On the basis of the flow study presented in Part I the desorption behaviour of the isobaric laboratory adsorber is investigated. The investigation is suitable to identify the micropore diffusion mechanism of NH3 molecules in A-type zeolite crystals. The sorption system is characterized by the fact t
Concentration-dependent micropore diffusion analysed by measuring laboratory adsorber dynamics—I. Study of the adsorber flow behaviour
✍ Scribed by R. Gutsche
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 758 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0009-2509
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✦ Synopsis
The flow behaviour of an isobaric laboratory adsorber is investigated. This investigation is the basis for a correct analysis of the concentration-dependent micropore diffusion as presented in Part II. Exit functions of the inactive adsorber (containing sorption inert particles) were measured as the response to non-ideal step functions. The experimental exit functions are well fitted by the dispersion as well as the series-of-stirred-tanks (SST) model. However, only the more time-consuming dispersion model is found to describe the real local mixing characteristics of the adsorber. This property of the flow model is necessary because the non-linear sorption dynamics are highly sensitive to variations in the local mixing states, even if these variations do not affect the exit function (residence-time distribution) of the inactive adsorber. A computation study reveals that this sensitivity is repealed by (I) measuring desorption (instead of adsorption) behaviour and (2) utilizing the short-bed technique. By implementing the latter conditions it is possible to use the simple and computer time-sparing SST model for the correct determination of the non-linear micropore diffusion mechanism.
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