PubMed Health⌕ Search

PubMed · 8302169

[A solid-state reference sample of iodine radionuclide activity for checking radiometers and a method for its production].

Abstract

This development relates to nuclear engineering, concerns the sources of ionizing radiation of iodine radionuclides and the ways of their manufacture. The iodine radionuclides are used for calibration of radiometers that measure the specific activity of iodine radionuclide in biological specimens, in particular for their use to identify noncancer diseases. The purpose of the paper is to design a routine activity sample for iodine radionuclide in the solid-state source for transfer of an iodine radionuclide activity unit from the reference iodine radionuclide activity unit to an operating meter with a simultaneous decrease in testing errors and an increase, in terms of iodine radionuclide half-life, in the life of the reference sample by stabilizing the activity unit of iodine radionuclide (in terms of its half-life) by eliminating the process of sublimation of iodine radionuclide from the working surface of the source. The objective is achieved by the fact that the radionuclide is replaced on the lower internal build-up part of the container, fixed with the upper internal build-up part, then kept for at least 10-12 hours at least at 18-20 degrees C, packed into a hollow container and sealed with epoxide resin. According to the proposed technical design, reference activity samples of iodine radionuclide in the solid-state radiometric source with a preset activity value have been prepared. The testing error for iodine radionuclide activity is minimal and equal to 1.0-3.0% at a 0.95 confidence.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

G A Sichkar'. [A solid-state reference sample of iodine radionuclide activity for checking radiometers and a method for its production].. https://pubmed.ncbi.nlm.nih.gov/8302169/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Fermentation process tracking through enhanced spectral calibration modeling.

The FDA process analytical technology (PAT) initiative will materialize in a significant increase in the number of installations of spectroscopic instrumentation. However, to attain the greatest benefit from the data generated, there is a need for calibration procedures that extract the maximum information content. For example, in fermentation processes, the interpretation of the resulting spectra is challenging as a consequence of the large number of wavelengths recorded, the underlying correlation structure that is evident between the wavelengths and the impact of the measurement environment. Approaches to the development of calibration models have been based on the application of partial least squares (PLS) either to the full spectral signature or to a subset of wavelengths. This paper presents a new approach to calibration modeling that combines a wavelength selection procedure, spectral window selection (SWS), where windows of wavelengths are automatically selected which are subsequently used as the basis of the calibration model. However, due to the non-uniqueness of the windows selected when the algorithm is executed repeatedly, multiple models are constructed and these are then combined using stacking thereby increasing the robustness of the final calibration model. The methodology is applied to data generated during the monitoring of broth concentrations in an industrial fermentation process from on-line near-infrared (NIR) and mid-infrared (MIR) spectrometers. It is shown that the proposed calibration modeling procedure outperforms traditional calibration procedures, as well as enabling the identification of the critical regions of the spectra with regard to the fermentation process.

Calibration↗

Particle sizing with a fast polar nephelometer.

We reported previously the design of a polar nephelometer that uses a rotational confocal imaging setup to enable fast scanning of the scattering phase function within a field of view of 55 degrees . The full dynamic range of the detection system can be used by increasing the signal-to-noise ratio by means of averaging successive scans. The calibration of the angular response of the instrument is achieved by obtaining the transfer function of the optical detection system using Rayleigh scatterers. Accurate particle sizing of individual polystyrene spheres (ranging from 1.5 to 9 micro m in diameter) in aqueous suspension is achieved by maximizing a correlation coefficient between precalculated tables of Mie phase functions and data obtained from the polar nephelometer. Good correlation is achieved between experimental and theoretical data, proving the functioning of the instrument as a fast and convenient particle sizer.

Calibration↗

Online standard additions calibration of transient signals for inductively coupled plasma mass spectrometry.

An online standard additions calibration method for transient signals in ICPMS is demonstrated in which a small volume of standard is injected as a spike into the sample/carrier stream, overlaying the analyte peak. This technique provides the advantages of conventional standard additions but requires only a single sample run. The method corrects for matrix effects and is suitable for transient signals in which the severity of the matrix effect changes over the analyte peak. The method uses a peak-fitting program to determine the area of the underlying peak and is shown to be effective for the determination of trace metal concentrations in both a high ionic strength matrix and in a biological matrix (urine). Eight analytes with concentrations in the range of 0.82-233.2 mug L-1 in urine were simultaneously determined using a standard spiking solution of 75 mug L-1 injected through a 100-muL loop. The measured concentrations for analytes free of spectral interferences agreed with the certified values, and the precision achieved was comparable to that achieved by the certifying agency. Using a conventional cross-flow nebulizer and Scott-type spray chamber, the accuracy obtained for online standard additions calibration was within 2%, and the precision was within 5%.

Calibration↗