Kinetic Isotherm of Amoxicillin Antibiotic through Adsorption and its Removal by Electrocoagulation

Antibiotics are emerging contaminants in the aquatic environment because they have adverse effects on the aquatic life and humans. The use of antibiotics in human and veterinary medicine has a significant effect on the quality of surface and groundwater. The relevance of an electrocoagulation (EC) process for the removal of an antibiotic was selected because of its wide application, high solubility in water, high residual toxicity and an absence of biodegradability, was examined in this study. Metal hydroxides generated during EC were used to remove Amoxicillin (AMX) from aqueous solution. The knowledge regarding the removal mechanism of this substance has not yet been investigated till now. Experiments were carried out in a batch electrochemical reactor using aluminum electrodes. The removal of AMX was relatively fast and equilibrium was reached within 20 min. The effects of the main operating parameters were examined and showed that irrespective of the initial concentration and for pH ranging from 3 to 10, maximum removal efficiency remained close to 95%; while a sharp decrease was recorded at pH 2 (8 % removal). The results of this study also showed that the removal of AMX from water was strongly affected by the current intensity. The mechanism of electrocoagulation was modeled using isotherm models and showed that the Sips isotherm matched satisfactorily the experimental data, suggesting monolayer coverage of adsorbed molecules and assumed a quasi-Gaussian distribution energy owing to the high correlation also found for the Toth model. In addition, adsorption kinetic studies showed that the EC process followed a pseudo-second-order kinetic model at the various current densities, as when the pH and initial antibiotic concentrations were considered.


INTRODUCTION
Amoxicillin is a moderate-spectrum (3lactam antibiotic used to treat bacterial infections caused by susceptible microorganisms.From an to determine the concentrations of antibiotics in the environment, and from this information the health effects to humans and animals may be estimated by toxicologists.Traditionally, the impact of chemical pollution has focused almost exclusively on the conventional priority pollutants.However, the growing use of pharmaceuticals worldwide, classified as the so-called emerging pollutants, has become a new environmental problem, which has raised great concern among scientists in the last few years.More than 3,000 chemical products are used in human and veterinary medicine .The use of antibiotics in human and veterinary has a significant effect on the quality of surface and ground water.Among veterinary pharmaceuticals, antibiotics are widely prescribed.At present, it has been reported that AMXs have been found in soils, surface water and groundwater.Frequent application of amoxicillin antibiotics has given cause for concern about increased antibiotic resistance of microorganisms in the terrestrial as well as aquatic environment and the effect of antibiotics on plant and aquatic growth.Amoxicillin is an antibiotic active against a wide range of Gram-positive, and a limited range of Gram-negative organisms.Amoxicillin acts by inhibiting the synthesis of bacterial cell walls.It inhibits cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell wall of Gram-positive bacteria.It is usually the drug of choice within the class because it is better absorbed, following oral administration, than other beta-lactam antibiotics.Amoxicillin is susceptible to degradation by (3lactamase-producing bacteria, and so may be given with clavulanic acid to decrease its susceptibilityThe presence of AMX and other antibiotics in natural environments can cause bacteria to acquire and transmit antibiotic-resistant genes, which potentially threatens ecosystem functions and human health.Even low concentrations of pharmaceuticals released from the environmental matrix into water can pose serious environmental damages.Thus, it is of great importance to develop some efficient and cost effective treatment technologies to remove such compounds.Various techniques such as ozonation , photo-Fenton process, photo-electro-catalytic degradation, ion exchange and other processes have been employed for the removal of antibiotics from water.Among these available methods, adsorption is a widely used effective technology for the treatment of low concentration antibiotics.Recently, adsorption of antibiotics on sorbents based on metal or metal oxides such as montmorillonite , hydrous oxides of aluminum and iron were reported.The present study proposes an electrocoagulation (EC) process for the removal of tetracycline, which was selected because of its wide application, high solubility in water, high residual toxicity and its absence of biodegradability.Recent research has demonstrated that electrocoagulation offers an attractive alternative method for treating water.EC treatment is characterized by simple and easy operated equipment, short operation time, no addition of chemicals and low sludge production.Iron or aluminum is generally employed as a sacrificial electrode material in EC process but other anodes like magnesium alloy and aluminium alloy can also be used.The dissolved metal ions, at an appropriate pH, can form a wide range of hydro complex species and metal hydroxides that destabilize and aggregate the suspended particles or precipitate and adsorb dissolved contaminants.The anodic and cathodic reactions for aluminium electrodes can be written as: At the anode Al (s) Al 3+ (aq) + 3e-...( 1) The generated Al(aq) 3+ ions combine with hydroxyl ions to form the metal hydroxides which are partly soluble in the water under definite pH values.Al 3+ and OH _ ions generated by electrode reactions (1) and (2) react to form various monomeric species such as Al(OH) 2+ , Al(OH) 2 + , Al2(OH)2 4+ , Al(OH)4 -, and polymeric species such as Al6(OH)15 3+ , Al7(OH)17 4+ , Al8(OH)20 4+ , Al13O4(OH)24 7+ , Al13(OH)34 5+ ,which transform finally into Al(OH)3(S) according to complex precipitation kinetics.
The polymeric aluminum complexes can have both positive and negative charges capable of attracting the opposite charge of polluting species and remove them from the solution.
Electrocoagulation is a complex and interdependent process strongly dependent on the chemistry of the aqueous medium.The electrolyte pH plays an important role in the separation of suspended particles; at low pH the separation is dominated by precipitation while adsorption dominates at high electrolyte pH.The Al(OH)3(s) formed "sweep flocs" have large surface areas which is beneficial for a rapid adsorption of soluble organic compounds and trapping of colloidal particles.Finally, these flocs can be easily removed from aqueous medium by sedimentation or H 2 flotation.In this study, a series of batch experiments were conducted.The removal efficiency was investigated by a series of experiments under different experimental conditions such as reaction time, solution pH, initial amoxicillin concentration and current intensity.To our knowledge, no report is available in the literature dealing with the reduction of AMX concentration in water using the EC process.

