18 research outputs found

    PRECONCENTRATION OF CADMIUM USING AMBERLITE XAD-4 PRIOR TO ATOMIC ABSORPTION SPECTROMETERY

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    Cadmium is an important environmental constituent widely used in industrial processes for production of synthetic materials and therefore can be released in the environment causing public exposure especially around the industrial residence area. For evaluation of human exposure to trace toxic metal of Cd (II), environmental and biological monitoring are essential processes, in which, preparation of such samples is one of the most time-consuming and error-prone aspects prior to analysis. The use of solid-phase extraction (SPE) has grown and is a fertile technique of sample preparation as it provides better results than those produced by liquid-liquid extraction (LLE). To evaluate factors influencing quantitative analysis scheme of cadmium in water samples, solid phase extraction using mini columns filled with XAD-4 resin was optimized with regard to sample pH, ligand concentration, loading flow rate, elution solvent, sample volume (up to 500 ml), elution volume, amount of resins, and sample matrix interferences. Cadmium was retained on solid sorbent and eluted followed by simple determination of analytes by using flame atomic absorption spectrometery. Obtained recoveries of the metal ion were more than 92%. The amount of the analyte detected after simultaneous preconcentration was basically in agreement with the added amounts. The optimized procedure was also validated with three different pools of spiked urine samples and showed a good reproducibility over six consecutive days as well as six within-day experiments. The developed method promised to be applicable for evaluation of other metal ions present in different environmental and occupational samples as suitable results were obtained for relative standard deviation (less than 10%); therefore, it is concluded that, this optimized method can be considered to be successful in simplifying sample preparation for trace residue analysis of Cd in different matrices for evaluation of occupational and environmental exposures

    Evaluation of Nuisance Dust Health Effects on the Workers in a Tile Industry

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    Background and objectivesAir pollution in the occupational fields and its economical effects on the health care system is studied from different viewpoints such as products quality, equipment damage, environment preservation, and air pollution control. Nowadays, a lot of attention has been turned toward health effects of air pollution. The objective of this study is detection of the total dust concentration and assessment of the health effect of nuisance dust among workers in a tile production factory.MethodsIn this study airborne dust concentration was measured and evaluated by using NIOSH 0500 method. In order to determine the health effects, a standard questionnaire was used. All of personnel of workshop 1 (n=50) and workshop 2 (n=50) were assigned to the case group and one hundreds of factory employees were assigned to the control group. Results analyzed using Z test.ResultsAccording to the obtained results, concentration of dust in workshop 1 corridor was higher than that of workshop 2 corridor (59.262 mg/m3 and 32.158 mg/m3 respectively). Also, these results showed that there are significant differences between two groups in incidence of symptoms such as dry cough, eye irritation, skin redness, shortness of breath, blurred vision, skin irritation, hoarseness of voice, dry mouth and throat, throat itching and skin itching (P<0.05). However, there were not significant differences in incidence of headache, chest pain, epiphora of eyes, mucus cough, sinus problems and chest wheezing between two groups.ConclusionOn the basis of these results it was revealed that nuisance dust can affect human health and performance. This in turn can increase the medical service load and costs. As a result of inadequate control systems established in the industries, lack of information and appropriate training, and lack of personal protective equipment all across the industries, we suggest a more comprehensive research project to evaluate the effects of industrial air pollution on the workers in order to improve quality of their lives and work.Keywords: Air Pollution; Dust; Nuisance; Health Effects; Tile Industr

    Molecularly Imprinted Solid Phase Extraction For Trace Analysis Of Diazinon In Drinking Water

