Abstract

In this work, the 222^{222}Rn contamination mechanisms on acrylic surfaces have been investigated. 222^{222}Rn can represent a significant background source for low-background experiments, and acrylic is a suitable material for detector design thanks to its purity and transparency. Four acrylic samples have been exposed to a 222^{222}Rn rich environment for different time periods, being contaminated by 222^{222}Rn and its progenies. Subsequently, the time evolution of radiocontaminants activity on the samples has been evaluated with α\alpha and γ\gamma measurements, highlighting the role of different decay modes in the contamination process. A detailed analysis of the alpha spectra allowed to quantify the implantation depth of the contaminants. Moreover, a study of both α\alpha and γ\gamma measurements pointed out the 222^{222}Rn diffusion inside the samples

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