Synthesis and characterization of Fe3O4@SiO2 -supported metal-organic framework PAEDTC@MIL-101 (Fe) for degradation of chlorpyrifos and diazinon pesticides.

In this study, a new core-shell Fe3O4@SiO2/PAEDTC@MIL-101 (Fe) photocatalyst was prepared by sol-gel method and used to degrade diazinon (DZN) and chlorpyrifos (CPS) from aqueous solutions. The characteristics analyzed by various techniques indicate that the core-shell photocatalyst with a specific surface area of 992 m2/g, pore size of 1.35 nm and saturation magnetization of nanocomposite was 12 emu/g has been successfully synthesized and can be separated from the reaction solution by a magnetic field. The maximum efficiencies of DZN (98.8%) and CPS (99.9%) were provided at pH of 5, photocatalyst dosage of 0.6 g/L, pollutant concentration of 25 mg/L, radiation intensity of 15 W, and time of 60 min. The presence of anions such as sulfate, nitrate, bicarbonate, phosphate, and chloride had a negative effect on the performance of the photocatalysis system. Compared to the adsorption and photolysis systems alone, the photocatalytic process based on Fe3O4@SiO2/PAEDTC@MIL-101 (Fe) under two UV and visible light sources showed a high efficiency of 90% in the reaction time of 60 min. The BOD5/COD ratio improved after 50 min to above 0.4 with TOC and COD removal rates >80%. Scavenging tests showed that •OH radical, hole (h+), electron (e-), and O2•- anion were produced in the reaction reactor, and the •OH radical was the dominant species in the degradation of DZN and CPS. The stability tests confirmed the recyclability of the photocatalyst in 360 min of reactions, with a minimum reduction of 7%. Energy consumption for the present system during different reactions was between 15.61 and 25.06 kWh/m3 for DZN degradation and 10-22.87 kWh/m3 for CPS degradation.

Application of a novel composite of Fe3O4@SiO2/PAEDTC surrounded by MIL-101(Fe) for photocatalytic degradation of penicillin G under visible light.

The novel photocatalyst of Fe3O4@SiO2/PAEDTC@MIL-101(Fe) was prepared based on the sol-gel method, and its structure and morphology were determined by SEM mapping, TEM, XRD, FTIR, and N2 adsorption-desorption analyses. The photocatalytic activity of nanocomposite was evaluated in comparison with other particles as well as adsorption and photolysis processes. The effect of operating parameters showed that the complete degradation of penicillin G (PNG) can be provided at a photocatalyst dosage of 0.6 g/L, radiation intensity of 36 W, pH of 5, and time of 60 min. In the optimum condition, 84% TOC removal was attained and the BOD5/COD rate for the treated effluent was above 0.4, which was representative of the high biodegradability of the treated effluent compared to the raw sample. The findings of energy consumption showed that PNG can be easily and effectively treated by the photocatalytic process based on magnetic MIL-101(Fe) with electrical energy per order between 10 and 20.87 kWh/m3. Due to the excellent interaction between the MIL-101(Fe) and Fe3O4@SiO2/PAEDTC, the photocatalyst stability test showed a recyclability of the particles for 5 consecutive reaction cycles with a minimum reduction of 7%. Solution treated with photocatalyst under UV and visible light sources explained that the toxicity of the effluent after treatment is significantly reduced with the growth of Escherichia coli. Scavenging experiments showed that •OH radical and hole (h+) are the main agents in degrading PNG to CO2, H2O, and biodegradable and low-toxicity products. Finally, the findings of the diagnostic analysis and comparative experiments proved that with the interaction of Fe3O4@SiO2, NH2, and MIL-101(Fe), a lower band gap can be prepared for more absorption of photons and pollutant and also more and faster production of active radicals.

Photocatalytic degradation of ciprofloxacin by MMT/CuFe2O4 nanocomposite: characteristics, response surface methodology, and toxicity analyses.

