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Research Articles

Adsorption of Radioactive Iodine Using Nanocarbon on ETS-10 as Adsorbent

, , & ORCID Icon
Pages 1593-1601 | Received 28 Apr 2023, Accepted 07 Mar 2024, Published online: 12 Apr 2024
 

Abstract

Laboratory-synthesized nanocarbon pelletized with titanosilicate (ETS-10) as a support matrix has been investigated for the capture of radioactive iodine present as methyl iodide (CH3I) in the off-gas streams produced during aqueous reprocessing of used nuclear fuel. The mass fraction of carbon in the sorbent matrix was 0.10. The effects of residence time and CH3I concentration were investigated using a continuous flow column setup to quantify the adsorption and desorption capacities of adsorbent under dynamic conditions from an air stream containing CH3I present at concentrations representative of those expected in the off-gas streams. Air with CH3I gas as a source in the column resulted in quantifiable CH3I adsorption with 0.98 mg/g of adsorption capacity. Laboratory-made nanocarbons had a larger adsorption capacity than those of the other carbons reported in the literature. Additionally, the adsorption capacity of nanocarbon on ETS-10 is compared to that of nanocarbon coated on cordierite in previous studies.

Acronyms

AC:=

activated carbon

CH3I:=

methyl iodide

ECD:=

electron capture detector

ETS-10:=

titanosilicate form

GC:=

gas chromatograph

GC-ECD:=

gas chromatograph with electron capture detector

HCNPH:=

hollow carbon nano-polyhedron

ppb:=

parts per billion

SEM:=

scanning electron micropscopy

UHP:=

ultra high purity

UNF:=

used nuclear fuel

VOG:=

vessel off-gas

Nomenclature

Ad ==

adsorption

Cin ==

concentration inlet (mol∙L−1)

Cout ==

concentration outlet (mol∙L−1)

De ==

desorption

Q ==

volumetric flow rate (L∙s−1)

te ==

saturation point (min)

tfinal ==

complete desorption (min)

V ==

volume of reactor (m3)

Greek

τ ==

residence time (ms)

Φ ==

porosity

Disclosure Statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This research work is supported through the U.S. Department of Energy, Office of Nuclear Energy’s Nuclear Energy University Program under [Award DE-NE0008778].

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