Isothermal, Kinetic, and Thermodynamic Studies on the Adsorption of Molybdenum by a Nanostructured Magnetic Material

In this study, the magnetic 3-(trimethoxysilyl) propyl methacrylate (TMSPMA) – poly (4-vinylpyridine) (P4VP) was synthesized and characterized. Removal of Molybdenum (Mo) from aqueous solutions using prepared material as nanosorbent was investigated. The magnetic P4VP was prepared by copolymerization of P4VP with TMSPMA. The prepared adsorbent was characterized by various techniques including the X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR). The batch adsorption technique was applied and the effect of several important parameters such as pH of the aqueous solution, adsorbent dose, initial Mo(VI) concentration, contact time, and temperature was evaluated. Desorption behavior of Mo(VI) and the effect of foreign ions (Cd2+, Ca2+, Co2+, Fe3+, Ba2+ and Pt4+) in real samples were also investigated. Co (II) and Pt (IV) had a greater impact on the adsorption process than other foreign ions. The maximum capacity for Mo(VI) adsorption on the prepared adsorbent was 4.87 mg/g, which was obtained at a temperature of 40°C with an initial concentration of 10 mg/L of Mo(VI). The adsorption isotherms were best fitted with the Weber Van Vliet isotherm model. The kinetic data were fitted well with the pseudo-second-order equation with a high correlation coefficient (R2 > 0.99). Based on the negative standard Gibbs free energy change (ΔG° < 0) and the positive standard enthalpy change (ΔH° > 0), it was found that the adsorption was an endothermic and a spontaneous process in nature.

Structure and Stability of Gas Adsorption Complexes in Periodic Porous Solids as Studied by VTIR Spectroscopy: An Overview

Variable-temperature infrared (VTIR) spectroscopy is an instrumental technique that enables structural characterization of gas-solid adsorption complexes by analysis of meaningful vibrational modes, and simultaneous determination of the standard enthalpy change (ΔH0) involved in the gas adsorption process, which allows one to quantify the stability of the corresponding complex. This is achieved by a van’t Hoff analysis of a set of IR spectra recorded over a sufficiently large temperature range. Herein, the use of this versatile spectroscopic technique is demonstrated by reviewing its application to the study of carbon monoxide, carbon dioxide and dinitrogen adsorption on several (alkaline) zeolites, which can be regarded as the archetype of periodic porous solids.

Adsorption behavior of Fe (III) in aqueous solution on melamine

This paper focused on the adsorption behavior of Fe (III) in aqueous solution on melamine. The effects of experimental conditions including dosage of melamine, reaction time and reaction temperature were investigated. The results showed that nearly 99% Fe (III) was adsorbed under the optimal conditions: melamine dosage (mole ratio) at n(C3H6N6)/n(Fe) = 3.5:1, reaction time of 60 min and reaction temperature of 90 °C. The optimal processing factors were obtained from response surface methodology and the effects of processing parameters on the removal efficiency of Fe (III) followed the order: mole ratio (n(C3N6H6):n(Fe)) &gt; reaction temperature &gt; reaction time. The adsorption kinetics behavior was fitted well with the pseudo-second-order model. The thermodynamic study showed that the adsorption process was unspontaneous and endothermic. The value of free energy change and standard enthalpy change disclosed that the mechanism of adsorption onto melamine was physisorption. The results will be useful for further applications of system design in the treatment of practical waste effluents.

Chemical Exergy of Fuels and Efficiency Analysis of Energy Utilizations

Many studies have investigated the chemical exergy of fuels. The results showed that it is equal to the negative standard free enthalpy change (SFEC) of the fuel combustion or the correction value. However, because the products of the combustion still have the chemical potentials of diffusion, the negative SFEC is not the whole of the chemical exergy of fuels. Because the accurate entropy of fuels cannot be obtained, the accuracy of the SFEC is doubtful and some corrections become necessary. But any correction risks misrepresenting the exergy balance of fuel-fired energy systems. In this paper, some important thermodynamic fundamental problems were studied, which showed that the chemical exergy of fuels should be equal to the negative standard enthalpy change. The formulas of total entropy generations and exergy efficiencies of energy utilizations were deduced, so that the exergy efficiency evaluation just needs heat balance data. The case studies were also given.