The photocatalytic degradation of ciprofloxacin (CIP) was examined by loading spinel ferrite copper (CuFe2O4) nanoparticles onto montmorillonite (MMT) under irradiation using UV light. The laboratory parameters were optimized using response surface methodology (RSM), and maximum efficiency (83.75%) was achieved at a pH of 3, CIP concentration of 32.5 mg/L, MMT/CuFe2O4 dose of 0.78 g/L, and irradiation time of 47.50 min. During the photocatalysis process, the experiments on radical trapping demonstrated the generation of hydroxyls (•OH), superoxide (•O2-) radical, electrons (e-), and holes (h+). A low rate drop (below 10%) in the CIP degradation during the six consecutive reaction cycles corroborated the remarkable recyclability and stability of the MMT/CuFe2O4. The acute toxicity of the treated solution was determined using Daphnia Magna, by applying photocatalysis, which was indicative of a marked decline in the toxicity. Comparing the findings of the degradation using UV and the degradation process using visible light represented results with close resemblance to each other at the end of the reaction time. Besides, under UV and visible light, the particles in reactor are easily activated when the pollutant mineralization exceeded 80%.

The application of a new recyclable photocatalyst γ-Fe2O3@SiO2@ZIF8-Ag in the photocatalytic degradation of amoxicillin in aqueous solutions.

This pilot study synthesized the γ-Fe2O3@SiO2@ZIF8-Ag nanocomposites via the hydrothermal method to study its potential use in amoxicillin degradation as a novel photocatalyst in aqueous solutions under visible light radiation. Various diagnostic methods were used to determine the morphology and functional structure of the photocatalyst, and the results confirmed its proper formation. Complete degradation of AMX was obtained at a pH of 5, catalyst dosage of 0.4 g/L, AMX concentration of 10 mg/L, and reaction time of 60 min. The efficiency of the degradation was diminished when anions were present in the reaction medium, and the order of their effect was SO42- < Cl- < NO3- < HCO3-. Biodegradability (BOD5/COD ratio) increased from 0.20 to 0.68 after 120 min of photocatalytic treatment, with a COD removal of 87.54% and a TOC removal of 74.88%. Through the experimental trapping of electrons, we found the production of reactive species, such as hydroxyl radical (•OH), superoxide (O2•-), and holes (h+), in the photocatalysis reactor and that •OH was the predominant species in AMX photodegradation. Comparative experiments emphasized that the oxidation process occurs with the adsorption of pollutants on the surface of the catalyst, and the photocatalyst has the potential to be activated by various light sources, including visible light, UV light, and sunlight, with an AMX decomposition above 88%. The synthesized particles can be recovered after five consecutive cycles with minimal reduction in the degradation rate (< 4%). γ-Fe2O3@SiO2@ZIF8-Ag can be considered a promising photocatalyst for use in AMX degradation due to its recyclability, easier activation by different light sources, and excellent mineralization.

Removal of Benzene and Toluene from Synthetic Wastewater by Adsorption onto Magnetic Zeolitic Imidazole Framework Nanocomposites.

Considering the risk associated with exposure to benzene and toluene in water resources, researchers have been motivated to conduct studies to remove them from aqueous solutions. Thus, by performing the present study, the potential of Fe3O4/zeolite imidazolate framework nanoparticles (Fe3O4@ZIF-8) was evaluated for the adsorption of benzene and toluene. Accordingly, the solution pH, Fe3O4@ZIF-8 dosage, mixing time, concentration of benzene and toluene, and temperature, were the parameters considered for conducting the batch experiments, for which their effect on adsorption efficiency was evaluated. Our conducted experiments introduced the neutral pH as the best pH range to obtain the maximum removal. Fitting the adsorption data into the various models revealed the aptness of the Langmuir isotherm equation in describing experimental information and highest adsorption capacity; for benzene it was 129.4, 134.2, 137.3, and 148.2 mg g-1, but for toluene it was 118.4, 125.2, 129.6, and 133.1 mg g-1, for temperature 20, 30, 40, and 50 °C, respectively. Using obtained optimal conditions, the adsorption efficiencies of benzene and toluene were obtained to be 98.4% and 93.1%, respectively. Kinetic studies showed acceptable coefficients for PSO kinetics and confirmed its suitability. Also, the recyclability results showed that for six consecutive periods of the adsorption-desorption process, the percentage of removal decreased by only 6% for benzene and toluene. Moreover, calculating thermodynamic parameter changes for benzene and toluene removal confirmed the favorability and spontaneity of the studied process and its endothermic nature. Considering the above findings, Fe3O4@ZIF-8 was found to be an operative adsorbent for removing pollutants.

