Sorption and Transport of Species in Silicalite Study of Binary Systems Containing Iodine

1998 ◽  
Vol 63 (3) ◽  
pp. 321-337 ◽  
Author(s):  
Vladimír Masařík ◽  
Pavel Novák ◽  
Arlette Zikánová ◽  
Jan Kornatowski ◽  
Jaroslav Maixner ◽  
...  

Sorption of iodine from both the vapour phase and iodine solutions in organic solvents on large Silicalite-1 crystals was investigated. The single component sorption of iodine and sorption from binary mixtures under co-diffusion conditions led to a uniform colouring of the crystals. Under counter-diffusion conditions with crystals saturated initially with vapour of a selected solvent, the sorption kinetics of iodine was 2 or 3 orders of magnitude slower as compared with the corresponding co-diffusion experiment. Colouring of crystals was always, at least in its initial stage, non-uniform with visualized pyramids at crystal basal planes. This finding together with the nature of outer and inner crystal morphology suggests that our Silicalite-1 crystals are 90°-intergrowths which have only pore mouth openings of sinusoidal channels in the crystal surface. The process of crystal colouring under counter-diffusion conditions seems to proceed via diffusion along the boundaries of crystal sections.

1994 ◽  
Vol 59 (7) ◽  
pp. 1525-1535 ◽  
Author(s):  
André Micke ◽  
Peter Struve ◽  
Martin Bülow ◽  
Milan Kočiřík ◽  
Arlette Zikánová

Adsorption equilibrium and sorption uptake data have been measured for the system p-ethyltoluene/NaH-ZSM-5 zeolite under constant volume/variable pressure condition at elevated ambient temperature of 343 K. The equilibrium data are described by a superposition of two Langmuir isotherms. The uptake curves observed in the present paper revealed devations from the second Fick law behaviour. The experimental uptake curves are compatible with rate mechanism involving Fickian diffusion superimposed by a surface barrier. The evaluation of the model parameters was carried out by simulation of the kinetic curves that include both the interactions of the system with the apparatus and the intrinsic sorption kinetics. The dependence of the fitted model parameters on sorbent amount and pressure, respectively, is consistent with Langmuir sorption kinetics at crystal surface on one side and with the concept of molecule jumps on a system of fixed positions in the crystal bulk on the other.


2015 ◽  
Vol 77 (5) ◽  
pp. 608-613 ◽  
Author(s):  
E. P. Yelsukov ◽  
D. A. Kolodkin ◽  
I. A. El’kin ◽  
A. L. Ul’yanov ◽  
V. E. Porsev

1979 ◽  
Vol 44 (4) ◽  
pp. 1187-1196 ◽  
Author(s):  
Ivona Malijevská

The relations were obtained between the thermodynamically consistent activity coefficient of associating component and the activity coefficient calculated irrespective of the association in the vapour phase. The analysis is limited to binary systems with one associating component and is given for the two cases: (a) the associating component dimerizes only, (b) the associating component forms, in addition to a dimer, one higher associate, too.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Veniamin Zheleznov ◽  
Aleksey Golikov ◽  
Tatiana Sokolnitskaya ◽  
Sergey Ivannikov

Abstract The sorption kinetics of uranyl ions micro-quantities from fluoride solutions by nanostructured materials with anatase mesoporous structures has been studied. Using the model of competitive sorption of ions and positively charged complexes of uranyl ion on deprotonated hydroxyl groups of an anatase, kinetic curves of changes in the ratio of ionic forms of uranium in solution were calculated. Modeling was carried out under the assumption of a two-stage mechanism of uranium complex ions sorption. The modeling considered the influence of the uranyl ion carbonate complexes formation. The shift in equilibrium among ionic forms of uranyl correlates with the stability of the complexes in solution.


1991 ◽  
Vol 69 (12) ◽  
pp. 2018-2023 ◽  
Author(s):  
Refat M. Hassan

The kinetics of permanganate oxidation of DL-α-alanine in aqueous perchloric acid solution at a constant ionic strength of 2.0 mol dm−3 has been investigated spectrophotometrically. The reaction was found to show second-order kinetics overall with respect to each of the reactants in the slow initial stage; the second-order kinetics are not, however, maintained throughout the relatively fast final stage of reaction. The added salts lead to the prediction that Mn(III) and (or) Mn(IV) play a very important role in the reaction kinetics. A tentative mechanism consistent with the kinetics is discussed. Key words: kinetics, oxidation, reduction, amino acids, permanganate.


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