Studies on the adsorption of amoxicillin on multi-wall carbon nanotubes

This study examined the feasibility of removing amoxicillin (AMO) from aqueous solutions using multi-wall carbon nanotubes. The equilibrium adsorption data were analyzed using four widely applied isotherms: Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich. The results showed that the Langmuir isotherm model fits well the obtained experimental data. The adsorption process followed the pseudo-second-order model. The activation energy was found to be 19 kJ/mol. The Standard free energy changes, ΔG0, values were negative; the standard enthalpy change (ΔH0), and standard entropy change (ΔS0) values of the process were 4 kJ/mol and 36 J/mol.K. Results suggested that the AMO adsorption on carbon nanotubes was a spontaneous process.

Spectroscopic investigation of the interaction of bovine serum albumin with a novel cardiac agent V-09

This study employs fluorescence spectroscopy to characterize the binding properties of a newly synthesized cardiac agent, V-09, on bovine serum albumin (BSA). This compound shows the highest cardiac activity in the whole series. The binding constantsKat 25°C and 37°C are obtained, the values are 7.12×104l mol–1, 4.66×104l mol–1, respectively. The standard enthalpy change (ΔH0) and the standard entropy change (ΔS0) are calculated to be –27.13 KJ mol–1and 1.854 J mol–1K–1, which indicated that hydrophobic forces play major role in the interaction between V-09 and BSA. The binding average distance between V-09 and BSA (2.57 nm) is obtained on the basis of the theory of Főrster energy transfer.

Thermodynamic characterization of the dimerization equilibrium of newly synthesized polymethine cyanine dyes

The monomer-dimer equilibrium and thermodynamics of three new cyanine dyes were investigated by spectrophotometric and chemometric methods. The dimerization constants of these new cyanine dyes were determined by studying the dependence of their absorption spectra on the temperature in the range 25-80?C at concentrations of 3.0?10-4, 1.9?10-4 and 1.1?10-4 M for dye 1, 2 and 3, respectively. The processing of the data, performed for the quantitative analysis of pure spectral profiles, was based on the simultaneous resolution of the overlapping bands in the whole set of absorption spectra. From the dimerization constant and its dependence on temperature, the values of the standard enthalpy change and entropy change of dimerization were calculated.

Adsorption of Liquids and Swelling of Wood IV. Temperature Dependence on the Adsorption

Summary For the purpose of understanding the swelling phenomenon of wood in liquids, the contributions of enthalpic and entropic terms to the standard free energy change of adsorption have been determined by measuring the temperature dependence of adsorption isotherms. The values of standard enthalpy change of adsorption are smaller for alcohols having both proton-accepting and -donating properties than for acetone having only a proton-accepting property. The results are discussed in terms of the proton-accepting power and the cohesive energy of the respective adsorbate liquids. Methanol showed a larger isosteric heat of adsorption to dried wood than to pre-swollen wood, and the amounts of methanol and acetone adsorbed on dried wood exceeded those on swollen wood within the low activity range. These results indicate the presence of more exothermic sites in dried wood than in pre-swollen wood, and of pre-existing spaces and/or parts loosely hydrogen-bonded between wood constituents in the cell walls of dried wood.

The Equilibrium and the Determination of D00 (H—CN)

The rate constants and equilibrium constant for the proton transfer reaction [Formula: see text] have been measured at 296 ± 2 K using the flowing afterglow technique: kforward = (2.9 ± 0.6) × 10−9 cm3molecule−1s−1, kreverse = (1.8 ± 0.4) × 10−10 cm3 molecule1 s−1, and K = 16 ± 2. The measured value of K corresponds to a standard free energy change, ΔG296°, of −1.6 ± 0.1 kcal mol−1 which provides values for the standard enthalpy change, ΔH298°= −1.0 ± 0.2 kcal mol−1, the bond dissociation energy, D00(H—CN) = 124 ± 2 kcal mol−1, and the proton affinity, p.a.(CN−) = 350 ± 1 kcal mol−1.

A method for investigating the effect of temperature on the 695 nm band of insoluble cytochrome c

A method is described for computer analysis of simple spectrophotometric changes in particulate systems, and this has been applied to the bleaching of the 695 nm band of insoluble ferricytochrome c by temperature. The results show that insolubilization has no effect on the standard enthalpy change but lowers the value for the standard entropy change. This effect appears to be independent of the concentration of the gel matrix to which the cytochrome c is bound, but dependent on the ionic strength of the surrounding solution.