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At least 19 recordsLinked to original sources
PubMed1998

The significance of variations in the angular correction factor in in situ gamma spectrometry.

In situ gamma spectrometry is a powerful method of assessing radioactive contamination in soil. The most widely adopted calibration methodology relates the overall sensitivity of the detector system to the product of three calibration factors: (a) the flux at the detector per unit activity in the ground phi/S(A), (b) the detected count-rate per unit flux incident normally at the detector N0/phi and (c) a correction factor to take into account the angular non-uniformity in response of the detector (Nf/N0). The dependence of the latter factor on the activity distribution with soil depth is generally neglected despite the lack of published evidence to support this. By (i) modelling and (ii) use of published experimental profiles, this work examines the range of Nf/N0 values likely to be encountered in the field. It was found that the use of a fixed angular correction factor is justified given that the maximum errors in the derived activity concentration do not exceed 5% and are far outweighed by other uncertainties.

Calibration↗
PubMed2003

Depth profiling of Pu, 241Am and 137Cs in soils from southern Belarus measured by ICP-MS and alpha and gamma spectrometry.

The depth distribution of plutonium, americium, and 137Cs originating from the 1986 accident at the Chernobyl Nuclear Power Plant (NPP) was investigated in several soil profiles in the vicinity from Belarus. The vertical migration of transuranic elements in soils typical of the 30 km relocation area around Chernobyl NPP was studied using inductively coupled plasma mass spectrometry (ICP-MS), alpha spectrometry, and gamma spectrometry. Transuranic concentrations in upper soil layers ranged from 6 x 10(-12) g g(-1) to 6 x 10(-10) g g(-1) for plutonium and from 1.8 x 10(-13) g g(-1) to 1.6 x 10(-11) g g(-1) for americium. These concentrations correspond to specific activities of (239+240)Pu of 24-2400 Bq kg(-1) and specific activity of 241Am of 23-2000 Bq kg(-1), respectively. Transuranics in turf-podzol soil migrate slowly to the deeper soil layers, thus, 80-95%, of radionuclide inventories were present in the 0-3 cm intervals of turf-podzol soils collected in 1994. In peat-marsh soil migration processes occur more rapidly than in turf-podzol and the maximum concentrations are found beneath the soil surface (down to 3-6 cm). The depth distributions of Pu and Am are essentially identical for a given soil profile. (239+240)Pu/137Cs and 241Am/137Cs activity ratios vary by up to a factor of 5 at some sites while smaller variations in these ratios were observed at a site close to Chernobyl, suggesting that 137Cs is dominantly particle associated close to Chernobyl but volatile species of 137Cs are of relatively greater importance at the distant sites.

Americium↗
PubMed1997

Data quality objectives for surface-soil cleanup operation using in situ gamma spectrometry for concentration measurements.

In situ gamma spectrometry is an efficient method for monitoring the progress of cleanup activities for radioactive contaminants in surface soil and for evaluating the attainment of cleanup standards. However, desired data precision and accuracy must be specified for such a detection system prior to the operation to ensure that the level of uncertainty associated with the concentration measurements is acceptable. A method for developing data quality objectives is described in this paper for in situ gamma spectrometry to achieve numerical goals for data precision and accuracy for cleanup operations. Concentration measurement for a radionuclide at its cleanup level must have a precision commensurate with the importance of cleanup decisions. The 95% lower limit of detection of the system is suggested to be about one tenth the expected system response at the cleanup level. The count time required to achieve the preferred 95% lower limit of detection, and hence the desired precision, can then be determined. The accuracy error arises from the overall calibration factor, which relates the detector responses (e.g., count rate) to physical quantities of interest (e.g., radionuclide soil concentration). The major source of error for the calibration factor using in situ gamma spectrometry is the misidentification of the type of the depth profile of radionuclide concentration in soil. If surrogate radionuclides are used, such as 241Am for plutonium, the variation in the concentration ratio would be another significant source of error. Soil sampling programs performed prior to a cleanup operation will greatly reduce the accuracy error for an in situ detection system, and the analysis of system errors may determine the degree of sampling required. The planning of such a program is discussed in the study. Uncertainty analysis using a Latin Hypercube sampling technique for the calibration factor is also demonstrated. The quantitative result of the uncertainty analysis is useful for determining a nuclide's maximum peak count rate using gamma spectrum that ensures the attainment of the cleanup standard for that nuclide with a pre-specified confidence level (e.g., 95%). The cleanup operation of 239,240Pu in surface soil in the safety shot areas at the Nevada Test Site serves as an example to illustrate the data quality objectives development.