Capability of copper-nickel ferrite nanoparticles loaded onto multi-walled carbon nanotubes to degrade acid blue 113 dye in the sonophotocatalytic treatment process.

In this study, copper-nickel ferrite (CuNiFe2O4) nanoparticles were successfully loaded onto multi-walled carbon nanotubes (MWCNTs) by using the coprecipitation method and used as new catalysts (MWCNT-CuNiFe2O4) in the sonophotocatalytic degradation process of the acid blue 113 (AB113) dye. The success of the MWCNT-CuNiFe2O4 synthesis and its properties were determined by analyzing it using field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). A high efficiency of dye removal (100%), total organic carbon (93%), and chemical oxygen demand (95%) were achieved with the following conditions: pH of dye solution = 5, MWCNT-CuNiFe2O4 dosage = 0.6 g/L, AB113 dye concentration = 50 mg/L, UV light intensity = 36 W, ultrasonic wave frequency = 35 kHz, and treatment time = 30 min. The kinetic results revealed that the efficiency of the sonophotocatalytic process using MWCNT-CuNiFe2O4 was higher than that of the sonolysis, photolysis, photocatalysis, and sonocatalysis processes. Scavenging studies demonstrated that the holes (h+) and hydroxyl radical (•OH) were the main reactive species for the AB113 dye degradation. The stability and recyclability of MWCNT-CuNiFe2O4 were confirmed with eight consecutive cycles for a maximum efficiency of more than 92%. The high rate of BOD5/COD indicated that the sonophotocatalytic process had the potential to degrade the dye into degradable compounds. The toxicity study with an Escherichia coli growth inhibition rate emphasized that MWCNT-CuNiFe2O4 in the sonophotocatalytic degradation process of the AB113 dye had a significant effect on reducing toxicity, when compared to processes of photolysis and photocatalysis. During the sonophotocatalytic process using MWCNT-CuNiFe2O4, the AB113 dye was mineralized into CO2, H2O, NH4+, NO3-, and SO42-. The results of the present study proved that the MWCNT-CuNiFe2O4-based sonophotocatalytic process was a promising dye degradation technology to protect the aquatic environment.

Adsorptive Removal of Azithromycin Antibiotic from Aqueous Solution by Azolla Filiculoides-Based Activated Porous Carbon.

Due to the shortage of freshwater availability, reclaimed water has become an important source of irrigation water. Nevertheless, emergent contaminants such as antibiotics in reclaimed water can cause potential health risks because antibiotics are nonbiodegradable. In this paper, we report the adsorptive removal of azithromycin (AZM) antibiotics using activated porous carbon prepared from Azolla filiculoides (AF) (AFAC). The influence of the adsorption process variables, such as temperature, pH, time, and adsorbent dosage, is investigated and described. The prepared AFAC is very effective in removing AZM with 87% and 98% removal after the treatment of 75 min, at 303 and 333 K, respectively. The Langmuir, Temkin, Freundlich, and Dubinin-Radushkevich isotherm models were used to analyze the adsorption results. The Freundlich isotherm was best to describe the adsorption isotherm. The adsorption process follows second-order pseudo kinetics. The adsorption was endothermic (ΔH°= 32.25 kJ/mol) and spontaneous (ΔS° = 0.128 kJ/mol·K). Increasing the temperature from 273 to 333 K makes the process more spontaneous (ΔG° = -2.38 and -8.72 KJ/mol). The lower mean square energy of 0.07 to 0.845 kJ/mol confirms the process' physical nature. The results indicate that AFAC can be a potential low-cost adsorbent of AZM from aqueous solutions.

Activated carbon derived from Azolla filiculoides fern: a high-adsorption-capacity adsorbent for residual ampicillin in pharmaceutical wastewater.

