scholarly journals Translocation of Cations During Sorption of Copper in the System Solution - Algae (Spirogyra sp.)/Translokacja Kationów Podczas Procesu Sorpcji Miedzi W Układzie Roztwór - Glony (Spirogyra Sp.)

2014 ◽  
Vol 21 (3) ◽  
pp. 425-433
Author(s):  
Małgorzata Rajfur ◽  
Andrzej Kłos ◽  
Jan Kříž

Abstract Kinetics of the sorption of copper cations in Spirogyra sp. algae was analysed, together with the accompanying processes of hydrogen cations sorption and releasing to the solution the cations bonded in the algae: Na+, Mg2+, K+ and Ca2+. It was established that, in a static system, at the fixed proportion of algae mass to the solution volume, these processes occur simultaneously, however presumably the quantity of the released salts influences the parameters of heterophase equilibrium of ion exchange. In the experiment conditions, the quantity of the released cations was nearly 10 times larger than the quantity of the sorbed cations. The equilibrium parameters, determined from the model of pseudo second order reaction, were compared with the parameters obtained after 30 min of the process duration, ie at relatively stable indications of measuring equipment. On the example of the sorbed copper, the difference is approximately 8%. It was confirmed that the solution conductivity is a good parameter for the estimation of the state close to equilibrium.

2018 ◽  
Vol 18 (4) ◽  
pp. 733 ◽  
Author(s):  
Alexandr Ivanovich Vezentsev ◽  
Dang Minh Thuy ◽  
Lidia Fedotovna Goldovskaya-Peristaya ◽  
Nadezhda Alexandrovna Glukhareva

The adsorption of methylene blue from model aqueous solutions on bentonite-like clay, hydroxyapatite, and a composite sorbent has been investigated. The kinetic and thermodynamic parameters of adsorption in the temperature range 298–333 К have been calculated. The process is found to obey Langmuir isotherm equation. It is spontaneous but slightly endothermic. The maximal sorption capacity of the composite sorbent toward methylene blue is 175.4 mg/g at 25 °С that is 1.3 times more than that for bentonite-like clay and 17.8 times more than that for hydroxyapatite. Kinetics of the process is due to the combination of external and internal diffusion and can be described better by the model of pseudo-second order reaction.


1983 ◽  
Vol 48 (11) ◽  
pp. 3279-3286
Author(s):  
Slavko Hudeček ◽  
Miloslav Bohdanecký ◽  
Ivana Hudečková ◽  
Pavel Špaček ◽  
Pavel Čefelín

The reaction between hexamethylenediisocyanate and 1-pentanol in toluene was studied by means of reversed-phase liquid chromatography. By employing this method, it was possible to determine all components of the reaction mixture including both products, i.e. N-(6-isocyanate hexyl)pentylcarbamate and N,N'-bis(pentyloxycarbonyl)hexamethylenediamine. Relations for the calculation of kinetic constants were derived assuming a competitive consecutive second-order reaction. It was demonstrated that the reaction involved in this case is indeed a second-order reaction, and the rate constants of the first and second consecutive reactions were determined.


2017 ◽  
Vol 18 (1) ◽  
pp. 14-22 ◽  
Author(s):  
Selim Selimoglu ◽  
Esra Bilgin Simsek ◽  
Ulker Beker

Abstract In the current work, alumina modified natural zeolite (Z-Al) was used for fluoride adsorption in aqueous solution. Effects of process parameters such as pH, temperature, initial concentration and contact time were investigated. Box–Behnken design was found effective in defining the operating conditions for fluoride sorption onto Z-Al. Confirmatory experiments were conducted to examine the reliability of the regression equation. The predicted (2.261 mg g−1) and experimental (2.289 mg g−1) capacities were found to be similar, demonstrating the accuracy of the model. The fluoride adsorption onto Z-Al was well described by the Freundlich model. Kinetic studies revealed that the adsorption followed a pseudo-second-order reaction. Thermodynamic parameters depicted that the fluoride adsorption on the alumina modified zeolite was a spontaneous and exothermic process. The co-existing ions affected the defluoridation performance significantly. Regeneration of exhausted Z-Al was achieved with H2SO4.


