FIRST STEP TOWARDS THE GEOGRAPHICAL DISTRIBUTION OF INDOOR RADON IN DWELLINGS IN ALBANIA.

The realisation of the geographical distribution of the indoor radon concentrations in dwellings represents a valuable tool necessary for assessing the public exposure. In this work are reported the results of the indoor radon obtained in the first stage of the survey involving 247 measurements. From the preliminary information on ∼10 % of the territory, covering the biggest cities in Albania results on indoor radon concentrations ranging from 14 to 1238 Bq m-3 with an arithmetic mean of 120±67 Bq m-3 The population-weighted average indoor radon concentration was calculated to be 101 Bq m-3 The adopted survey strategy highlighted the necessity for the future stages to spread the measurements in order to cover the entire territory of Albania, instead of remaining focused only on the demographic criteria.

A century of oil and gas exploration in Albania: assessment of Naturally Occurring Radioactive Materials (NORMs).

The Naturally Occurring Radioactive Materials (NORMs) that are potentially generated from oil and gas extractions in Albania have been disposed of without regulations for many decades, and therefore, an extensive survey in one of the most productive regions (Vlora-Elbasan) was performed. A total of 52 gamma ray spectrometry measurements of soil, oil-sand, sludge, produced water and crude oil samples were performed. We discovered that relatively low activity concentrations of (226)Ra, (228)Ra, (228)Th and (40)K, with concentrations of 23±2Bq/kg, 23±2Bq/kg, 24±3Bq/kg and 549±12Bq/kg, respectively, came from the oil-sands produced by the hydrocarbon extraction of the molasses formations. The mineralogical characterizations and the (228)Ra/(40)K and (226)Ra/(40)K ratios of these Neogene deposits confirmed the predictions of the geological and geodynamic models of a dismantling of the Mesozoic source rocks. The average activity concentrations (±standard deviations) of the radium isotopes ((226)Ra and (228)Ra) and of the (228)Th and (40)K radionuclides in soil samples were 20±5Bq/kg, 25±10Bq/kg, 25±9Bq/kg and 326±83Bq/kg, respectively. Based on the measurements in this study, the future radiological assessments of other fields in the region should be strategically planned to focus on the oil-sands from the molasses sediments. Disequilibrium in the (228)Ra decay segment was not observed in the soil, sludge or oil-sand samples within the standard uncertainties. After a detailed radiological characterization of the four primary oil fields, we concluded that the outdoor absorbed dose rate never exceeded the worldwide population weighted average absorbed dose rate in outdoor air from terrestrial gamma radiation.

Naturally occurring radioactive materials (NORMs) generated from lignite-fired power plants in Kosovo.

The energy production in Kosovo depends primarily on lignite-fired power plants. During coal combustion, huge amounts of fly ash and bottom ash are generated, which may result in enriched natural radionuclides; therefore, these radionuclides need to be investigated to identify the possible processes that may lead to the radiological exposure of workers and the local population. Lignite samples and NORMs of fly ash and bottom ash generated in lignite-fired power plants in Kosovo are analyzed using a gamma-ray spectrometry method for the activity concentration of natural radionuclides. The average activity concentrations of (40)K, (226)Ra and (232)Th in lignite are found to be 36 ± 8 Bq kg(-1), 9 ± 1 Bq kg(-1) and 9 ± 3 Bq kg(-1), respectively. Indications on the occurrence and geochemical behavior of uranium in the lignite matrix are suggested. The activity concentrations of natural radionuclides in fly ash and bottom ash samples are found to be concentrated from 3 to 5 times that of the feeding lignite. The external gamma-ray absorbed dose rate and the activity concentration index are calculated to assess the radiological hazard arising from ash disposal and recycling in the cement industry.

First characterisation of natural radioactivity in building materials manufactured in Albania.

This study focuses on the radiological characterisation of building materials manufactured in Albania by using a high-resolution gamma-ray spectrometer. The average activity concentrations of (40)K, (226)Ra and (232)Th were, respectively, 644.1±64.2, 33.4 ± 6.4 and 42.2 ± 7.6 Bq kg(-1) in the clay brick samples and 179.7 ± 48.9, 55.0 ± 5.8 and 17.0 ± 3.3 Bq kg(-1) in the cement samples. The calculated activity concentration index (ACI), varied from 0.48±0.02 to 0.63±0.04 in the clay brick samples and from 0.29±0.03 to 0.37±0.02 in the cement samples. Based on the ACI, all of the clay brick and cement samples were categorised as A1 materials. The authors can exclude (at 3σ level) any restriction of their use as bulk materials.

A new FSA approach for in situ γ ray spectroscopy.

An increasing demand of environmental radioactivity monitoring comes both from the scientific community and from the society. This requires accurate, reliable and fast response preferably from portable radiation detectors. Thanks to recent improvements in the technology, γ spectroscopy with sodium iodide scintillators has been proved to be an excellent tool for in-situ measurements for the identification and quantitative determination of γ ray emitting radioisotopes, reducing time and costs. Both for geological and civil purposes not only (40)K, (238)U, and (232)Th have to be measured, but there is also a growing interest to determine the abundances of anthropic elements, like (137)Cs and (131)I, which are used to monitor the effect of nuclear accidents or other human activities. The Full Spectrum Analysis (FSA) approach has been chosen to analyze the γ spectra. The Non Negative Least Square (NNLS) and the energy calibration adjustment have been implemented in this method for the first time in order to correct the intrinsic problem related with the χ(2) minimization which could lead to artifacts and non physical results in the analysis. A new calibration procedure has been developed for the FSA method by using in situ γ spectra instead of calibration pad spectra. Finally, the new method has been validated by acquiring γ spectra with a 10.16 cm × 10.16 cm sodium iodide detector in 80 different sites in the Ombrone basin, in Tuscany. The results from the FSA method have been compared with the laboratory measurements by using HPGe detectors on soil samples collected particular, the (137)Cs isotopes has been implemented in the analysis since it has been found not negligible during the in-situ measurements.