One of the most problematic goals for radiation safety during spaceflight is an assessment of additional doses received by astronauts during extravehicular activity (EVA). The Pille-ISS thermoluminescent dosimeter developed by the predecessor of the Hungarian Research Network (HUN-REN) Centre for Energy Research (Budapest, Hungary) is designed for the routine dose measurements not only inside the spacecraft compartments, but also for personal dosimetric control for EVA. During almost two decades of the International Space Station (ISS) operation, the unique set of 131 EVA doses were recorded in different conditions, such as: solar activity, ISS trajectory along the South Atlantic Anomaly (SAA), and shielding conditions provided by two kinds of spacesuits: the Extravehicular Mobility Unit (EMU) and Orlan. The EVA dose rates during the normal scenario (without SAA crossing during EVA) are: 26 μGy/h on average, with maximum value of 118 μGy/h for the EMU spacesuit; and 103 μGy/h on average, with maximum value of 255 μGy/h for the Orlan spacesuit. However, the corresponding EVA dose can increase by about 33% on average regardless the spacesuit type, depending on time spent in SAA. The worst case mean EVA dose is equivalent to ∼ 7 days inside the ISS with 2.423 mGy. In general, the possible additional radiation risk due to the EVA is small in comparison with typical half-year mission onboard the ISS. The long-term experience of EVA dose assessments with Pille-ISS dosimeter shows that in some cases the skin dose can be underestimated due to the excessive shielding of the standard Pille-ISS dosimeter. To solve this problem, the modified Pille-ISS dosimeters with significantly reduced shielding are developed and involved onboard the ISS for the dose measurements starting from 2023.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.lssr.2024.12.005DOI Listing

Publication Analysis

Top Keywords

eva dose
16
dose measurements
12
eva
9
dose
8
pille-iss thermoluminescent
8
thermoluminescent dosimeter
8
μgy/h average
8
average maximum
8
onboard iss
8
pille-iss dosimeter
8

Similar Publications

One of the most problematic goals for radiation safety during spaceflight is an assessment of additional doses received by astronauts during extravehicular activity (EVA). The Pille-ISS thermoluminescent dosimeter developed by the predecessor of the Hungarian Research Network (HUN-REN) Centre for Energy Research (Budapest, Hungary) is designed for the routine dose measurements not only inside the spacecraft compartments, but also for personal dosimetric control for EVA. During almost two decades of the International Space Station (ISS) operation, the unique set of 131 EVA doses were recorded in different conditions, such as: solar activity, ISS trajectory along the South Atlantic Anomaly (SAA), and shielding conditions provided by two kinds of spacesuits: the Extravehicular Mobility Unit (EMU) and Orlan.

View Article and Find Full Text PDF

As the volume of plastic waste from electrical and electronic equipment (WEEE) continues to rise, a significant portion is disposed of in the environment, with only a small fraction being recycled. Both disposal and recycling pose unknown health risks that require immediate attention. Existing knowledge of WEEE plastic toxicity is limited and mostly relies on epidemiological data and association studies, with few insights into the underlying toxicity mechanisms.

View Article and Find Full Text PDF

Indoxyl Sulfate Induces Ventricular Arrhythmias Attenuated by Secretoneurin in Right Ventricular Outflow Tract Cardiomyocytes.

Cardiovasc Toxicol

January 2025

Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, No. 250, Wuxing St., Taipei, 11031, Taiwan.

Ventricular arrhythmias (VAs) are major causes of sudden cardiac death in chronic kidney disease (CKD) patients. Indoxyl sulfate (IS) is one common uremic toxin found in CKD patients. This study investigated whether IS could induce VAs via increasing right ventricular outflow tract (RVOT) arrhythmogenesis.

View Article and Find Full Text PDF

Purpose: To evaluate the efficacy of cenobamate (CNB) in adults with focal epilepsy based on the number of previous lifetime antiseizure medications (ASMs).

Methods: Twenty patients receiving add-on treatment with CNB with <6 lifetime ASMs were retrospectively compared to 20 Patients with >10 ASMs and approximately the same age. Efficacy was assessed at 3, 6, and 12 months following CNB initiation.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!