Abstract

The number and strength of adsorption sites for Xe in silver-modified zeolites are estimated from isotherm measurements at various temperatures over a broad range of pressure (from 1 ppm to atmospheric pressure). Fully and partially exchanged silver zeolites were synthesized starting from Na-ZSM-5(25), Na-ZSM-5(40), Na-Beta, NaX, and NaY. We have discovered that silver-modified zeolites may present one or two distinct adsorption sites depending on the nature of the material and silver loadings. The strongest adsorption sites are characterized by isosteric heat of adsorption in the order of −40 to −50 kJ·mol–1. For Pentasil-type zeolites, we observe a linear 2:1 correlation between the total amount of silver and the number of strong sites. The highest concentration of strong sites is found for fully silver exchanged ZSM-5 (5.7 × 10–4 mol/g), which presents the largest silver content for Pentasil-type zeolite. The equilibrium constant of Ag-ZSM-5 at low pressure is about 50 times larger than that of AgX. Qualitative correlations were established between Xe adsorption isotherms and Xe NMR signals. We show that Xe NMR could be used as a quantitative method for the characterization of the strength and of the number of strong Xe adsorption sites on silver-exchanged zeolites. The numbers of strong adsorption sites responsible for the Xe adsorption at 10–1000 ppm can be determined by the length of the plateau observed at low Xe uptake. In practice, our findings give guidelines for the discovery and optimization of silver-loaded zeolites for the capture of Xe at ppm levels. It appears that the amount of silver is a key parameter. Silver-modified ZSM-5 shows adsorption capacities 2–3 orders of magnitude larger than currently applied adsorbents for atmospheric Xe capture.

Highlights

  • At large, xenon is currently extracted from air by distillation

  • The monitoring of radioactive xenon isotopes in the atmosphere is continuously performed at different places worldwide in application of the verification regime of the Comprehensive Nuclear Test Ban Treaty (CTBT).[2−7] In a nuclear explosion, four radioactive xenon isotopes are produced in significant amounts with halflives long enough for them to be detected even several days after the explosion: 131mXe (t1/2 = 11:84 d), 133Xe (t1/2 = 5:243 d), 133mXe (t1/2 = 2:19 d), 135Xe (t1/2 = 9:14 h)

  • The results prove that the large signals observed in the case of AgX are due to the presence of several overlapping isotropic signals, since they are not changing under magic angle spinning

Read more

Summary

Introduction

Xenon is currently extracted from air by distillation. Most of the xenon produced in the world is used in specialized lighting.[1]. The modeling of isotherms allows discriminating two types of adsorption sites depending on the nature of zeolites (pentasil versus faujasite) and silver loading.

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