0. After sonication for 5 min, the Ni(II) / Pb(II) were extracted by ionic liquid phase and then centrifuged for 2.5 min. The upper liquid phase set aside and Ni(II) / Pb(II) loaded in adsorbent were back-extracted by acidic solution at pH=2-3. Finally, the concentration of total nickel and lead was determined by ET-AAS. By optimizing, the limit of detection, linear range, and enrichment factor for nickel and lead were obtained (0.05 μg L−1; 0.1 μg L−1), (0.2-5.8 μg L−1; 0.4-30 μg L−1) and 24.7; 5.1, respectively (RSD less than 5%). Also, the capacity absorption of IL@MWCNTS for nickel and lead ions were achieved 149.3 mg g-1 and 162.5 mg g-1, respectively. The DIL-μ-SPE procedure was validated for nickel and lead extraction by spiking of real samples and ICP-MS analyzer.

Determination of fenthion in environmental water samples by dispersive liquid–liquid microextraction coupled with spectrofluorimetric and chemometrics methods

In the present study, a simple, rapid and efficient dispersive liquid–liquid microextraction (DLLME) coupled with spectrofluorimetry and chemometrics methods have been proposed for the preconcentration and determination of fenthion in water samples. Box–Behnken design was applied for multivariate optimization of the extraction conditions (sample pH, the volume of dispersive solvent and volume of extraction solvent). Analysis of variance was performed to study the statistical significance of the variables, their interactions and the model. Under the optimum conditions, the calibration graph was linear in the range of 5.0–110.0 ng mL-1 with the detection limit of 1.23 ng mL-1 (3Sb/m). Parallel factor analysis (PARAFAC) and partial least square (PLS) modelling were applied for the multivariate calibration of the spectrofluorimetric data. The orthogonal signal correction (OSC) was applied for preprocessing of data matrices and the prediction results of model, and the analysis results were statistically compared. The accuracy of the methods, evaluated by the root mean square error of prediction (RMSEP) for fenthion by OSC-PARAFAC and OSC-PLS models were 0.37 and 0.78, respectively. The proposed procedure could be successfully applied for the determination of fenthion in water samples.

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

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.