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Number of results: 37
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Abstract

This study investigates the influence of four imidazolium ionic liquids (ILs) present in wastewater on the activated sludge process. In addition, experiments with inactivated sludge to assess the capacity of this sorbent to remove ILs from the wastewater were conducted. It occurred that the presence of ionic liquids in wastewater reduces biomass growth and size of the sludge flocs. The strongest effect has been found for IL 6 (1-hexyl-2H-3-methyl-4,5-dimethylimidazolium iodide) with the longest alkyl chain length. Also, the degree of ILs removal increases with the alkyl chain length and decreases with the increase of initial concentration of ILs in wastewater. IL 6 reaches the highest degree of ILs removal from wastewater but inhibits the biomass growth and growth of sludge flocs in a greater extent than other tested compounds. Moreover, it was confirmed that newly synthesized ionic liquids can be adsorbed onto inactivated sludge. IL 6 could be adsorbed in a higher degree than other ionic liquids. This adsorption was described by Langmuir isotherm, whereas adsorption of other ionic liquids was described by Freundlich isotherm.
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Abstract

This study investigates the estimated adsorption efficiency of artificial Nickel (II) ions with perlite in an aqueous solution using artificial neural networks, based on 140 experimental data sets. Prediction using artificial neural networks is performed by enhancing the adsorption efficiency with the use of Nickel (II) ions, with the initial concentrations ranging from 0.1 mg/L to 10 mg/L, the adsorbent dosage ranging from 0.1 mg to 2 mg, and the varying time of effect ranging from 5 to 30 mins. This study presents an artificial neural network that predicts the adsorption efficiency of Nickel (II) ions with perlite. The best algorithm is determined as a quasi-Newton back-propagation algorithm. The performance of the artificial neural network is determined by coefficient determination (R2), and its architecture is 3-12-1. The prediction shows that there is an outstanding relationship between the experimental data and the predicted values.
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Abstract

In this review, research carried out on sorption-enhanced steam methane reforming (SESMR) process is presented and discussed. The reactor types employed to carry out this process, fixed packed bed and fluidized bed reactors, are characterized as well as their main operating conditions indicated. Also the concepts developed and investigations performed by the main research groups involved in the subject are summarized. Next the catalysts and CO2 sorbents developed to carry out SE-SMR are characterized and the relationships describing the reaction and sorption kinetics are collected. A general approach to model the process is presented as well as results obtained for a calculation example, which demonstrate the main properties of SE-SMR.
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Abstract

A review is given on a number of colloidal phenomena with special reference to their applicability to nanoparticles. Phenomena addressed include preparation, electric double layers and their characterization, electrokinetics, van der Waals and Lifshits forces, electric and steric particle interaction.
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Abstract

HY2SEPS was an EU-funded project directed at the reduction of CO2 emissions. The principal objective of the project was to develop a hybrid membrane-adsorptive H2/CO2 separation technique that would form an integral element of the pre-combustion process. Specific tasks included the derivation of simplified mathematical models for the membrane separation of H2/CO2 mixtures. In the present study one of the developed models is discussed in detail, namely that with the countercurrent plug flow of the feed and the permeate. A number of simulations were carried out concerning the separation of binary mixtures that may appear following steam conversion of methane. The numerical results were then compared with the experimental data obtained by FORTH/ICEHT. The estimated fluxes of pure CO2, H2, CH4 and N2 are shown alongside those measured experimentally as a function of temperature and CO2 partial pressure in Figs 2 - 7. It is concluded that, in general, CO2 flux increases monotonically with both temperature and CO2 partial pressure. It is also found that the fluxes of hydrogen, methane and nitrogen reach a minimum at a temperature slightly above 323 K. Overall, a good agreement was obtained between the simulations and experiments.
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Abstract

Adsorption experiments of nitric oxide in nitrogen carrier gas were held on activated carbon in a fixed bed flow system. Breakthrough curves describing the dependence of exit concentrations of nitric oxide on time were matched with theoretical response curves calculated from the linear driving force model (LDF). The model assumes Langmuir adsorption isotherm for the description of non-linear equilibrium and overall mass transfer coefficient for mass transfer mechanism. Overall mass transfer coefficients were obtained by the method of least squares for fitting numerically modelled breakthrough curves with experimental breakthrough curves. It was found that LDF model fits all the breakthrough curves and it is a useful tool for modelling purposes.
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Abstract

Point of present exploration was to figure out the anticorrosion activity of Acacia Cyanophylla (Saligna leaves) extract on the corrosion of mild steel in dilute sulfuric acid medium, using weight loss measurements and electrochemical impedance spectroscopy. The result of the study revealed that the extract act as a potent inhibitor on mild steel in acid medium. The increase in inhibitor concentration and immersion time showed a positive effect on inhibition efficiency. EIS exhibited one capacitive loop which indicates that the corrosion reaction is controlled by charge transfer process. The increase of phase shift (n) in presence of (ACLE) lower surface roughness. This change reveals the adsorption of the inhibitor compound on the steel surface. According to the results of weight loss measurements, the adsorption of the extract on the steel surface can be described by the Langmuir isotherm. The inhibition mechanism of (ACLE) molecules involves physical interaction between the inhibitor and metal surface. Additionally, Protective film formation against acid attack was confirmed by FT-IR and AFM techniques.
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Abstract

