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Characterization technique of gases permeation properties in polymers: H(2), He, N(2) and Ar gas

We demonstrate a simple experimental technology for characterizing the gas permeation properties of H(2), He, N(2) and Ar absorbed in polymers. This is based on the volumetric measurement of released gas and an upgraded diffusion analysis program after high-pressure exposure. Three channel measureme...

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Detalles Bibliográficos
Autores principales: Jung, Jae Kap, Lee, Ji Hun, Jang, Jin Sub, Chung, Nak Kwan, Park, Chang Young, Baek, Un Bong, Nahm, Seung Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885926/
https://www.ncbi.nlm.nih.gov/pubmed/35228634
http://dx.doi.org/10.1038/s41598-022-07321-1
Descripción
Sumario:We demonstrate a simple experimental technology for characterizing the gas permeation properties of H(2), He, N(2) and Ar absorbed in polymers. This is based on the volumetric measurement of released gas and an upgraded diffusion analysis program after high-pressure exposure. Three channel measurements of sorption content of gases emitted from polymers after decompression are simultaneously conducted, and then, the gas uptake/diffusivity as a function of exposed pressure are determined in nitrile butadiene rubber (NBR), ethylene propylene diene monomer (EPDM) rubbers, low-density polyethylene (LDPE) and high-density polyethylene (HDPE), which are used for gas sealing materials under high pressure. The pressure-dependent gas transport behaviors of the four gases are presented and compared. Gas sorption follows Henry’s law up to 9 MPa, while pressure-dependent diffusion behavior is not observed below 6 MPa. The magnitude of the diffusivity of the four gases decreases in the order D(He) > D(H2) > D(Ar) > D(N2) in all polymers, closely related to the kinetic diameter of the gas molecules. The dependence of gas species on solubility is in contrast to that on diffusivity. The linear correlation between logarithmic solubility and critical temperature of the gas molecule was newly observed.