Biosorption Of Copper Ions Research Articles

Biosorption of Cu(II) from aqueous solution by Fucus serratus: Surface characterization and sorption mechanisms

In this work, the brown alga Fucus serratus ( FS) used as a low cost sorbent has been studied for the biosorption of copper(II) ions in batch reactors. Firstly, the characterization of the surface functional groups was performed with two methods: a qualitatively analysis with the study of FT-IR spectrum and a quantitatively determination with potentiometric titrations. From this latter, a total proton exchange capacity of 3.15 mmol g −1 was extrapolated from the FS previously protonated. This value was similar to the total acidity of 3.56 mmol g −1 deduced from the Gran method. Using the single extrapolation method, three kinds of acidic functional groups with three intrinsic p K a were determined at 3.5, 8.2 and 9.6. The point of zero net proton charge (PZNPC) was found close to pH 6.3. Secondly, the biosorption of copper ions was studied. The equilibrium time was about 350 min and the adsorption equilibrium data were well described by the Langmuir’s equation. The maximum adsorption capacity has been extrapolated to 1.60 mmol g −1. The release of calcium and magnesium ions was also measured in relation to the copper biosorption. Finally, the efficiency of this biosorbent in natural tap water for the removal of copper was also investigated. All these observations indicate that the copper biosorption on FS is mainly based on ion exchange mechanism and this biomass could be then a suitable sorbent for the removal of heavy metals from wastewaters.

Biosorption of copper ions from dilute aqueous solutions on base treatedrubber (Hevea brasiliensis) leaves powder: kinetics, isotherm, and biosorption mechanisms

The efficiency of sodium hydroxide treated rubber (Hevea brasiliensis) leaves powder (NHBL) for removing copper ions from aqueous solutions has been investigated. The effects of physicochemical parameters on biosorption capacities such as stirring speed, pH, biosorbent dose, initial concentrations of copper, and ionic strength were studied. The biosorption capacities of NHBL increased with increase in pH, stirring speed and copper concentration but decreased with increase in biosorbent dose and ionic strength. The isotherm study indicated that NHBL fitted well with Langmuir model compared to Freundlich and Dubinin-Radushkevich models. The maximum biosorption capacity determined from Langmuir isotherm was 14.97 mg/g at 27 degrees C. The kinetic study revealed that pseudosecond order model fitted well the kinetic data, while Boyd kinetic model indicated that film diffusion was the main rate determining step in biosorption process. Based on surface area analysis, NHBL has low surface area and categorized as macroporous. Fourier transform infrared (FT-IR) analyses revealed that hydroxyl, carboxyl, and amino are the main functional groups involved in the binding of copper ions. Complexation was one of the main mechanisms for the removal of copper ions as indicated by FT-IR spectra. Ion exchange was another possible mechanism since the ratio of adsorbed cations (Cu2+ and H+) to the released cations (Na+, Ca2+, and Mg2+) from NHBL was almost unity. Copper ions bound on NHBL were able to be desorbed at > 99% using 0.05 mol/L HCl, 0.01 mol/L HNO3, and 0.01 mol/L EDTA solutions.

Copper removal by algae Gelidium, agar extraction algal waste and granulated algal waste: Kinetics and equilibrium

Biosorption of copper ions by an industrial algal waste, from agar extraction industry has been studied in a batch system. This biosorbent was compared with the algae Gelidium itself, which is the raw material for agar extraction, and the industrial waste immobilized with polyacrylonitrile (composite material). The effects of contact time, pH, ionic strength (IS) and temperature on the biosorption process have been studied. Equilibrium data follow both Langmuir and Langmuir–Freundlich models. The parameters of Langmuir equilibrium model were: q max = 33.0 mg g −1, K L = 0.015 mg l −1; q max = 16.7 mg g −1, K L = 0.028 mg l −1 and q max = 10.3 mg g −1, K L = 0.160 mg l −1 respectively for Gelidium, algal waste and composite material at pH = 5.3, T = 20 °C and IS = 0.001 M. Increasing the pH, the number of deprotonated active sites increases and so the uptake capacity of copper ions. In the case of high ionic strengths, the contribution of the electrostatic component to the overall binding decreases, and so the uptake capacity. The temperature has little influence on the uptake capacity principally for low equilibrium copper concentrations. Changes in standard enthalpy, Gibbs energy and entropy during biosorption were determined. Kinetic data at different solution pH (3, 4 and 5.3) were fitted to pseudo-first-order and pseudo-second-order models. The adsorptive behaviour of biosorbent particles was modelled using a batch reactor mass transfer kinetic model, which successfully predicts Cu(II) concentration profiles.