A laboratory study was performed to study the effects of various operating factors, viz. adsorbent dose, contact time, solution pH, stirring speed, initial concentration and temperature on the adsorption of triphenyltin chloride (TPT) onto coal fly ash supported nZnO (CFAZ). The adsorption capacity increases with increase in the adsorbent amount, contact time, pH, stirring speed and initial TPT concentration, and decrease with increase in the solution temperature. The adsorption data have been analyzed by Langmuir, Freundlich, Temkin and Dubinin-Radushkevich (D-R) adsorption models to determine the mechanistic parameters associated with the adsorption process while the kinetic data were analyzed by pseudo first-order, pseudo second-order, Elovich, fractional power and intraparticle diffusivity kinetic models. The thermodynamic parameters of the process were also determined. The results of this study show that 0.5 g of CFAZ was able to remove up to 99.60% of TPT from contaminated natural seawater at 60 min contact time, stirring speed of 200 rpm and at a pH of 8. It was also found that the equilibrium and kinetic data fitted better to Freundlich and pseudo second-order models, respectively. It can therefore be concluded that CFAZ can be effectively used for shipyard process wastewater treatment
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Abstract

In the present study, the novel quaternary ammonium salt (QAS+), 1-methyl-di-octyl-1 phenyl ammonium iodide (QAS1), was synthesized by complete alkylation reaction. Sodium montmorillonite (Mt) was modified via an ion-exchange reaction with QAS1+. The modified material and quarternary ammonium salt (Mt1 and QAS1) were analyzed by nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). Removal capacity of hydrophobic organic pollutants such as 4-nitrophenol (4-NP) and 2,4-dinitrophenol (2,4-DNP) from solution media of synthesized organoclay was evaluated. The optimum conditions and batch kinetics of adsorption of 4-nitrophenol and 2,4-dinitrophenol from aqueous solutions are reported. It was shown that the adsorption capacity decreased in the order 4-NP> 2,4-DNP. The total mass loss during the drying process was 66% and 78%, respectively. Thermodynamic parameters enthalpy (∆H0) and entropy (∆S0) and the mean free energy (E) for the adsorption of nitrophenol compounds (NCP) were determined.
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Abstract

The adsorption of lead ions onto a zeolite bearing tuff (stilbite) from synthetic acid aqueous solution and acid mine drainage taken from Sasa mine, Macedonia, is elaborated in this paper. The results present that adsorption occurs effi ciently in both of cases. The physical and chemical properties of the used natural material, zeolite bearing tuff, are characterized by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy. The concentration of metal ions in solution before and after treatment is obtained by AES-ICP. The effectivity of zeolite bearing tuff is determined through a series of experiments under batch conditions from single ion solutions, whereby the main parameters are the effects of initial pH of solution, mass of adsorbent, initial metal concentration in solution, contacting time and competing cations. The maximum capacity of zeolite bearing tuff for removal of lead ions from solution is determined by equilibrium studies. The experimental obtained data are fi tted with Freundlich and Langmuir adsorption models. The experimental data are better fi tted with Langmuir adsorption isotherm. Zeolite bearing tuff is effective adsorbent for treating acid mine drainage. The results showed that 99% of lead ions are removed from acid mine drainage, i.e. the concentration of lead ions from 0.329 mg/dm3 decrease to 0.002 mg/dm3 . The pH value of acid mine drainage from 3.90 after treatment with zeolite bearing tuff increases to 5.36.
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Abstract

The objective of this study was to investigate the possibility of using natural and bacteria-modified Erzurum clayey soil with Methylobacterium extorquens as an alternative to high cost commercial adsorbent materials for the removal of copper from aqueous solution. The copper concentrations in the samples of the polluted river water and CuCl2 solutions treated by the natural and bacteria-modified Erzurum clayey soil (ECS) have been determined by spectrophotometric method. Firstly, the surface of ECS was modified with M. extorquens and surface functionality was increased. Then, the adsorption of Cu (II) from solution phases was studied with respect to varying metal concentration, pH, and temperature and agitation time. The maximum adsorption of Cu (II) for natural and bacteria-modified Erzurum clayey soil was observed at pH: 5.0. At different copper concentrations, copper adsorption analysis was performed on 1 g using clay soil or modified clay soil. Maximum adsorption of Cu (II) was obtained as 45.7 and 48.1 mg g-1 at initial concentration (50 mg/50 mL) and optimal conditions by natural and bacteria-modified clay soil, respectively. The copper concentration was decreased in the substantial amount of the leachates solutions of natural and bacteria-modified clay soil. Langmuir and Freundlich isotherms were used to describe the adsorption behavior of Cu (II) ions. The results showed that modified clay soil had a high level of adsorption capacity for copper ion. The various thermodynamic parameters such as ΔG°, ΔH° and ΔS° were analyzed to observe the nature of adsorption. The structural properties of the natural and bacteria-modified-ECS have been characterized by SEM, FTIR and XRD techniques. Consequently, it was concluded that the bacteria-modified clay soil could be successfully used for the removal of the copper ions from the aqueous solutions.
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Abstract

This paper presents a general overview of 2D mathematical models for both the inorganic and the organic contaminants moving in an aquifer, taking into consideration the most important processes that occur in the ground. These processes affect, to a different extent, the concentration reduction values for the contaminants moving in a groundwater. In this analysis, the following processes have been taken into consideration: reversible physical non-linear adsorption, chemical and biological reactions (as biodegradation/biological denitrification) and radioactive decay (for moving radionuclides). Based on these 2D contaminant transport models it has been possible to calculate numerically the dimensionless concentration values with and without all the chosen processes in relation to both the chosen natural site (piezometers) and the chosen contaminants.In this paper, it has also been possible to compare all the numerically calculated concentration values to the measured concentration ones (in the chosen earlier piezometers) in relation to both the new unpublished measurement series of May 1982 and the new set of parameters used in these 2D contaminant transport models (as practical verification of these models).
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