In this study, the effectiveness of activated carbon prepared from the Azolla filiculoides fern (ACAF) in order to remove ampicillin from aqueous solution was examined. The preparation of the ACAF was performed through chemical and physical activation processes with the presence of ZnCl2 and at a temperature of 450 °C. The ACAF yield was 44.7% of the fresh Azolla filiculoides. The results obtained from the characterization study indicate that the prepared ACAF has excellent surface and internal properties to be used as an adsorbent. The surface area, porosity, and pore volume were estimated to be 716.4 m2/g, 51.2%, and 0.621 cm3/g, respectively. The functional groups in ACAF that were responsible for the adsorption of ampicillin molecules were detected using FTIR analyses. The maximum efficiency (96.84%) and uptake (114.3 mg/g) of ACAF to remove ampicillin were achieved under the following conditions: ACAF dose = 0.8 g/L, pH = 7, concentration of ampicillin = 100 mg/L, contact time = 60 min, and temperature = 45 °C. It was found that the kinetic and isotherm data matched the pseudo-second-order and Langmuir models with high precision values, respectively. Considering the thermodynamics of the adsorption, the endothermic and spontaneous nature of the ampicillin adsorption onto ACAF was approved. The ampicillin adsorption capacity by ACAF was not significantly affected by the presence of different concentrations of NaNO3 competitor ion. The considerably higher adsorption capacity of the ACAF for ampicillin (114.3 mg/g) than other previously used adsorbents with excellent regeneration level (five cycles) depicts the superior performance of ACAF in the adsorption systems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13399-021-01962-4.

Photocatalytic degradation of amoxicillin from aqueous solutions by titanium dioxide nanoparticles loaded on graphene oxide.

The photocatalytic degradation of amoxicillin (AMX) by titanium dioxide nanoparticles loaded on graphene oxide (GO/TiO2) was evaluated under UV light. Experimental results showed that key parameters such as initial pH, GO/TiO2 dosage, UV intensity, and initial AMX concentration had a significant effect on AMX degradation. Compared to the photolysis and adsorption processes, the AMX degradation efficiency was obtained to be more than 99% at conditions including pH of 6, the GO/TiO2 dosage of 0.4 g/L, the AMX concentration of 50 mg/L, and the intensity of 36 W. Trapping tests showed that all three hydroxyl radical (OH•), superoxide radical (O2•-), and hole (h+) were produced in the photocatalytic process; however, h+ plays a major role in AMX degradation. Under UV irradiation, GO/TiO2 showed excellent stability and recyclability for 4 consecutive reaction cycles. The analysis of total organic carbon (TOC) suggested that AMX could be well degraded into CO2 and H2O. The formation of NH4+, NO3-, and SO42- as a result of AMX degradation confirmed the good mineralization of AMX in the GO/TiO2/UV process. The toxicity of the inlet and outlet samples of the process has been investigated by cultivation of Escherichia coli and Streptococcus faecalis, and the results showed that the condition is suitable for the growth of organisms. The photocatalytic degradation mechanism was proposed based on trapping and comparative tests. Based on the results, the GO/TiO2/UV process can be considered as a promising technique for AMX degradation due to photocatalyst stability, high mineralization efficiency, and effluent low toxicity.

Development of sonophotocatalytic process for degradation of acid orange 7 dye by using titanium dioxide nanoparticles/graphene oxide nanocomposite as a catalyst.

