Natural radioactivity levels and radiation hazard indices in granite from Aswan to Wadi El-Allaqi southeastern desert, Egypt

Studies on radiation level and radionuclide distribution in granite from Aswan to Wadi El-Allaqi area that is located in southeastern desert of Egypt were undertaken. The samples collected from five locations: Gabal El Mesala, Umm Hibal, Abu Herigle, Abu Marw and Deneibit El Quleib. The purpose of this study is to provide a baseline map of radioactivity background levels in the investigated area environment, and this study will be used as reference information to assess any changes in the radioactive background level due to geological processes. The highest average values of 226Ra and 232Th concentrations (24.00 and 31.28 Bq kg(-1), respectively) were observed at Abu Herigle region, whereas the highest average value of 40K concentration, 589.95 Bq kg(-1), was detected in Umm Hibal. The absorbed dose rate in air was found to be in the range between 5.40 and 45.11 nGy h(-1), and radium equivalent activity concentration was found in the range between 29.57 and 71.85 Bq kg(-1). Also the representative external hazard index values for the corresponding samples were also estimated and given.     

Natural radionuclides and dose estimation in natural water resources from Elba protective area, Egypt

The concentrations of the natural radionuclides (226)Ra, (232)Th and (40)K in 15 different water samples from Elba protective area, south-eastern desert of Egypt, have been determined using NaI(Tl) detector. Gamma ray spectrometric analysis was performed and the concentrations obtained for each of the radionuclides expressed in Bq l(-1) ranging from 1.6 to 11.1 for (226)Ra, 0.21 to 0.97 for (232)Th and 9.1 to 23 for (40)K. A reasonable correlation was found between (226)Ra, (232)Th concentrations and pH, although no general trend was observed with conductivity and total dissolved solids. The mean effective doses of 0.56 mSv y(-1) for (226)Ra, 0.065 mSv y(-1) for (232)Th and 0.04 mSv y(-1) for (40)K were estimated for the ingestion of these waters by adults.     

Assessment of natural radioactivity concentrations and gamma dose rate levels in Kayseri, Turkey

This study assesses the level of background radiation for Kayseri province of Turkey. Natural radionuclide activity concentrations in soil samples were determined using high-resolution gamma spectroscopy. Outdoor gamma dose measurements in air at 1 m above ground level were determined using a portable gamma scintillation detector. The obtained results of uranium and thorium series as well as potassium ((40)K) are discussed. The present data were compared with the data obtained from different areas in Turkey. From the measured gamma-ray spectra, the average activity concentrations were determined for (238)U (range from 3.91 to 794.25 Bq kg(-1)), (232)Th (range from 0.68 to 245.55 Bq kg(-1)) and (40)K (range from 23.68 to 2718.71 Bq kg(-1)). The average activity concentrations of (238)U, (232)Th and (40)K were found to be 35.51, 37.27 and 429.66 Bq kg(-1), respectively, and 11.53 Bq kg(-1) for the fission product (137)Cs. The highest values of (238)U, (232)Th and (40)K concentrations (794.25 Bq kg(-1), 245.55 Bq kg(-1), 2718.71 Bq kg(-1), respectively) were observed in abnormal samples at Hayriye village. The average outdoor gamma dose rate in air at 1 m above the ground was determined as 114.43 nGy h(-1). Using the data obtained in this study, the average annual effective dose for a person living in Kayseri was found to be about 140.34 μSv.     

A comprehensive study of natural gamma radioactivity levels and associated dose rates from surface soils in cyprus

A survey was carried out to determine activity concentration levels and associated dose rates from the naturally occurring radionuclides 232Th, 238U and 40K, in the various geological formations of Cyprus, by means of high-resolution gamma ray spectrometry. A total of 115 representative soil samples were collected from all over the bedrock surface of the island, based on the different lithological units of the study area, sieved through a fine mesh, sealed in 1000 ml plastic Marinelli beakers and measured in the laboratory with respect to gamma radioactivity for a counting time of 18-h each. From the measured spectra, activity concentrations were determined for 232Th (range from 1.0 x 10(-2) to 39.8 Bq kg(-1)), 238U (from 1.0 x 10(-2) to 39.3 Bq kg(-1)) and (40)K (from 4.0 x 10(-2) to 565.8 Bq kg(-1)). Gamma absorbed dose rates in air outdoors were calculated to be in the range from 1.1 x 10(-2) to 51.3 nGy h(-1), depending on the geological features, with an overall mean value of 8.7 nGy h(-1) and a standard deviation of 8.4 nGy h(-1). This value is by a factor of about seven below the corresponding population-weighted world-averaged value of 60 nGy h(-1) and one of the lowest that has been reported from similar investigations worldwide. Assuming a 20% occupancy factor, the corresponding effective dose rates outdoors equivalent to the population were calculated to be between 1.3 x 10(-2) and 62.9 microSv y(-1), with an arithmetic mean value of 10.7 microSv y(-1) and a standard deviation of 10.3 microSv y(-1).     

