Role of catalyst pellet activity distribution in catalyst poisoning

1994 ◽  
Vol 108 (2) ◽  
pp. 141-156
Author(s):  
Alena Brunovská ◽  
Bibiána Remiarová ◽  
Pavol Pranda
2007 ◽  
Vol 145 (3) ◽  
pp. 786-800 ◽  
Author(s):  
Klaus von Schwartzenberg ◽  
Marta Fernández Núñez ◽  
Hanna Blaschke ◽  
Petre I. Dobrev ◽  
Ondrej Novák ◽  
...  

1987 ◽  
Vol 52 (10) ◽  
pp. 2426-2437 ◽  
Author(s):  
Alena Brunovská ◽  
Josef Horák

In this paper a method of simultaneous estimation of the catalyst pellet activity distribution, the mean reaction rate constant, and the diffusion coefficient from kinetic data is described. As kinetic data measurements of outlet concentration from laboratory continuous stirred tank reactor vs feed rate for zero order reaction is used. The estimation technique is verified on simulated data. The mean reaction rate constant is estimated from the region of investigated dependence in which reactant penetrates into the whole catalyst pellet. The value of the effective diffusion coefficient and the activity distribution are estimated from the regime in which the reactant penetrates into the part of the pellet only.


1973 ◽  
Vol 134 (2) ◽  
pp. 387-398 ◽  
Author(s):  
Michael Norman ◽  
Stjepan Gamulin ◽  
Kay Clark

1. To investigate the role of ribosome function in regulating protein synthesis, the activity, distribution and functional states of ribosomal particles were investigated in livers of mice fed ad libitum or starved overnight. 2. The distribution of protein-synthesizing activity between polyribosomes of different sizes was analysed after incorporation of radioactive leucine, and the quantitative distribution of ribosomes as native subunits, monomers and polyribosomes was analysed after incorporation of orotic acid. Precursors labelled with 3H or 14C were given separately to fed and starved mice, so that livers from the two groups of animals were processed together. 3. The former experiments showed that starvation has little effect on the distribution of protein-synthesizing activity across polyribosome sedimentation patterns, though the latter experiments showed that the proportion of ribosomes existing as monomers increased from 9.5% to 15.2%, whereas the proportion existing as polyribosomes decreased from 81.4% to 75.6%. Starvation had a negligible effect on the proportion of native subunits, which accounted for 9.1% and 9.2% of the ribosomes in fed and starved mice respectively. 4. The monomeric ribosome fraction was isolated and subjected to ionic conditions which selectively dissociate single ribosomes. Starvation increased the proportion of monomers that dissociated from 59% to 72%, so the monomers that accumulate in livers of starved animals are single ribosomes and not monoribosomes resulting from degradation of polyribosomes. 5. The fate of newly formed ribosomal particles was studied by measuring the specific radioactivity of native subunits, monomers and polyribosomes at different times after injection of radioactively labelled orotic acid. Starvation did not appear to affect equilibration between newly formed particles and polyribosomes, and the radioactivity of polyribosomes in both groups of mice reached about 90% of that in native subunits after 4h. The radioactive labelling of monomers proceeded at a slower rate, especially after starvation. At 4h, the radioactivity of monomers was 64% and 55% that of native subunits in fed and starved mice respectively.


1989 ◽  
Vol 54 (2) ◽  
pp. 388-399 ◽  
Author(s):  
Alena Brunovská ◽  
Bibiana Remiarová ◽  
Carlo Lebrun

In this paper a method of catalyst pellet activity distribution estimation from experimental kinetic data is described. Measurements of outlet concentration from a laboratory continuous stirred single-pellet reactor vs feed rate for ethylene hydrogenation on Pt/alumina pellet are used as kinetic data. To find the best estimate the gradient method is employed and the gradient is computed with the help of the adjoint equation. The estimated activity distribution is compared with the Pt distribution obtained by the scanning electron microscope.


1986 ◽  
Vol 165 (2-3) ◽  
pp. L80-L84 ◽  
Author(s):  
J.M. MacLaren ◽  
J.P. Pendry ◽  
R.W. Joyner
Keyword(s):  

1983 ◽  
Vol 38 (12) ◽  
pp. 1977-1982 ◽  
Author(s):  
A.L. Cukierman ◽  
M.A. Laborde ◽  
N.O. Lemcoff

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