Americium↗
PubMed2000

Low level gamma spectrometry by beta-gamma coincidence

A beta-gamma coincidence system consisting of a 2pi plastic beta detector and a Ge(Li) detector, is described. Such a system allows for a drastic reduction of background (approximately 70 times) as well as of Minimum Detectable Activity (approximately 7 times). An integral background (50-1500 keV) of less than 0.1 cps is obtained. The difficulty of the method, otherwise simple and inexpensive, is the precise determination of beta detector efficiency.

Journal Article↗
PubMed2004

Demonstrating the European capability for airborne gamma spectrometry: results from the eccomags exercise.

Airborne gamma spectrometry (AGS) is being increasingly recognised as an important means for mapping environmental radioactivity in emergency response. Progress has been made in recent years towards methodological convergence and cooperation between European teams. Recently, an international comparison was undertaken in SW Scotland in 2002 to evaluate AGS and ground-based methods. Teams from 18 institutions in 10 European countries attended, collecting some 140,000 AGS spectra, with 750 laboratory gamma spectrometry analyses and 120 in situ observations from the ground sites. Comparisons between AGS and ground-based methods have confirmed the validity of AGS protocols. A composite mapping task, where AGS teams recorded data over adjacent parts of a 90 x 40 km2 area within a few days, confirmed the ability of teams to work together in an effective manner. This paper provides a summary of the results of the exercise. These demonstrate the operational capabilities of European AGS teams and confirm the quantitative nature of the method.

Aircraft↗
PubMed2006

Low-level activity measurement of 131Xem, 133Xem, 135Xe and 133Xe in atmospheric air samples using high-resolution dual X-gamma spectrometry.

High-resolution dual X and gamma spectrometry has been optimized to improve the sensitivity in analyzing radioxenon from environmental samples, especially for the metastable isotopes (131Xem and 133Xem). The full-energy peak (FEP) efficiency curve in the 20-700 keV range has been established with a global uncertainty better than +/-3% using a Monte Carlo simulation. The minimum detectable activity concentrations (MDC) achievable at the laboratory for 131Xem, 133Xem, 133Xe and 135Xe are presented and the influence of 133Xe activity on the metastable radioxenon MDCs is evaluated.

Air Pollutants, Radioactive↗
PubMed2004

Airborne gamma spectrometry--towards integration of European operational capability.

Airborne gamma spectrometry is an excellent tool for finding out in a timely manner the extent and magnitude of the dispersion of radioactive materials resulting from a nuclear disaster. To utilise existing European airborne monitoring capabilities for multilateral assistance in an accident is a complex administrative and technical matter. Several international exercises have been organised demonstrating the capability to cooperate. However, efficient mutual assistance between European countries requires conceptual work, standards and harmonisation of software. A unified radiological vocabulary and data exchange format in XML need to be developed. A comprehensive database is essential for data assimilation. An operations centre is needed for management and planning of surveys.

Aircraft↗
PubMed2004

Radiological maps of outdoor and indoor gamma dose rates in Greek urban areas obtained by in situ gamma spectrometry.

