Diffusion Coefficient and Reaction Rate Constant of the SiH3Radical in Silane Plasma

1989 ◽  
Vol 28 (Part 2, No. 2) ◽  
pp. L325-L328 ◽  
Author(s):  
Naoshi Itabashi ◽  
Kozo Kato ◽  
Nobuki Nishiwaki ◽  
Toshio Goto ◽  
Chikashi Yamada ◽  
...  

The paper presents an analytical solution for the dispersion of a solute in a liquid flowing between two parallel plates in the presence of an irreversible first-order chemical reaction. The effects of both homogeneous and heterogeneous reactions on the dispersion are studied under isothermal conditions. It is found that for homogeneous reaction in the bulk of the liquid, the effective Taylor diffusion coefficient decreases with increase in the reaction rate constant. Further for heterogeneous reaction at the catalytic walls, Taylor diffusion coefficient is also found to decrease with increase in the wall catalytic parameter for fixed reaction rate constant corresponding to the bulk reaction.


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.


1994 ◽  
Vol 27 (8) ◽  
pp. 1660-1663 ◽  
Author(s):  
T Tanaka ◽  
M Hiramatsu ◽  
M Nawata ◽  
A Kono ◽  
T Goto

2019 ◽  
Vol 292 ◽  
pp. 01063
Author(s):  
Lubomír Macků

An alternative method of determining exothermic reactor model parameters which include first order reaction rate constant is described in this paper. The method is based on known in reactor temperature development and is suitable for processes with changing quality of input substances. This method allows us to evaluate the reaction substances composition change and is also capable of the reaction rate constant (parameters of the Arrhenius equation) determination. Method can be used in exothermic batch or semi- batch reactors running processes based on the first order reaction. An example of such process is given here and the problem is shown on its mathematical model with the help of simulations.


2007 ◽  
Vol 544-545 ◽  
pp. 95-98 ◽  
Author(s):  
Jong Tae Jung ◽  
Jong Oh Kim ◽  
Won Youl Choi

The purpose of this study is to investigate the effect of the operational parameters of the UV intensity and TiO2 dosage for the removal of humic acid and heavy metals. It also evaluated the applicability of hollow fiber microfiltration for the separation of TiO2 particles in photocatalytic microfiltration systems. TiO2 powder P-25 Degussa and hollow fiber microfiltration with a 0.4 μm nominal pore size were used for experiments. Under the conditions of pH 7 and a TiO2 dosage 0.3 g/L, the reaction rate constant (k) for humic acid and heavy metals increased with an increase of the UV intensity in each process. For the UV/TiO2/MF process, the reaction rate constant (k) for humic acid and Cu, with the exception of Cr in a low range of UV intensity, was higher compared to that of UV/TiO2 due to the adsorption of the membrane surface. The reaction rate constant (k) increased as the TiO2 dosage increased in the range of 0.1~0.3 g/L. However it decreased for a concentration over 0.3 g/L of TiO2. For the UV/TiO2/MF process, TiO2 particles could be effectively separated from treated water via membrane rejection. The average removal efficiency for humic acid and heavy metals during the operational time was over 90 %. Therefore, photocatalysis with a membrane is believed to be a viable process for humic acid and heavy metals removal.


1990 ◽  
Vol 95 (D9) ◽  
pp. 13981 ◽  
Author(s):  
Gaunlin Shen ◽  
Masako Suto ◽  
L. C. Lee

Author(s):  
Shigenori Togashi ◽  
Yukako Asano ◽  
Yoshishige Endo

The chemical reaction yield was predicted by using Monte Carlo simulation. The targeted chemical reaction of a performance evaluation using the microreactor is the consecutive reaction. The main product P1 is formed in the first stage with the reaction rate constant k1. Moreover, the byproduct P2 is formed in the second stage with the reaction rate constant k2. It was found that the yield of main product P1 was improved by using a microreactor when the ratio of the reaction rate constants became k1/k2 >1. To evaluate the Monte Carlo simulation result, the yields of the main products obtained in three consecutive reactions. It was found that the yield of the main product in cased of k1/k2 >1 increased when the microreactor was uesd. Next, a pilot plant involving the numbering-up of 20 microreactors was developed. The 20 microreactor units were stacked in four sets, each containing five microreactor units arranged. The maximum flow rate when 20 microreactors were used was 1 × 104 mm3/s, which corresponds to 72 t/year. Evaluation of the chemical performance of the pilot plant was conducted using a nitration reaction. The pilot plant was found to capable of increasing the production scale without decreasing the yield of the products.


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