Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine · 2026
The equivalent volume method for gamma spectrometry calibration: A new method bridging the gap between distributed and point sources.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Eadan Z A, Al-Motawakel M K
Аннотация
The high cost and limited availability of standard reference materials often restrict customized efficiency calibration in gamma spectrometry. This study introduces the Equivalent Volume Method (EQVM), a calibration approach that reduces dependence on such standard materials by using point sources together with a physically defined "Equivalent Volume" to generate efficiency curves directly within Genie 2000 software. Systematic experiments were conducted using various environmental matrices with densities ranging from 0.44 to 1.6 g/cm3 and multiple cylindrical geometries. A consistent linear correlation was observed between the spiked sample volume and the equivalent volume, defined by a constant scaling factor (F≈0.35±0.02), independent of gamma energy, density, and matrix composition. A similar proportionality was observed between self-absorption and linear attenuation coefficients, supporting the physical basis of the method. Four theoretical models were derived, supporting the experimental findings and introducing a critical point value as a physics criterion used for validating efficiency correction models. Validation against spiked samples and IAEA-certified reference material showed agreement within 1.5% relative deviation. The EQVM provides a precise, flexible, and economically superior alternative to the gamma spectrometry calibration, enabling customized calibration and accurate activity determination without requiring matrix-specific corrections over the studied range.