Analysis of sulfonated naphthalene-formaldehyde condensates by ion-pair chromatography and their quantitative determination from aqueous environmental samples

An ion-pair solid-phase extraction (IPE), ion-pair chromatography (IPC) procedure with fluorescence detection for the quantitative analysis of sulfonated naphthalene-formaldehyde condensates (SNFC) was developed, which provides full resolution of SNFC up to a degree of condensation n = 5 and partial resolution up to n = 15. Liquid chromatography-electrospray ionization-mass spectrometry confirmed that SNFC elute in the order of condensation. Response factors in fluorescence detection proved to be mass-constant, thereby allowing us to determine total SNFC amounts. With this IPC method, the weight- and the number-average molecular weights of these high-volume production chemicals (kiloton per annum), used as synthetic tanning agents, concrete plasticizers, and dispersants, can be determined. Recoveries in IPE range from 73 to 85% in river Rhine water and from 79 to 93% in tap water for n = 2 to n = 7 with limits of detection of 3-8 ng/L for individual homologues from 500 mL of water. The IPE-IPC procedure was applied to samples of secondary industrial effluents, river Rhine water, a river bank filtrate, and a groundwater sample. SNFC up to n = 6 were detected in the treated effluents. Total concentrations ranged from 208 micrograms/L in a secondary treated SNFC production effluent to < 1.4 micrograms/L in groundwater. These first analyses suggest a widespread occurrence of the lower oligomers of SNFC in the aquatic environment.     

Specific activity and hazards of Archeozoic-Cambrian rock samples collected from the Weibei area of Shaanxi, China

The present work deals with the radioactivity of the Archeozoic-Cambrian rocks of the Weibei area, Shaanxi, China. A total of 45 rock samples of Archeozoic-Cambrian strata were investigated. The radionuclides of the samples, in Bq kg(-1), have been measured using Na(I)Tl gamma-ray spectrometer. The concentration of 226Ra, 232Th and 40K in the Archeozoic-Cambrian rock samples range from 12.3 to 55.4, from 2.4 to 98.7 and from 58.6 to 1613.3 Bq kg(-1), respectively. The measured activity concentrations for these radionuclides were compared with the typical world average values. To assess the radiological hazard of the natural radioactivity in the samples, the radium equivalent activity, the external hazard index, internal hazard index and the annual gonadal dose equivalent associated with the radionuclides were calculated and compared with the international recommended values.     

Potentiometric polymeric membrane electrodes for measurement of environmental samples at trace levels: new requirements for selectivities and measuring protocols, and comparison with ICPMS

It is here established that potentiometric polymeric membrane electrodes based on electrically neutral ionophores are useful analytical tools for heavy metal ion determinations in drinking water at nanomolar total concentrations. This means that they can compete with the most sophisticated techniques of instrumental analysis. With optimized ion-selective membranes based on the lead-selective ionophore 4-tert-butylcalix[4]arenetetrakis(thioacetic acid dimethylamide) as model example, a number of native and spiked drinking water samples are potentiometrically assessed for lead, and the results compared with ICPMS measurements. The goal of this work is to demonstrate that detection limits in real world samples are routinely achieved that are, with 1.5 ppb, at least 10-fold lower than the lead action limit imposed by the U.S. Environmental Protection Agency (15 ppb). In contrast to earlier reports, different conditioning and measuring protocols are followed, and membranes and inner filling solution of optimized composition are used. The sensors are shown to be useful for the speciation analysis of lead in water as well. Typical water samples are acidified to pH 4 to assess total lead rather than free, uncomplexed lead. For lead concentrations above 2 ppb, the values compare very well with ICPMS. Main interferences are found to be H+ and Cu2+, although Cu2+ only shows significant interference at levels around or above its own action limit (1.3 ppm), in which case the water sample would anyway show quality problems. An explicit, simplified flux model targeted to the practical use of these sensors explains the extent of expected interference. Sensors are shown to require a higher selectivity than predicted by models not considering ion fluxes, since in dilute samples, the counterdiffusion flux of lead from the membrane into the sample becomes potential determining. The model and experiments shown here are a foundation for future trace level applications of potentiometric polymeric membrane electrodes.     

