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The multichannel analyzer (MCA) is a crucial device for recording and analyzing radiation energy spectra to ascertain energy and intensity. It can be implemented via FPGA with a fast ADC and digital algorithm or a microcontroller with a peak detector circuit using an analog electrical circuit. MCA is widely applied in field work, nuclear medicine, and accelerator experiments. This work focuses on developing a lowcost alpha and gamma spectrometric system for experimental physics and field work, such as recording radiation and monitoring nuclear facility surroundings. Modern microcircuits, with small size and low power consumption, enable simpler and cheaper analog signal processing circuits that process signals in real-time without digital conversion delays. The spectrometric amplifier (SA) and peak detector (PD) were modeled and prototyped. A Python-based real-time data acquisition program was developed. Signals are recorded on the STM32F407 microcontroller’s ADC and transmitted via USB to a PC. An experiment obtaining the Ra226 alpha source spectrum verified the MCA’s functionality. It is valuable for environmental radioactivity field work and student teaching.

This paper presents the results of 4 reactor campaigns on the irradiation of biphasic lithium ceramics containing different ratios of lithium orthosilicate (LOS) and lithium metatitanate (LMT) components (25 and 35 mol% LMT in LOS). The size distribution of pebbles in pebble beds was 250–1250 μm and 500–710 μm, respectively. The studies were carried out sequentially with each type of ceramics. In experiments carried out using the vacuum extraction method, the composition of gases released from lithium ceramic samples was registered in in-situ mode. The absence of purge gas during the experiments minimized the possibility of T2O and HTO formation, significantly simplifying processing of the results and providing more opportunities for results analysis. The main goal of the present paper was to identify the general patterns of the release of gases with mass numbers M2 (H2), M4 (He + HT), M6 (T2) and M18 (H2O) from ceramic samples throughout the entire irradiation experiment in 4 campaigns. Release trends of main gases with mass numbers M2, M4, M6 and M18 for all four campaigns are presented and their comparative analysis was performed. The average partial pressure of tritium release in the form of T2 and HT molecules for all campaigns was determined as 5.8 × 10-7 Torr. The dependences of formation rates of helium release peaks on the irradiation time were plotted. The nature of peak emissions does not have a monotonic relationship; upon irradiation, both an increase in the frequency of peaks and a decrease in it are observed. During irradiation, the process of peak helium release does not stop.The simulation was carried out by the finite element method, assuming that tritium release from the sample is determined by diffusion and desorption processes from the sample surface. The experimental curves are satisfactorily described by a number of sets of desorption and diffusion parameters. One way or another they lie in the range of specified values. The Arrhenius dependences of the effective diffusion coefficient and desorption coefficient obtained for lithium ceramics 35 LMT are equal to:D=5,2×10-11m2sexp-21kJmoleRT,K=1.21×10-4m2sexp-64kJmoleRT.The values of the effective diffusion coefficient and tritium desorption coefficient in 25 LMT ceramics were 15 and 20% lower than in 35 LMT ceramics.