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    Amongst organophosphate pesticides, the one most widely used and common environmental contaminant is diazinon; thus methods for its trace analysis in environmental samples must be developed. Use of diazinon imprinted polymers such as sorbents in solid phase extraction, is a prominent and novel application area of molecular imprinted polymers. For diazinon extraction, high performance liquid chromatography analysis was demonstrated in this study. During optimization of the molecular imprinted solid phase extraction procedure for efficient solid phase extraction of diazinon, Plackett-Burman design was conducted. Eight experimental factors with critical influence on molecular imprinted solid phase extraction performance were selected, and 12 different experimental runs based on Plackett-Burman design were carried out. The applicability of diazinon imprinted polymers as the sorbent in solid phase extraction, presented obtained good recoveries of diazinon from LC-grade water. An increase in pH caused an increase in the recovery on molecular imprinted solid phase extraction. From these results, the optimal molecular imprinted solid phase extraction procedure was as follows: solid phase extraction packing with 100 mg diazinon imprinted polymers; conditioning with 5 mL of methanol and 6 mL of LC-grade water; sample loading containing diazinon (pH=10); washing with 1 mL of LC-grade water, 1 mL LC- grade water containing 30% acetonitrile and 0.5 mL of acetonitrile, respectively; eluting with 1 mL of methanol containing 2% acetic acid. The percentage recoveries obtained by the optimized molecular imprinted solid phase extraction were more than 90% with drinking water spiked at different trace levels of diazinon. Generally speaking, the molecular imprinted solid phase extraction procedure and subsequent high performance liquid chromatography analysis can be a relatively fast and proper approach for qualitative and quantitative analysis of diazinon in drinking water

    Optimization of Solid Phase Micro-Extraction (SPME) for Monitoring Occupational Exposure to Ethyl Benzene

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    AbstractBackground and Objectives: Analytical methods for volatile organic compounds (VOCs) in different samples need extraction of compounds, by applying hazardous solvents. Solid phase micro-extraction (SPME) is a solvent-free equilibrium extraction method, in which proper calibration can allow quantitative determinations of VOCs at a very good sensitivity without the use of any organic solvent. VOCs are generally present in urine only at trace levels, therefore, a sensitive procedure is needed for their trace determinations. Throughout this study, headspace solid phase micro-extraction (HS-SPME) was followed by GC-FID for ethyl benzene in spiked urine was optimized.Methods: In this study, the parameters influencing SPME and gas chromatography of ethyl benzene, including extraction time, temperature, desorption temperature, desorption time, salt addition, sample pH, sample volume and sample agitation were investigated. Results: Extraction procedure was performed at 30°C for 6 min, using 0.2 gml-1 of NaCl in the sample solution. The sample volume and sample pH were optimized at 5 ml and 7 (neutral pH), respectively. Desorption of the ethyl benzene was carried out for 60 sec. at 250°C. The method was also validated with three different spiked urine samples and illustrated an appropriate reproducibility over six consecutive days as well as six within-day experiments. During this investigation, parameters of accuracy, linearity, and detection limits of the procedure were also evaluated.Conclusion: The developed method of HS- SPME-GC-FID proved to be a simple, convenient, and practical procedure, and was successfully used for measuring of ethyl benzene in spiked urine

    Evaluating Poly-Aromatic Hydrocarbons in respiratory zone of the asphalt workers in Tehran city

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    Introduction: PAHs are organic compounds with benzenic rings that releas from hot asphalt as incomplete combusting. These compounds are one of the major concern in scientific societies, workplace and environment due to their stability, bioaccumulation, carcinogenic and mutagenic effects. Since asphalt workers are exposed to PAHs frequently in their job, in this study it was attempted to evaluate respiratory exposure of asphalt workers to PAHs in their breathing zone. .Material and Method: In this study air samples of the asphalt workers were collected in accordance with the NIOSH 5506 method using PTFE filter and XAD-2 adsorbent. The ultrasonic bath and acetonithrile are used in order to extract the analytes from the filter and adsorbent. Also, the samples were analyzed by HPLC-UV. .Result: In all samples, Finisher assistance and oilman with 1754.48 ng/m3 , 24.65 ng/m3 had maximum and minimum exposed to ∑PAH, respectively. Among the PAHs compounds, which asphalt workers exposed to, Naphtalene had the highest concentration. Among different asphalt workers tasks, screedman expoused to PAHs, had a significant difference. . Conclusion: Evaluation of Polycyclic aromatic hydrocarbons concentrations in the breathing zone of asphalt workers indicated that exposure to these compounds were below the occupational exposure limits recommended by NIOSH, OSAH, ACGIH and Iranian OEL. Due to the highly carcinogenic potential of some of these compounds and absence of occupational exposure limits for these compounds, likes Chrysene and Benzo (a) Anthracene, it is strictly recommended to employ engineering controls and using suitable PPEs. This study also indicated that the exposure to PAHs in the most asphalt workers tasks had significant differences, and it can be due to proximity of the workers to the source of hot asphalt and also exposure to the exhaust gases that releasesd from the construction machinery

