In recent years, optical fibers have found extensive use in special environments, including high-energy radiation scenarios like nuclear explosion diagnostics and reactor monitoring. However, radiation exposure, such as X-rays, gamma rays, and neutrons, can compromise fiber safety and reliability. Consequently, researchers worldwide are focusing on radiation-resistant fiber optic technology. This paper examines optical fiber radiation damage mechanisms, encompassing ionization damage, displacement damage, and defect centers. It also surveys the current research on radiation-resistant fiber optic design, including doping and manufacturing process improvements. Ultimately, it summarizes the effectiveness of various approaches and forecasts the future of radiation-resistant optical fibers.

Recent advancements in tritium separation technologies have significantly improved efficiency, particularly through the integration of vapor phase catalytic exchange (VPCE), liquid phase catalytic exchange (LPCE), and combined electrolysis catalytic exchange (CECE) methods. Combining these techniques overcomes individual limitations, enhancing separation efficiency and reducing energy consumption. The CECE process, which integrates electrolysis with catalytic exchange, offers high separation factors, making it effective for high-concentration tritiated water treatment. Solid polymer electrolyte (SPE) technology has also gained prominence for its higher efficiency, smaller equipment size, and longer lifespan compared to traditional alkaline electrolysis. While electrolysis offers high separation factors, its high energy demand limits its cost-effectiveness for large-scale operations. As a result, electrolysis is often combined with other methods like CECE to optimize both energy consumption and separation efficiency. Future research will focus on improving the energy efficiency of electrolysis for large-scale, low-cost tritiated water treatment.

Iodine is one of the key elements that must be removed from the off-gas systems of nuclear fuel reprocessing. This study systematically investigates the iodine vapor adsorption performance of the metal–organic framework (MOF) material HKUST-1(1-(2-methyl-4-(2-oxopyrrolidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one), with particle sizes of 100 nm and 20 μm. HKUST-1 samples with varying particle sizes were synthesized via a hydrothermal method. The experimental results show that the 20 μm HKUST-1 exhibits superior crystallinity, a more intact pore structure, and a higher iodine adsorption capacity, reaching 700 mg/g, which is significantly greater than the 300 mg/g capacity of the 100 nm HKUST-1. Kinetic analysis reveals that the adsorption process follows the pseudo-second-order model, with physical adsorption as the predominant mechanism, where iodine molecules are accommodated within the pores. FTIR and XRD further confirm the structural stability of the HKUST-1 framework after iodine adsorption. However, desorption experiments show that iodine molecules are easily volatilized into the air, with a 20% weight loss observed within 10 h and a color change from black to green. The results provide experimental evidence for optimizing the application of HKUST-1 materials in iodine capture and suggest that material modification could enhance the long-term stability of iodine fixation.

Three phenylpyridine diamide ligands displayed high selectivity for Pu(iv) over other metals in a HNO₃ medium. They also demonstrated good stripping ability and reusability, with reasonable radiolytic stability up to an absorbed dose of 100 kGy.

The separation of palladium from radioactive waste streams represents a critical aspect of the secure handling and disposal of such hazardous materials. Palladium, in addition to its radioactive nature, holds intrinsic value as a resource. Despite the urgency, prevailing adsorbents fall short in their ability to effectively separate palladium under highly acidic environments. To surmount this challenge, our research has pioneered the development of 1,3,5-tris(4-aminophenyl)benzene-2,5-Bis(methylthio)terephthalaldehyde COF (TAPB-BMTTPA-COF), a novel material distinguished by its remarkable stability and an abundance of sulfur-containing functional groups. Leveraging the pronounced affinity of the soft ligands’ nitrogen and sulfur within its molecular architecture, TAPB-BMTTPA-COF demonstrates an exceptional capability for the selective adsorption of palladium. Empirical evidence underscores the material’s swift adsorption kinetics, with equilibrium achieved in as little as ten minutes, and its broad tolerance to varying acidity levels ranging from 0.1 to 3 M HNO₃. Furthermore, TAPB-BMTTPA-COF boasts an impressive adsorption capacity, peaking at 343.6 mg/g, coupled with high selectivity in 13 interfering ions’ environment and the ability to be regenerated, making it a sustainable solution. Comprehensive analyses, including Fourier Transform Infrared Spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS), alongside Density Functional Theory (DFT) calculations, have corroborated the pivotal role played by densely packed nitrogen and sulfur active sites within the framework. These sites exhibit a robust affinity for Pd(II), which is the cornerstone of the material’s outstanding adsorption efficacy. The outcomes of this research underscore the immense potential of COFs endowed with resilient linkers and precisely engineered functional groups. Such COFs can adeptly capture metal ions with high selectivity, even in the face of severe environmental conditions, thereby paving the way for the more effective and environmentally responsible management of radioactive waste.