Pressurized hot water extraction with on-line fluorescence monitoring: a comparison of the static,dynamic, and static-dynamic modes for the removal of polycyclic aromatic hydrocarbons from environmental solid samples

A comparison of the feasibility of the three operational modes of pressurized hot solvent extraction (PHSE) (namely, static, where a fixed extractant volume is used; dynamic, where the extractant continually flows through the sample; and static-dynamic mode, which consists of a combination of the two previous modes) for the extraction of polycyclic aromatic hydrocarbons (PAHs) from environmental solid samples (such as soil, sediment, trout, and sardine) has been performed. In all cases, a sodium dodecyl sulfate (SDS) aqueous solution was used as leaching agent. The use of a flow injection manifold between the extractor and a molecular fluorescence detector allowed real-time on-line fluorescence monitoring of the PAHs extracted from the samples, thus working as a screening system and providing qualitative and semiquantitative information on the target analytes extracted from both natural and spiked samples. The on-line monitoring option allowed the extraction kinetics to be monitored and the end of the leaching step to be determined independently of the sample matrix, thereby reducing extraction times. Efficiencies close to 100% have been provided by the three modes, which differ in the extraction time required for total removal of the target compounds. The time needed for the dynamic mode was shorter than that for the static mode. However, the establishment of a static extraction step prior to dynamic extraction was the key to shorten the time required for complete extraction. The method has been applied to a certified reference material (CRM 524, BCR, industrial soil/organics) for quality assurance/validation.     

Solid phase extraction of trace amounts of Ag, Cd, Cu, and Zn in environmental samples using magnetic nanoparticles coated by 3-(trimethoxysilyl)-1-propantiol and modified with 2-amino-5-mercapto-1,3,4-thiadiazole and their determination by ICP-OES

A fast, sensitive, and simple method using magnetic nanoparticles (MNPs) coated by 3-(trimethoxysilyl)-1-propantiol and modified with 2-amino-5-mercapto-1,3,4-thiadiazole, as an adsorbent has been successfully developed for extraction, preconcentration, and determination of trace amounts of Ag, Cd, Cu, and Zn from environmental samples. The prepared nanoparticles were characterized by Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). These magnetic nanoparticles can be easily dispersed in aqueous samples and retrieved by the application of external magnetic field via a piece of permanent magnet. The main factors affecting the extraction efficiency such as pH value, sample volume, eluent concentration and volume, ultrasonication time, and coexisting ions have been investigated and established. Under the optimal conditions, high concentration factors (194, 190, 170, and 182) were achieved for Ag, Cd, Cu, and Zn with relative standard deviations of 5.31%, 4.03%, 3.62%, and 4.20%, respectively. The limits of detection for Ag, Cd, Cu, and Zn were as low as 0.12, 0.12, 0.13 and 0.11 ng mL(-1). The prepared sorbent was applied for preconcentration of trace amounts of Ag, Cd, Cu, and Zn in the various water samples with satisfactory results.     

Soil contaminated with PAHs and nitro-PAHs: contamination levels in an urban area of Catania (Sicily,southern Italy) and experimental results from simulated decontamination treatment

This study is aimed at investigating the levels of polyaromatic hydrocarbons and nitro-polyaromatic hydrocarbons in polluted urban soils and the potential application of microwave heating as decontamination treatment. The soil samples were collected from an area of 0.05 km² of Catania (Sicily, southern Italy) rural site. HPLC in fluorescence and electrochemical–fluorescence detection mode were used for selective separation, identification and quantification of pollutants in soil samples. A bench-scale microwave treatment was performed irradiating a contaminated soil using different operating powers for removing both kinds of contaminants. Results reveal that soil pollutant concentrations were sometimes higher than those found in other locations. Polyaromatic and nitro-polyaromatic hydrocarbon levels observed suggest a strong contribution from incomplete combustion of gasoline or other fuels also due to the vicinity to the airport. Many polyaromatic hydrocarbon derivatives are more carcinogenic than the initial contaminant form and may have toxicological significance, even if present at much lower concentrations than their parent compounds. Thus, the environmental levels of these pollutants need to be monitored and removed. Contaminant removals from simulated microwave remediation show that the treatment is effective. Results also showed that contaminant features, especially polarity, significantly influence the dielectric properties of the soil and thus the final temperature reachable during the heating processes and the contaminant removals.