Heavy metals (Cd, Cu, Ni and Pb) content in two fish species of Persian Gulf in Bushehr Port, Iran

Heavy metal (HMs) pollution of aquatic environment has become a great concern in recent years. In this study, cadmium (Cd), copper (Cu), nickel (Ni) and lead (Pb) levels were determined in muscle and skin of two important consumed fishes (Indo-Pacific king mackerel and Tigertooth croaker) in Bushehr Province in the Southwestern of Iran. Heavy metal concentrations were analyzed by using inductively coupled plasma (ICP). The mean contents of metal, expressed in mg/kg wet weight, varied from 0.17 to 0.26 for Cd, 1.25 to 1.84 for Cu, 0.6 to 0.84 for Ni and 0.31 to 0.7 for Pb. Results showed that the highest and lowest contents of heavy metals in muscle and skin of both fish samples were related to Cu and Cd concentration, respectively, and heavy metal contents in both skin fish samples and muscle of Tigertooth croaker were found to decrease in sequence as Cu>Pb>Ni>Cd.Key words: Heavy metal, fish, Bushehr, Iran

Determination of heavy metal content of processed fruit products from Tehran's market using ICP- OES: A risk assessment study

Abstract In this study, the levels of Cd, Hg, Sn, Al, Pb and As of 72 samples (36 samples for fruits juices and 36 samples for fruits canned) of three different brands including of Peach, Orange, Cherry, and Pineapple (18 samples of each fruits) marketed in Tehran, Iran (2015) were evaluated using Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) technique. Also, Probabilistic risk assessment (non-carcinogenic and carcinogenic risks) was estimated by models include target hazard quotient (THQ) and cancer risk (CR) in the Monte Carlo Simulation (MCS) model. However, all samples were contaminated with the heavy metals investigated, most of them not surpassed established standards. The range of concentration for Al, Sn, As, Cd, Hg, and Pb as average in fruit juices were reported as 340.62 (65.17–1039.2), 72.33 (49.76–119.4), 3.76 (1.137–18.36), 2.12 (0.89–3.44), 0.351 and 40.86 (27.87–66.1) μg/kg, respectively. The level of heavy metals measured in different kinds of fruit juices was ranked as Al > Sn > Pb > As > Cd > Hg, and for fruits canned this rank was Pb > Al > Sn > As > Cd > Hg. The range of concentration for Al, Sn, As, Cd, Hg, and Pb in fruits canned were reported as 361.23 (43.15–1121.2), 101.42 (71.45–141.61), 3.92 (1.279–19.50), 2.78 (1.09–5.56), 0.35 and 690.54 (470.56–910.14) μg/kg, respectively. The lead (Pb) concentration in 97.22% (35 out of 36 samples) of fruit juices samples surpassed Codex limit (0.05 mg/kg) and in all samples of FC was lower than the legal limit of Codex limit (1 mg/kg). All of the samples had Tin (Sn) lower than the legal limit of Codex (fruit juices 100 mg/kg and FC 250 mg/kg). The MCS indicated that the rank order of heavy metals in both adults and children based on THQ was Al > Sn > As > Pb > Cd > Hg. The THQ of Al and Sn in the FJ and FC, for both adults, and children, was considerably higher than 1 value. Also, CR of As in both adults and children were higher than 1E-6 value. Although the mean concentration of heavy metal in the FJ and FC was lower than the standard limit, the MCS indicated that adults and children are at considerable non-carcinogenic and carcinogenic risks. Keywords: Heavy metals Fruits juice Health risk assessment Monte Carlo simulation Fruit canned Food safety ICPOES

Multi-walled carbon nanotubes modified with iron oxide and silver nanoparticles (MWCNT-Fe<inf>3</inf>O<inf>4</inf>/Ag) as a novel adsorbent for determining PAEs in carbonated soft drinks using magnetic SPE-GC/MS method

The synthesis of compounds with an excellent adsorption capability plays an essential role to remove contaminants such as phthalic acid esters (PAEs) with potential carcinogenic characteristics from different food products. In this context, for the first time, a novel adsorbent (MWCNT-Fe3O4/Ag) was synthesized by using iron (magnetic agent), and silver (catalytic and surface enhancer agent) to further approach in a magnetic SPE-GC/MS method for determining of PAEs in carbonated soft drink samples. The limit of detection (LOD) and limit of quantification (LOQ) values of MSPE-GC/MS were determined in six PAEs as a range of 10.8–22.5 and 36–75 ng/L, respectively. Also, the calibration curves of PAEs were linear (R2 = 0.9981–0.9995) over the concentration level of 10.000 ng/L and the recoveries of the six PAEs were ranging from 96.60% to 109.22% with the RSDs less than 8%. Moreover, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD), vibrating sample magnetometry (VSM) and transmission electron microscopy analyses (TEM) were utilized to characterize the produced MWCNT-Fe3O4/Ag. Based on the findings, the surface of MWCNT is relatively uniform, which became coarser after loading with Fe3O4/Ag particles. Also, EDX spectrum showed the carbon (C), iron (Fe), oxygen (O), Ag and copper (Cu) are the main components of synthesized MWCNTs-Fe3O4/Ag. The successful adhesion of Fe3O4/Ag on the texture of MWCNTs using a co-precipitation method was confirmed by XRD and FT-IR assays. Additionally, excellent crystallinity and clear lattice nanocrystals fringes of prepared MWCNT-Fe3O4/Ag was demonstrated by TEM analysis. Based on the obtained VSM images, the prepared sorbent (MWCNT-Fe3O4/Ag) has the good magnetic performance for magnetic separation and extraction processes. It was concluded that the synthesized MWCNT-Fe3O4/Ag could be used as an efficient adsorbent for determining contaminants such as PAEs in different beverage samples. © 201

