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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 A computation study reveals that this sensitivity is repealed by (I) measuring desorption (instead of adsorption) behaviour and (2) utilizing the short-bed technique.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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Concentration-dependent micropore diffus
✍ R. Gutsche 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 608 KB

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