In the present study, the sonophotocatalytic degradation of acid orange 7 (AO7) dye was evaluated. The catalyst used was the titanium dioxide nanoparticles/graphene oxide (TiO2/GO) nanocomposite, which was synthesized using the Hummers and Hoffman's method and the liquid phase deposition method. TiO2/GO nanocomposite was characterized through the analyses of transmission electron microscopy (TEM), X-ray diffraction (XRD), Energy Dispersive X-ray (EDX) spectroscopy, Raman spectroscopy, and Fourier transform infrared (FTIR) spectroscopy. In addition, properties of the surface area and pore size were determined by N2 adsorption-desorption and the Barrett-Joyner-Halenda methods. After modification, the nanocomposite properties showed successful stabilization of TiO2 on the graphene substrate and reduction of the recombinant carrier loads. By utilizing the proposed treatment, complete degradation of AO7 could be achieved under optimal operating parameters (pH = 5, initial concentration of AO7 dye = 50 mg/L, TiO2/GO nanocomposite dose = 0.5 g/L, UV light intensity = 36 W, ultrasonic wave intensity = 35 kHz, and reaction time = 30 min). Scavenging experiments confirmed that OH and h+ radicals were the predominant species in the sonophotocatalytic degradation reactions of the AO7 dye. The stability study confirmed the excellent shelf life of the TiO2/GO nanocomposite, with only a slight reduction in the degradation efficiency of the AO7 dye (<8.27%) detected, after six consecutive cycles of the sonophotocatalytic process. Studies related to the degradability of the AO7 dye and the biodegradability of the effluent from the process showed that the applied sonophotocatalytic system was able to remove the TOC concentration by 83% after a reaction time of 30 min. Moreover, the increase in the BOD5/COD ratio was also a confirmation for the increase in biodegradability of the treated AO7 dye effluent. Finally, the toxicity test showed that the growth inhibition rate of Escherichia coli (E. coli), as a viability index, decreased to about 7.34% after a reaction time of 180 min. This result indicated the formation of compounds with low toxicity and molecular weight over the reaction time of the sonophotocatalytic process of AO7 dye.

Utilization of MWCNTs/Al2O3 as adsorbent for ciprofloxacin removal: equilibrium, kinetics and thermodynamic studies.

In the present study, the adsorption behavior of ciprofloxacin (CIP) from aqueous solution onto MWCNTs/Al2O3 was studied using batch experiments. Physical characterization of MWCNTs/Al2O3 was determined by SEM, XRD, and BET. The effective parameters investigated included: initial CIP concentration, contact time, MWCNTs/Al2O3 mass, and temperature. Based on experimental results and correlation coefficients, the rate of CIP adsorption followed the pseudo-second-model kinetics. Complete compatibility of the adsorption isotherm process was achieved with the Langmuir model, and the maximum adsorption capacity reached 41.73 mg/g under the optimized conditions (pH = 7, MWCNTs/Al2O3 dose = 1.2 g/L, contact time = 60 min, initial concentration = 10 mg/L, and temperature= 45 °C). The adsorption capacities based on the Langmuir model at different temperatures, 273, 288, 303, and 318 K, were equal to 72.18, 75.92, 79.65, and 83.47 mg/g, respectively. The determined parameters of the thermodynamic studies demonstrated the endothermic and spontaneous nature of the biosorption. The mean free energy was estimated from D-R isotherm model to be 0.316-0.707 KJ/mol, which clearly proved that the adsorption experiment followed a physical process. The data suggest that MWCNTs/Al2O3 could be used as a highly effective adsorbent material with a high capacity for the removal of antibiotics from water and wastewater.

Human health risk assessment of trace elements in drinking tap water in Zahedan city, Iran.

Daily intake of elements through the consumption of drinking water, due to its detrimental effects, is accounted for an important concern. Although the health risk assessment of heavy metals in different water sources has extensively carried out in various studies, the effect of age and the concentration of all trace elements in drinking tap water have neglected. Therefore, this study was conducted to evaluate the concentrations of heavy metals, e.g., As, Cd, Cr, Ni, Pb, B, Al, Hg, Mn, Zn, Cu, Fe, Se and Ba in the drinking tap water of Zahedan city and to estimate their non-carcinogenic and carcinogenic effects. Moreover, this is the first research in Iran that has also been dedicated to complete investigation on daily intakes of trace elements in tap water. A total of 155 samples of drinking water were randomly taken from the tap water and were analyzed using ICP-OES device. The estimation of the carcinogenic and non-carcinogenic risks of analyzed elements was carried out based on the guidelines of the U.S EPA. The hazard index (HI) values for children and adult age groups were 9.84E-01 and 4.22E-01, respectively. The cumulative Excess Lifetime Cancer Risk (ELCR) for carcinogenic trace elements was in range of tolerable carcinogenic risk 10-6 to10-4 and for all carcinogenic elements were in the order of Pb > Cd > Cr. It also detected that the total carcinogenic risks of the Cd, As and Cr in water samples through the ingestion route are at the levels of "low risk" and "low-medium risk".