TVOCs and BTEX concentrations in the air of south pars special economic energy zone

cold season were higher than those in warm season. High concentrations of Benzene in cold and warm seasons were used to identify areas of high exposure risk.survey TVOCs and BTEX in the air of South Pars Special Economic Energy Zone in 2014. Materials and methods: In a cross-sectional study sampling and analysis was done by NIOSH 1501 method. The study was carried out in 336 activated carbon tubes and personal sampling pump in 6 sampling stations during one year. The compounds were extracted by solvent carbon disulfide and analyzed using Gas Chromatography- Flame Ionization Detector (GC-FID). Data analysis was performed in SPSS Ver.18 applying Kruskal-Wallis, Fligner test and ANOVA. Results: The mean concentrations of TVOCs and TBTEX were 229.34 and 31.23 µg/m3 in cold season and 212.19 and 29.89 µg/m3 in warm season, respectively. The mean concentrations of Benzene in all stations were 11.72 µg/m3 which were higher than the threshold levels recommended by Iranian Clean Air Act and US Environmental Protection Agency (USEPA). The ANOVA results showed a significant difference between the concentration of pollutants and hour, month and sampling stations (P&lt;0.05), but no significant difference was found between the concentration of pollutants and seasons (P&gt;0.05). Conclusion: The concentrations of measured pollutants in cold season were higher than those in warm season. High concentrations of Benzene in cold and warm seasons were used to identify areas of high exposure risk. © 2016, AMazandaran University of Medical Sciences. All rights reserved

Multi-walled carbon nanotubes modified with iron oxide and silver nanoparticles (MWCNT-Fe 3 O 4 /Ag) as a novel adsorbent for determining PAEs in carbonated soft drinks using magnetic SPE-GC/MS method

The synthesis of compounds with an excellent adsorption capability plays an essential role to remove contaminants such as phthalic acid esters (PAEs) with potential carcinogenic characteristics from different food products. In this context, for the first time, a novel adsorbent (MWCNT-Fe 3 O 4 /Ag) was synthesized by using iron (magnetic agent), and silver (catalytic and surface enhancer agent) to further approach in a magnetic SPE-GC/MS method for determining of PAEs in carbonated soft drink samples. The limit of detection (LOD) and limit of quantification (LOQ) values of MSPE-GC/MS were determined in six PAEs as a range of 10.8�22.5 and 36�75 ng/L, respectively. Also, the calibration curves of PAEs were linear (R 2 = 0.9981�0.9995) over the concentration level of 10.000 ng/L and the recoveries of the six PAEs were ranging from 96.60 to 109.22 with the RSDs less than 8. Moreover, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD), vibrating sample magnetometry (VSM) and transmission electron microscopy analyses (TEM) were utilized to characterize the produced MWCNT-Fe 3 O 4 /Ag. Based on the findings, the surface of MWCNT is relatively uniform, which became coarser after loading with Fe 3 O 4 /Ag particles. Also, EDX spectrum showed the carbon (C), iron (Fe), oxygen (O), Ag and copper (Cu) are the main components of synthesized MWCNTs-Fe 3 O 4 /Ag. The successful adhesion of Fe 3 O 4 /Ag on the texture of MWCNTs using a co-precipitation method was confirmed by XRD and FT-IR assays. Additionally, excellent crystallinity and clear lattice nanocrystals fringes of prepared MWCNT-Fe 3 O 4 /Ag was demonstrated by TEM analysis. Based on the obtained VSM images, the prepared sorbent (MWCNT-Fe 3 O 4 /Ag) has the good magnetic performance for magnetic separation and extraction processes. It was concluded that the synthesized MWCNT-Fe 3 O 4 /Ag could be used as an efficient adsorbent for determining contaminants such as PAEs in different beverage samples. © 2018 The Author

Multi-walled carbon nanotubes modified with iron oxide and silver nanoparticles (MWCNT-Fe3O4/Ag) as a novel adsorbent for determining PAEs in carbonated soft drinks using magnetic SPE-GC/MS method

