Abstract

An activated carbon prepared from silicon carbide by thermochemical synthesis and designated as SiC-AC was studied as an adsorbent for xenon. The examination of textural properties of the SiC-AC adsorbent by nitrogen vapor adsorption measurements at 77 K, powder X-ray diffraction, and scanning electron microscopy revealed a relatively homogeneous microporous structure, a low content of heteroatoms, and an absence of evident transport macropores. The study of xenon adsorption and adsorption-induced deformation of the Si-AC adsorbent over the temperature range of 178 to 393 K and pressures up to 6 MPa disclosed the contraction of the material up to −0.01%, followed by its expansion up to 0.49%. The data on temperature-induced deformation of Si-AC measured within the 260 to 575 K range was approximated by a linear function with a thermal expansion factor of (3 ± 0.15) × 10−6 K−1. These findings of the SiC-AC non-inertness taken together with the non-ideality of an equilibrium xenon gaseous phase allowed us to make accurate calculations of the differential isosteric heats of adsorption, entropy, enthalpy, and heat capacity of the Xe/SiC-AC adsorption system from the experimental adsorption data over the temperature range from 178 to 393 K and pressures up to 6 MPa. The variations in the thermodynamic state functions of the Xe/SiC-AC adsorption system with temperature and amount of adsorbed Xe were attributed to the transitions in the state of the adsorbate in the micropores of SiC-AC from the bound state near the high-energy adsorption sites to the molecular associates.

Highlights

  • Xenon is the least abundant of the noble gas family of elements

  • We examined the factors affecting the xenon adsorption performance of a carbon adsorbent prepared from silicon carbide, SiC-activated carbons (ACs)

  • The carbon adsorbent prepared from silicon carbide, SiC-AC, was examined to view the potential application for adsorption-based storage of xenon

Read more

Summary

Introduction

Xenon is the least abundant of the noble gas family of elements. It is found in trace amounts in the Earth’s atmosphere (8.6 × 10−5 vol %) and as a component of gases evolved from mineral springs [1,2]. Xenon is obtained in industrial-scale volumes as an air separation by-product at the large-scale production of liquid oxygen at metallurgical plants [3]. On a much smaller scale, xenon and krypton are emitted as fusion products of uranium dioxide used as fuel for reactors at the existing nuclear power plants (NPP). The fission gases are dominated by Xe and Kr, which exist in the form of approximately 20 isotopes. The relative amounts of the xenon isotopes are somewhat dependent upon the kind of reactor. In some types of nuclear reactors, it is necessary to remove 135 Xe from the cooling gas for reasons of neutron economy since 135 Xe has a very large neutron capture

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call