A New Adsorption Rate Equation in Batch Systems

Author(s):  
yongson hong ◽  
Kye-Ryong Sin ◽  
Jong-Su Pak ◽  
Chol-Min Pak

<p><b>In this paper, the deficiencies and cause of previous adsorption kinetic models were revealed, new adsorption rate equation has been proposed and its validities were verified by kinetic analysis of various experimental data.</b> <b>This work is a new view on the adsorption kinetics rather than a comment on the previous adsorption papers.</b></p>

2018 ◽  
Author(s):  
yongson hong ◽  
Kye-Ryong Sin ◽  
Jong-Su Pak ◽  
Chol-Min Pak

<p><b>In this paper, the deficiencies and cause of previous adsorption kinetic models were revealed, new adsorption rate equation has been proposed and its validities were verified by kinetic analysis of various experimental data.</b> <b>This work is a new view on the adsorption kinetics rather than a comment on the previous adsorption papers.</b></p>


2017 ◽  
Author(s):  
yongson hong ◽  
Gwang-Il Kim ◽  
Jin-Xi Zhang ◽  
Chol-Jin Ri ◽  
Gyong-Chol Son ◽  
...  

<p>For many years adsorption kinetics has been investigated, the development of kinetic model has been proceeded in order to obtain the particular kinetic model which better agree with the experimental data. As the result, dozens of kinetic models have been established and used individually despite there are a certain relationship between them. Students often ask which model should be selected to analyze their experimental data among different adsorption kinetic models. In order to clarify dependence relationship and similar degree between adsorption kinetic models, we calculated and compared. Calculation results were successfully compared with the correlation between them and an education method for adsorption kinetic study was proposed. This method can help graduate students of chemical engineering to understand the calculations on kinetics.</p>


2017 ◽  
Author(s):  
yongson hong ◽  
Gwang-Il Kim ◽  
Jin-Xi Zhang ◽  
Chol-Jin Ri ◽  
Gyong-Chol Son ◽  
...  

<p>For many years adsorption kinetics has been investigated, the development of kinetic model has been proceeded in order to obtain the particular kinetic model which better agree with the experimental data. As the result, dozens of kinetic models have been established and used individually despite there are a certain relationship between them. Students often ask which model should be selected to analyze their experimental data among different adsorption kinetic models. In order to clarify dependence relationship and similar degree between adsorption kinetic models, we calculated and compared. Calculation results were successfully compared with the correlation between them and an education method for adsorption kinetic study was proposed. This method can help graduate students of chemical engineering to understand the calculations on kinetics.</p>


1981 ◽  
Vol 46 (13) ◽  
pp. 3247-3263 ◽  
Author(s):  
Jiří Závada ◽  
Magdalena Pánková ◽  
Antonín Vítek

Partial kinetic orders in base for 1-decene, cis-2-decene and trans-2-decene formation from the reaction of 2-decyl bromide with t-C4H9OK in tetrahydrofuran and in tert-butanol and with t-C4H9ONa in tert-butanol have been determined and their significance for assessment of active base has been probed. It has been ascertained that assessment of active base in alkoxide promoted E2 reactions is model-dependent. An unambiguous evidence has been provided by a kinetic analysis of the effect of base concentration on olefin-isomer distribution in the reaction. Two alternative kinetic models of this effect have been devised, the one assuming a competition of several active base species for a single substrate and the other a competition between an uncomplexed and alkoxide-complexed substrate for a single active base. Compatibility of both kinetic models with experimental data has been demonstrated.


2011 ◽  
Vol 332-334 ◽  
pp. 1676-1681
Author(s):  
Hua Zhang ◽  
Tian Ma ◽  
Jie Zhang

In view of the unique porous structure of hemp stem, the comparison experiments were implemented on adsorption properties of hemp stem powder and Abies holophylla Maxim powder to formaldehyde, benzene and TVOC. In addition, on the basis of preliminary study on solid-gas adsorption kinetics of hemp stem, applicability of several adsorption theories was analyzed versus solid-gas adsorption. The results showed that the unique structure endowed hemp stem better adsorption properties than Abies holophylla Maxim’s. However, for different adsorbents, the adsorption kinetics characters differed obviously. Bangham and Langmuir adsorption rate equation fitted the gas-solid adsorption kinetics of hemp stem to some extent, and Langmuir’s could present its absorption to TVOC much better.