The synthesis of compounds with an excellent adsorption capability plays an essential role to remove contaminants such as phthalic acid esters (PAEs) with potential carcinogenic characteristics from different food products. In this context, for the first time, a novel adsorbent (MWCNT-Fe3O4/Ag) was synthesized by using iron (magnetic agent), and silver (catalytic and surface enhancer agent) to further approach in a magnetic SPE-GC/MS method for determining of PAEs in carbonated soft drink samples. The limit of detection (LOD) and limit of quantification (LOQ) values of MSPE-GC/MS were determined in six PAEs as a range of 10.8�22.5 and 36�75 ng/L, respectively. Also, the calibration curves of PAEs were linear (R2 = 0.9981�0.9995) over the concentration level of 10.000 ng/L and the recoveries of the six PAEs were ranging from 96.60 to 109.22 with the RSDs less than 8. Moreover, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD), vibrating sample magnetometry (VSM) and transmission electron microscopy analyses (TEM) were utilized to characterize the produced MWCNT-Fe3O4/Ag. Based on the findings, the surface of MWCNT is relatively uniform, which became coarser after loading with Fe3O4/Ag particles. Also, EDX spectrum showed the carbon (C), iron (Fe), oxygen (O), Ag and copper (Cu) are the main components of synthesized MWCNTs-Fe3O4/Ag. The successful adhesion of Fe3O4/Ag on the texture of MWCNTs using a co-precipitation method was confirmed by XRD and FT-IR assays. Additionally, excellent crystallinity and clear lattice nanocrystals fringes of prepared MWCNT-Fe3O4/Ag was demonstrated by TEM analysis. Based on the obtained VSM images, the prepared sorbent (MWCNT-Fe3O4/Ag) has the good magnetic performance for magnetic separation and extraction processes. It was concluded that the synthesized MWCNT-Fe3O4/Ag could be used as an efficient adsorbent for determining contaminants such as PAEs in different beverage samples. © 201

Removal of TPHs from Soil Media using Persulfate Oxidant in the Presence of Mineral Siderite

The objective of the present study was to evaluate the potential of persulfate (PS) oxidant in the presence of mineral siderite (SI) for remediation of fuel oil contaminated soils. Clay and sandy soils were selected as representative soils which were spiked with 5000 mg fuel oil per kilogram of dry' soil. The efleets of controlling factors such as different persulfate concentrations (100-500 mM), siderite concentrations (0.1-0.5 g), pH (3-9), and temperature (20-60 degrees C) were also investigated. The results indicated that in clay and sandy soil samples, the highest total petroleum hydrocarbon (TPHs) degradation was observed in the following condition: pH= 3, soils temperature =60 degrees C and PS/Fe (II) molar ratio = 400 mM/0.4 g and 300 mM/0.3 g in clay and sandy soil, respectively. Based on our findings, using persulfate oxidation in the presence of siderite as an activator is a promising technique to remediate soil contaminated by petroleum hydrocarbons

Efficiency Of Domestic Reverse Osmosis In Removal Of Trihalomethanes From Drinking Water

The reaction of disinfectants with natural organic matters existing in water lead to the formation of Disinfection By-Products. Potentially hazardous and carcinogenic characteristics of trihalomethanes (THMs) are recognized. Thus removal of THMs or its precursors are necessary for human health. The aim of this study was to study the efficiency of domestic reverse osmosis (RO) in removal of trihalomethanes from drinking water. A pilot scale of RO system with Polyamide membrane as Spiral-Wound, Tape wrapping module was used. Feed solution was made by using of pure chloroform. The samples containing chloroform were analyzed using a gas chromatograph equipped with a flame ionization detector. By increasing the flow, the removal rate of chloroform decreased and with declining removal of EC, the removal of chloroform declined too. In this research, at the worst condition, the efficiency of the pilot scale reverse osmosis reached to 80 % removal of chloroform

Source apportionment of BTEX compounds in Tehran, Iran using UNMIX receptor model

Understanding the distribution levels and sources of volatile organic compounds (VOC), mainly benzene, toluene, ethylbenzene and xylenes (BTEX), in the ambient atmosphere is important for efficiently managing and implementing the associated control strategies. We measured BTEX compounds at an industrial location in the west Tehran city (Iran), which is highly influenced by industrial activities and traffic during the winter and spring seasons during 2014-2015. A multivariate receptor model, UNMIX, was applied on the measured data for the identification of the sources and their contributions to BTEX compounds in a highly industrialised and trafficked atmospheric environment of Tehran city. Three main groups of sources were identified. These included solvent and painting sources (e.g. vehicle manufacturing), motorised road vehicles and mixed origin sources. While the solvent and painting sources and vehicle exhaust emissions contributed to about 5 and 29% of total BTEX mass, respectively, the mixed origin source contributed to about two-third (~66%) of the remaining mass. These mixed origin sources included rubber and plastic manufacturing (39%), leather industries (28%) and the unknown sources (33%). The mean concentrations of benzene, toluene, ethylbenzene and average xylene(o, p,m) compounds were measured as 28.96±9.12 µg m –3 , 29.55±9.73 µg m –3 , 28.61±12.2 µg/m-3 and 25.68±10.58 µg m–3 , respectively. A high correlation coefficient (R 2 >0.94) was also found between predicted (modelled) and measured concentrations for each sample. Further analyses from UNMIX receptor model showed that the average weekday contributions of BTEX compounds were significantly higher during winter compared with those during spring. This higher concentration during winter may be attributed to calm wind conditions and high stability of the atmosphere, along with the after effect of government policies on the use of cleaner fuel in refineries that became operational in winter 201