    SOLID PHASE MICROEXTRACTION FOR TRACE ANALYSIS OF URINARY BENZENE IN ENVIRONMENTAL MONITORING

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    Conventional analytical method for organic pollutants in water requires extraction of the pollutants, using hazardous solvent. Solid phase microextraction is a solvent free equilibrium extraction method, in which, proper calibration can allow quantitative determinations of organic pollutants at a very good sensitivity without the use of any organic solvent. Because individual volatile organic carbons are generally exposed environmentally and present in urine only at trace levels, a sensitive and accurate determination technique is essential. So, this study describes the optimization of headspace solid phase microextraction (HS-SPME) followed by GC-FID for benzene in spiked urine. Through this investigations, the parameters affecting the extraction and gas chromatographic determination of analytes, including extraction time, temperature, desorption temperature, desorption time, salt addition, sample pH, sample volume and sample agitation were studied. An optimized headspace extraction was carried out at 30°C for 6 min in the presence of 0.2 g/mL of NaCl in the sample solution. Desorption of the analytes was carried out for 60 sec. at 250°C. The optimized procedure was also validated with three different pools of spiked urine samples and showed a good reproducibility over six consecutive days as well as six within-day experiments. The accuracy, linearity, detection limits were also determined. The headspace solid phase microextraction, GC-FID technique provides a relatively simple, convenient, practical procedure, which was here successfully applied to determine benzene in spiked urine

    Chlorpyrifos remediation in agriculture runoff with homogeneous solar photo-Fenton reaction at near neutral pH: Phytotoxicity assessment

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    This study represents the first application of Fe-citrate-based photo-Fenton chemistry for the degradation of chlorpyrifos (CPF) spiked into agricultural runoff, and its phytotoxicity assessment. The effects of the initial CPF concentration, time and ratio of Fe-citrate/H2O2 on CPF removal during the photo-Fenton reaction were investigated and modeled with analysis of variance using R software by the response-surface methodology package. According to the stationary point in original units, the optimal condition for 70.00 CPF removal was as follows: CPF = 2.5 mg L-1 (0.0), time = 48.0 min (0.585) and Fe-citrate/H2O2 = 0.075 (0.539). Beside running the system at near-neutral pH, another strength of this study is related to the treatment of agricultural runoff contaminated with CPF with a raceway pond reactor, which has the advantages of simplicity of the facilities and procedures, as well as the possibility of using sunlight more efficiently in the field of applications. Finally, untreated and treated agriculture runoffs were used as irrigation to determine their phytotoxic effects on seed germination of cress (Lepidium sativum). Solar photo-Fenton treatment greatly reduced phytotoxicity of agriculture runoff and showed the highest germination percentage (70) compared to both raw agricultural runoff (60) and untreated CPF-spiked runoff (35). © IWA Publishing 2021 Water Science & Technolog

    Molecular Imprinted Solid Phase Extraction For Determination Of Atrazine In Environmental Samples

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    Solid phase extraction is one of the major applications of molecularly imprinted polymers fields for clean-up of environmental and biological samples namely molecularly imprinted solid-phase extraction. In this study, solid phase extraction using the imprinted polymer has been optimized with the experimental design approach for a triazine herbicide, named atrazine with regard to the critical factors which influence the molecular imprinted solid phase extraction efficiency such as sample pH, concentration, flow-rate, volume, elution solvent, washing solvent and sorbent mass. Optimization methods that involve changing one factor at a time can be laborious. A novel approach for the optimization of imprinted solid-phase extraction using chemometrics is described. The factors were evaluated statistically and also validated with spiked water samples and showed a good reproducibility over six consecutive days as well as six within-day experiments. Also, in order to the evaluate efficiency of the optimized molecularly imprinted solid-phase extraction protocols, enrichment capacity, reusability and cross-reactivity of cartridges have been also evaluated. Finally, selective molecularly imprinted solid-phase extraction of atrazine was successfully demonstrated with a recovery above 90% for spiked drinking water samples. It was concluded that the chemometrics is frequently employed for analytical method optimization and based on the obtained results, it is believed that the central composite design could prove beneficial for aiding the molecularly imprinted polymer and molecularly imprinted solid-phase extraction development
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