2014 ◽  
Vol 809-810 ◽  
pp. 907-911
Author(s):  
Jun Long Wang ◽  
Jie Hou ◽  
Ting Jiang ◽  
Yong Jun He ◽  
Yao Dong Liang

Dry waters with an average diameter of 82 μm were prepared by a high speed mixed route. The formaldehyde absorption kinetics of dry waters was investigated by simulating indoor formaldehyde pollution in glass chamber. The results showed that pseudo-second order model could be used to simulate the adsorption process; the adsorption rate was highest in the initial 60 minutes; when the adsorption lasted for 180 minutes, the adsorption reached equilibrium.


2018 ◽  
Vol 197 ◽  
pp. 09005
Author(s):  
Bregas Siswahjono Tatag Sembodo ◽  
Hary Sulistyo ◽  
Wahyudi Budi Sediawan ◽  
Mohammad Fahrurrozi

Corncobs are potentially processed into bio-oil through thermochemical liquefaction processes. It is difficult to construct kinetics models based on the compounds involved in the reaction. It would be made four kinetic models based on four reaction products, i.e., solids, bio-oil, gas and volatile products. The purposes of the study were to seek kinetics model of thermochemical liquefaction of corncobs in ethanol-water solution and to study the effect of ethanol concentration. The experiment of liquefaction processes of corncobs in ethanol-water solution using sodium carbonate catalyst was performed in the 150 ml autoclave equipped with a magnetic stirrer in the temperature up to 280°C. Four kinetic models were applied to predict the yield of four reaction product lumps. The calculation results were compared to the experimental data. Compared to the others, model 4 was the most realistic and closely matching to the experimental data. In model 4 the reaction mechanism was assumed that biomass (corncobs) first decomposed into bio-oil, followed by decomposition of bio-oil into volatile products reversibly and, finally, volatile products decomposed into gaseous products. The yield of bio-oil increased from 42.05% to 54.93% by increasing to ethanol concentration of 0% to 40%.


2000 ◽  
Vol 65 (7) ◽  
pp. 507-515 ◽  
Author(s):  
Ljubica Vujisic ◽  
Danijela Krstic ◽  
Jovan Vucetic

The influence of Co 2+ ions on the activities of Na+/K+-ATPase and Mg2+ -ATPase, enzymes from rat brain synaptic plasma membrane, was studied. The aim of this study was to investigate the inhibition of both ATPases activities byexposure tocobalt ions as a function of experimentally added CoSO4. The "free" Co2+ concentrations in the reaction mixturewere also calculated and discussed. CoSO4 induced a dose-dependent inhibition of both enzymes. The IC50 values of Co 2+, as calculated from the experimental curves, were 168 mM for Na+/K+-ATPase and 262 mMfor Mg 2+-ATPase, and for the recalculated free Co 2+ concentration 75.4 mM for Na+/K+-ATPase and 136 mM for Mg 2+-ATPase. The obtained linear Dixon's plot for Na+/K+-ATPase implies equilibium binding of cobalt with inhibitory sites on the enzyme. The kinetic parameters for both enzymes in presence and absence of CoSO4 were calculated from the experimental data. The results of the kinetic analysis show that inhibition of Na+/K+-ATPase induced by CoSO4 is non-competitive, and for Mg 2+-ATPase that there are two sites of different sensitivities or two different enzymes.


2021 ◽  
Author(s):  
khaled Mostafa ◽  
H. Ameen ◽  
A. Ebessy ◽  
A. El-Sanabary

Abstract Our recently tailored and fully characterized poly (AN)-starch nanoparticle graft copolymer having 60.1 G.Y. % was used as a starting substrate for copper ions removal from waste water effluent after chemical modification with hydroxyl amine via oximation reaction. This was done to change the abundant nitrile groups in the above copolymer into amidoxime one and the resultant poly (amidoxime) resin was used as adsorbent for copper ions. The resin was characterized qualitatively via rapid vanadium ion test and instrumentally by FT-IR spectra and SEM morphological analysis to confirm the presence of amidoxime groups. The adsorption capacity of the resin was done using the batch technique, whereas the residual copper ions content in the filtrate before and after adsorption was measured using atomic adsorption spectrometry. It was found that the maximum adsorption capacity of poly (amidoxime) resin was 115.2 mg/g at pH 7, 400ppm copper ions concentration and 0.25 g adsorbent at room temperature. The adsorption, kinetics and isothermal study of the process is scrutinized using different variables, such as pH, contact time, copper ion concentration and adsorbent dosage. Different kinetics models comprising the pseudo-first-order and pseudo-second-order have been applied to the experimental data to envisage the adsorption kinetics. It was found from kinetic study that pseudo-second-order rate equation was better than pseudo-first-order supporting the formation of chemisorption process. While, in case of isothermal study, the examination of calculated correlation coefficient (R2) values showed that the Langmuir model provide the best fit to experimental data than Freundlich one.


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