An overview report on the application of heteropoly acids on supporting materials in the photocatalytic degradation of organic pollutants from aqueous solutions.

Organic pollutants contaminate water resources and the environment when discharged into water streams. Also, the presence of these materials in incompletely treated or untreated wastewater leads to serious environmental hazards. The hydroxyl radicals and holes are regarded as the most oxidant species in the degradation of organic pollutants using the studied composites. The results of this review show that heteropoly acids on supporting materials could be considered as appropriate photocatalysts in the removal of organic pollutant from aqueous solutions.

Probabilistic risk assessment of exposure to fluoride in most consumed brands of tea in the Middle East.

The aim of this study was to evaluate the fluoride concentration in seven most consumed brands of tea in the Middle East which was imported to Iran through Zabol County. In the present study, the health risk of exposure to fluoride was estimated using a probabilistic approach. Monte Carlo simulation and sensitivity analysis were applied to quantify uncertainties in risk estimation. The highest mean and 95th percentile of chronic daily intake (CDI) was observed for children group. Iranian tea and Kenya tea had maximum CDI and target hazard quotient (THQ) values among studied brands of tea which followed by Green tea, Taksetare tea, Ceylan tea, Red tea, and White tea. These result indicated that there were significant risks of exposure to fluoride in most of studied brands of tea for children (THQ>1). Sensitivity analysis showed that fluoride concentration and daily intake were the most influential variables in three exposed populations. In conclusion, the fluoride concentration in some studied brands of tea is high and it put children at risk risks of exposure to fluoride.

Relationship between musculoskeletal disorders and anthropometric indices among bus drivers in Zahedan city.

INTRODUCTION: Most work-related musculoskeletal disorders (MSDs) are associated with improper postures and poorly designed workstations. This study is an attempt to examine the prevalence and severity of MSDs as well as anthropometric dimensions among city bus drivers. METHODOLOGY: This cross-sectional study was carried out on 60 male bus drivers. A body discomfort chart was used to evaluate MSDs. Spearman correlation was employed to examine the relationship between body size and the severity of discomfort. RESULTS: Data analysis showed that discomfort reported in the lower back (33.3%), upper back (18.3%) and knee (15%) was severe and there was a direct and significant correlation between the body mass index and the severity of discomfort in the shoulder, arm and hip (p < 0.05). However, the results showed that eye sitting height and sitting height had significant inverse relationships with discomfort in the ankle and elbow (p < 0.05). CONCLUSION: The results of the study can be used to address ergonomic risk factors and reduce their associated disorders. The findings of the study can be used in training programs to educate drivers how to decrease the risk associated with work-related MSDs by adopting appropriate behavior strategies.

Removing 2,4-dichlorophenol from aqueous environments by heterogeneous catalytic ozonation using synthesized MgO nanoparticles.

2,4-Dichlorophenol (2,4-DCP) is one of the seriously toxic chlorophenol compounds found in agricultural environments, in water disinfected by chlorine, and in outgoing effluents from the pulp and paper industries and paper manufacturing factories. This research studied the feasibility of using MgO nanoparticles (MgO-NPs) as a catalyst in the ozonation process for removing 2,4-DCP from aqueous environments under laboratory conditions. This study was conducted using a laboratory-scale semi-continuous reactor. It studied the effects of critical variables such as solution pH, ozonation time, dose of MgO-NPs and initial 2,4-DCP concentration. A statistical model of response surface model (RSM) was designed and utilized to obtain the optimum experimental conditions. Analysis of the data showed that initial concentration of 2,4-DCP and dose of MgO-NPs had the maximum effect on the response variable (percentage degradation of 2,4-DCP). Moreover, based on analysis of variance on the model, the optimum removal conditions were reaction time of 50 min, pH > 7, initial 2,4-DCP concentration of less than 50 mg/L, and an MgO-NPs dose of 0.3 mg/L. Under these optimum conditions, a removal efficiency of 99.99% was achieved. In addition, results indicated that catalytic ozonation in the presence of MgO-NPs was very efficient at removing 2,4-DCP from aqueous environments.

Studies on the adsorption of amoxicillin on multi-wall carbon nanotubes.