Author(s):  
lon Ganescu ◽  
George Bratulescu ◽  
Ion Papa ◽  
Anca Ganescu ◽  
Alin Barbu ◽  
...  

Salvation kinetics of [Cr(NCS)4(imidazole)2]- has been studied in ethanol-water mixtures at different temperatures. The first stage of the solvation consists of two competitive reactions: two NCS- ions are exchanged, presumably, by water molecules and simultaneously an imidazole molecule by ethanol, the latter in a second-order reaction, accelerated by hydrogen ions. The exchange of the amine is followed by the substitution of the first two NCS- ions. The third and fourth NCS- ions are substituted only in neutral and slightly acidic solutions. Kinetic parameters have been determined for reactions (1), (2), and (4). The influence of the solvent composition and acidity is discussed


2000 ◽  
Vol 65 (12) ◽  
pp. 857-866
Author(s):  
Mladjen Micevic ◽  
Slobodan Petrovic

The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate (soman) was examined with a series of alkoxides and in corresponding alcohols: methanol, ethanol, 1-propanol, 2-propanol, 2-methoxyethanol and 2-ethoxyethanol. Soman reacts with the used alkoxides in a second order reaction, first order in each reactant. The kinetics of the reaction between 1,2,2-trimethylpropyl-methylfluorophosphonate and ethanol in the presence of diethylenetriamine was also examined. A third order reaction rate constant was calculated, first order in each reactant. The activation energy, frequency factor and activation entropy were determined on the basis of the kinetic data.


1930 ◽  
Vol 3 (4) ◽  
pp. 650-659
Author(s):  
John T. Blake

Abstract A procedure for the determination of combined selenium in rubber has been evolved. The rate of combination of selenium and rubber has been ascertained under certain conditions and shown to follow a first-order equation. A minimum value for the molecular weight of rubber has been estimated. The formation of hard rubber under chosen experimental conditions has been put on a mathematical basis and has been shown to follow a second-order reaction. The soft- and hard-rubber reactions have been shown qualitatively to be successive reactions and the function of accelerators has been discussed. The theory explains the anomalous results obtained by previous investigators.


2014 ◽  
Vol 7 ◽  
pp. ASWR.S16488 ◽  
Author(s):  
Ruchi Pandey ◽  
Nasreen Ghazi Ansari ◽  
Ram Lakhan Prasad ◽  
Ramesh Chandra Murthy

This paper describes the adsorption of Cd(II) ions from aqueous solutions by modified Cucumis sativus peel (CSP) by HCl treatment. The optimum pH, adsorbent mass, contact time, and initial ion concentration were determined. The maximum removal efficiency was 84.85% for 20 mg/L Cd(II) ion at pH 5. The adsorption isotherms were obtained using concentrations of the metal ions ranging from 5 to 150 mg/L. The adsorption process follows Langmuir isotherm and pseudo-second-order reaction kinetics. CSPs exhibit monolayer adsorption capacity of 58.14 mg/g at 298 K. The paper also discusses the thermodynamic parameters of the adsorption (the Gibbs free energy, entropy, and enthalpy). Our results establish that the adsorption process was spontaneous and endothermic under normal conditions.


2019 ◽  
Vol 19 (2) ◽  
pp. 55-63
Author(s):  
S. A. Ndur ◽  
H. Osei ◽  
C. E. Abbey ◽  
T. Joe-Asare

AbstractArsenic (As) has the potential to negatively affect soils and groundwater quality, and cause several public health challenges. It is usually concentrated and released during metal mining of ores that contains arsenic-bearing minerals. Remediation strategies are in place to avoid pollution. In this study, bauxite from Awaso, Ghana, was characterised, and its ability to sequester As was tested under varying conditions of temperature, Eh and pH. The study showed that the best particle size in the range utilised was 80% passing 2 mm as it allowed easy percolation, and As removal was about 95%. The reaction is a favourable pseudo-second order reaction that is spontaneous and thermodynamically stable and compares well with the Langmuir Sorption Isotherm. About 80% sorption was achieved within 20 minutes of contact with low desorption rate of less than 1.8%. The study thus concludes that bauxite is a good filter for arsenic. Keywords: Arsenic, Bauxite, Filter, Sorption, Isotherm


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