The recent release of contaminated water from the Fukushima Daiichi Nuclear Power Plant highlights the need for accurate tritium measurement, particularly near the minimum detectable activity (MDA) of 5 Bq·L−1 set by South Korea’s Nuclear Safety and Security Commission. This study aims to improve low-level tritium measurement accuracy by optimizing the region of interest (ROI) for quench curve determination. These adjustments are crucial for separating tritium signals from background noise. Quench standards were prepared and measured using a liquid scintillation counter (LSC). Three ROIs were analyzed to assess the impact of channel selection on measurement precision: A 20-148 channel range optimized via figure of merit (FOM) analysis, a 20-250 channel range covering tritium’s full beta spectrum, and a broad 1-1024 channel range. Quench curves were obtained by fitting the counting efficiency of each ROI to the quench standards. Tritium samples with six different activity levels were prepared, and their radioactivity was calculated using the quench curves. Selecting appropriate ROIs for quench curve determination is critical for measuring low-concentration tritium accurately. This approach reduces uncertainty and emphasizes reliable methods to improve the precision and consistency of tritium measurements.

Breakthrough analysis has widely been explored for the dynamic separation of gaseous mixtures in porous materials. In general, breakthrough experiments measure the components of a flowing gas when a gaseous mixture is injected into a column filled with an adsorbent material. In this paper, we report on the design and fabrication of a breakthrough curve measurement device to study the dynamic adsorptive separation of hydrogen isotopologues in porous materials. Using the designed system, an experiment was conducted involving a 1:1 mixture of hydrogen and deuterium passed through a column filled with zeolite 13X (1 g). At room temperature, both hydrogen and deuterium were adsorbed in negligible amounts; however, at a temperature of 77 K, deuterium was preferentially adsorbed over hydrogen. The selectivity was different from that in the existing literature due to the different sample shapes, measurement methods, and column structures, but was at a similar level to that of cryogenic distillation (1.5).