This study examined the feasibility of removing amoxicillin (AMO) from aqueous solutions using multi-wall carbon nanotubes. The equilibrium adsorption data were analyzed using four widely applied isotherms: Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich. The results showed that the Langmuir isotherm model fits well the obtained experimental data. The adsorption process followed the pseudo-second-order model. The activation energy was found to be 19 kJ/mol. The Standard free energy changes, ΔG0, values were negative; the standard enthalpy change (ΔH0), and standard entropy change (ΔS0) values of the process were 4 kJ/mol and 36 J/mol.K. Results suggested that the AMO adsorption on carbon nanotubes was a spontaneous process.

Investigation of Parasitic Contaminations of Vegetables Sold in Markets in the City of Tabriz in 2014.

Parasitic diseases are among the most common problems in developing countries. Various parasitic forms such as cysts, larvae and eggs of the parasite are transmitted orally through the consumption of vegetables. So, the aim of this study was to evaluate parasitic contamination of fresh vegetables consumed in the city of Tabriz. This cross-sectional study was conducted for 3 months in 2014 in Tabriz. In this study, 1620 samples from 10 kinds of vegetables (leeks, basil, mint, chives, radishes, parsley, lettuce, watercress, tarragon and coriander) were collected from 54 vegetable shops. After the washing process, centrifugation, sediment preparation and staining, each sample was examined for parasitic contamination. The parasitic infection was observed in 316 (19.5%) which 141 samples (8.7%) was related to metazoan and 175 samples (10.8%) was related to protozoan. the highest contamination was observed in leeks and the lowest in radish. Most parasitic contaminations were related to Ascaris eggs and E. coli cyst and the lowest parasitic contaminations were related to Heterophyes eggs. It can be concluded that vegetables sold in Tabriz are potential sources of human contamination with parasites. It is suggested that the use of fertilizers of human source in agriculture should be avoided.

Prevalence of Intestinal Parasitic Infection among Food Handlers in Northwest Iran.

Parasitic diseases are among the most important infectious diseases and pose health problems in many countries, most especially in developing countries. Workers at food centers could transmit parasitic infections in the absence of sanitation. This is a descriptive study conducted to determine the prevalence of intestinal parasitic infections in food clerks in the city of Tabriz in 2014. Data was recorded in the offices of the health center for all food handlers who were referred to the laboratory for demographic and stool tests to receive the health card. Parasitic infection was observed in 172 cases (3.73%) of 4612 samples. A total of 156 positive samples (90.69%) were related to protozoa and 16 (9.3%) were related to helminthes. Most of the parasitic infections were related to Giardia and Entamoeba coli and the lowest infection was related to H. nana. Also, there was a significant relationship between level of education and parasitic infection rate (P = 0.0044). But there was no significant difference between the type of infection and amount of intestinal parasites. The results show that the prevalence of intestinal parasites, especially pathogenic protozoa, is common in some food handlers. Therefore, more sanitary controls are required and increasing of education will play a crucial role in improving the health of these people.

Phytodegradation potential of bisphenolA from aqueous solution by Azolla Filiculoides.

Many organic hazardous pollutants such as bisphenolA (BPA) which are toxic and not easily biodegradable can concerns for environmental pollution worldwide. The objective of this study was to examine whether Azolla Filiculoides is able to remove BPA from aqueous solutions. In this study, the Azolla with different biomass (0.3, 0.6, 0.9, 1.2 g) has been cultured in solution that was contained 5, 10, 25 and 50 ppm BPA. Samples were collected every 2 days from all of containers. The analytical determination of BPA was performed by using of DR4000 uv-visible at λmax = 276 nm. The results indicated that Azolla has high ability to remove BPA from aqueous solutions. The BPA removal was 60-90%. The removal efficiency is increasing with decreasing of BPA concentration and increasing of biomass amount and vice versa. The removal efficiency was more than 90% when BPA concentration was 5 ppm and amount of biomass was 0.9gr. It is concluded that Azolla able remove BPA by Phytodegradation from the aqueous solutions. Since conventional methods of BPA removal need to high cost and energy, phytoremediation by Azolla as a natural treatment system can decrease those issues and it can be a useful and beneficial method to removal of BPA.