The results obtained from 259 indoor and outdoor in situ gamma spectrometry measurements with a portable Ge detector and 707 total gamma dose rate measurements with an NaI detector in urban areas of 16 Greek islands are presented. From the in situ gamma spectra, the absorbed dose rate in air due to Uranium series, Thorium series, (40)K and (137)Cs are derived and discussed. The results obtained from the present work in conjunction with those reported previously were used for the realization of a complete indoor and outdoor gamma radiation map of Greek urban areas using in situ gamma spectrometry with portable Ge detector.

Air Pollutants, Radioactive↗
PubMed2002

Accounting for the depth distribution of 137Cs in on-line mobile gamma spectrometry through primary and forward-scattered photons.

Stationary and mobile field gamma spectrometry is a useful tool for rapid estimation of environmental radioactivity inventories on and in the ground. A weak point however, is that the depth distribution of the activity in the ground must be known in order to calculate the true activity per unit area or unit mass from an observed photon fluence rate. A promising method for converting incoming spectral data into both true activity content and depth distribution in real time is the peak-to-valley method, which is based on an analysis of the ratio between count rates from primary and forward-scattered photons. In this study the peak-to-valley method was adapted to car-borne mobile gamma spectrometry, where the depth distribution of (137)Cs is fitted to a Lorenz function. Results from field experiments with a large HPGe detector, utilising point sources at different depths, are presented. It was found that the method can be useful for mobile measurements with a measuring time of 5-10 min for activity concentrations of about 100 kBq.m(-2) or higher, resulting in an uncertainty in the estimate of the true activity of about 50%.

Cesium Radioisotopes↗
PubMed2000

Use of gamma-spectrometry for simultaneous determination of 210Pb, 73As, 109Cd, 203Hg and 59Fe distribution and excretion in rats at low doses.

gamma-Spectrometry permits the identification and quantification of different gamma-isotopes in the same aliquot. To estimate the sensitivity and discriminative power of a comparably small and inexpensive 8% germanium detector, we determined the detection limits for simultaneously applied 210Pb, 73As, 109Cd, 203Hg and 59Fe. The concentration of Fe and of each of the four potential environmental contaminants was determined in aliquots from all organs and tissues 10 days after simultaneous i.v. administration (2 micromol/kg body weight) to adult and growing iron-deficient and iron-adequate rats. Relating these values to the total size of each organ permitted to derive a whole body distribution pattern for all five isotopes in each individual animal. Cumulative renal and faecal excretion values were determined during the 10 day distribution period to calculate the half-lives for both excretory pathways for all five isotopes simultaneously. Distribution and excretion values corresponded well to literature data. Extrapolation of the results showed that the detector would be sensitive enough to discriminate and quantify the five metals at human dietary exposure levels. The results recommend to use gamma-spectrometry to investigate kinetic aspects of interactions between toxic and essential trace metals, because the method reduces the number of required animals drastically.

Animals↗
PubMed1989

Measurement of natural radioactivity levels in Indian foodstuffs by gamma spectrometry.

Measurements of natural radioisotopes present in some of the foodstuffs which form the main components of the composite Indian diet are presented. Assessment of daily intake of these natural radionuclides has been made on the basis of the average daily intake of these food-items by the population of Bombay and its environment. The content of 40K, 226Ra and 228Th radioactivity varies from 45.9 to 649.0 Bq/kg, 0.01 to 1.16 Bq/kg and 0.02 to 1.26 Bq/kg, respectively. The average daily intakes of 40K, 226Ra and 228Th have been estimated as 105.6, 0.17 and 0.18 Bq d(-1), respectively for the period 1970-1982.

Eating↗
PubMed2001

Self-absorption correction for gamma spectrometry of powdered milk samples using Marinelli beaker.

Self-absorption was measured for the activity calculation of the 1460.8 and 2614.47 keV lines of the 40K and the 208Tl, respectively, in powdered milk samples. Five Marinelli beakers were prepared with powdered milk in different degrees of compaction and the spectra were measured with an HPGe detector. The detection efficiency versus density was obtained and the self-absorption correction factors versus density were calculated for powdered milk. The results obtained show that this factor must be considered in the calculations of activities.

Animals↗