Intensification of biosorption of copper ions from solution by the yeast Saccharomyces cerevisiae in magnetic field

We studied the possibility of intensification of biosorption of copper ions by the yeast Saccharomyces cerevisiae 1968 from a copper sulfate solution by immersing a metal 80-rod headpiece into the solution and applying an external magnetic field. The field was parallel or perpendicular to the axes of headpiece rods. It was shown that intensification of extraction of copper ions at various geometries of the system differed insignificantly and that copper ions were extracted from the solution via biosoprtion and cementation at the metal headpiece.

EPR examination of Zn 2+ and Cu 2+ binding by pigmented soil fungi Cladosporium cladosporioides

The purpose of this study was to examine the usefulness of electron paramagnetic resonance spectroscopy (EPR) to estimate zinc and copper ions biosorption from the environment by pigmented soil fungi Cladosporium cladosporioides. The existence of a low amount of pheomelanin, besides eumelanin, in C. cladosporioides samples was proved by the analysis of shape of their EPR spectra. Concentration of o-semiquinone free radicals in crude mycelium was 2.4 × 10 17 spin/g. Changes in free radicals system of C. cladosporioides cultured in the presence of Zn 2+ and Cu 2+ were analysed. Both magnetic and chemical interactions of zinc and copper ions with free radicals in C. cladosporioides melanin were found. Magnetically interacting diamagnetic Zn 2+ ions increased the concentration of o-semiquinone free radicals in melanin existing in C. cladosporioides mycelium, whereas paramagnetic Cu 2+ ions decreased this concentration. Chemical interactions of Zn 2+ and Cu 2+ ions decreased the free radical concentrations in C. cladosporioides melanin. Homogeneously distributed free radicals in C. cladosporioides melanin rise its activity in biosorption processes.

Study of Cu(II) biosorption by dried activated sludge: effect of physico-chemical environment and kinetics study

Biosorption is a recent technology used to remove heavy metal ions from aqueous solutions. The biosorption of copper ions from aqueous solution by dried activated sludge was investigated in batch systems. Effect of solution pH, initial metal concentration and particle size range were determined. The suitable pH and temperature for studied conditions were determined as 4.0 and 20 °C, respectively. The theoretical max biosorption capacity of activated sludge was 294 mg g −1 at 20 °C for <0.063 mm particle size. The equilibrium data fitted very well to both Langmuir and Freundlich isotherm models. The pseudo first and second-order kinetic models were used to describe the kinetic data. The experimental data fitted to second-order kinetic model. The particle size and initial metal concentration were effected the biosorption capacity of dried activated sludge. An increase in the initial metal concentration increases of biosorption capacity, which also increases with decreasing particle size. Dried activated sludge has different functional groups according to the FT-IR results.

Biosorption of copper ions by dried leaves: chemical bonds and site symmetry

The biosorption of copper by dried leaves was studied by Fourier transform infrared spectroscopy (FTIR) and electron paramagnetic resonance (EPR). From FTIR measurements, we conclude that the presence of copper ions in the biomass affects the bands corresponding to CC vibrations of carbon rings of the biomass. In the EPR spectra, the Cu 2+ ion is seen to be incorporated into the biomass in a site with an axial symmetry. We propose a model for the sorption site where the copper ions are located between two adjacent carbon rings in an interstitial site in the fibers of the biomass.

Biosorption of copper by dried plant leaves studied by electron paramagnetic resonance and infrared spectroscopy

We report on the biosorption of copper ions by dried leaves from the Brazilian flora. By Electron Paramagnetic Resonance (EPR), it is shown that the copper ions are incorporated in the leaves in a strongly axial site. Washing with a basic solution does not remove the copper from the leaves, however, it modifies the axial site symmetry. Infrared absorption seems to be compatible with a site that is located near to a simple or a double carbon–oxygen bond. Dried leaves are a good and commercially interesting alternative for sorption of metal ions compared to other biomasses.