Theoretical part Electrocoagulation kinetics
The pollutant is generally adsorbed at the surface of the flocs electrochemically generated, following two consecutive separate processes: (i) An electrochemical process through which the metal flocs are generated; (ii) followed by a physicochemical process, namely adsorption on the surface of the flocs.The removal of pollutant is similar to conventional adsorption except the generation of coagulants.The electrode consumption can be estimated according to Faraday's Law and the amount of flocs generated can be stoichiometrically estimated.The formed aluminum floc traps the pollutant present in the solution by adsorption mechanism: From this, pollutant removal can be modeled by adsorption phenomena and the amount of adsorbed pollutant is: Where qa is the amount of amoxicillin (AMX) adsorbed per gram of medium (mg/g), V is the volume of solution (L), M is the weight of electrode dissolved (g); C0 and Ct are the initial concentration and the concentration of AMX at any time t (mg/L), respectively.In order to investigate the mechanisms of the adsorption process, various kinetic models: pseudo-first-order, pseudo-secondorder, Fractional Power and Elovich models were applied to describe the adsorption kinetics onto aluminum hydroxides.The most accurate model was selected according to the linear regression correlation coefficient values, R2.The pseudo-first order kinetic model can be given as: Where K1 (min-1) is the constant rate of adsorption, qt and qe are the adsorbed amounts at a given time t and at equilibrium (mg/g) respectively.After integration between 0 and a given time t, it comes: Which can be rearranged to give: The pseudo second-order model kinetic equation is : Where K2 is the rate constant of the pseudo-second order equation (g/mg/min).Integration leads to: The adsorption of AMX onto aluminum hydroxides was also examined by Elovich and Fractional Power.The linearized method was used to determine the parameters of the kinetic models.
The Elovich model kinetic equation is: The Elovich model was originally developed to describe the kinetics of heterogeneous chemisorptions of gases on solid surfaces.It has been used to describe the kinetics of sorption/desorption of various chemicals on solid phases.A plot of (qt) vs. (lnt) should give a linear relationship if the Elovich model is applicable, with a slope of 1/b and an intercept of 1/b ln(ab).
The Fractional Power or Power Function model kinetic equation is: qt = Ktn ... (11)   with  a positive constant (<1) and K a constant.The kinetic parameters were obtained from the plot ln(qt) vs ln(t), with a slope and an intercept of lnK.Equation 11 is empirical, except for the case where  = 0.5; then Eq.11 becomes similar to the Weber-Morris model.Equation 11and various modified forms have been used by a number of researchers to describe the kinetics of solid phase sorption/desorption and chemical transformation processes.

Adsorption isotherm
Since the removal of pollutant is similar to conventional adsorption, except the generation of coagulants, adsorption isotherm models can be extended to describe experimental isotherm data and identify the mechanism of the adsorption process.Isotherm models with two and three parameters have been therefore considered to establish the relationship between the amounts of amoxicillin adsorbed onto the aluminum hydroxides and its equilibrium concentration in the aqueous solution containing amoxicillin antibiotic.The general forms of both these models were described as follows.
The Langmuir equation: Where b (L/mg) is the binding constant and q0(mg/g) refers the maximum adsorption capacity, evaluated by potting the Ce/qe against Ce.
The Freundlich isotherm: Where Kf and n are the constants which give adsorption capacity and intensity respectively.

The Sips equation
In the Sips model (eq.14), qe and Ce are the adsorption capacity at equilibrium and the equilibrium concentration, q0 represents the maximum adsorption capacity, b the adsorption equilibrium constant and n the dissociation parameter.If n = 1, the Sips model reduces to the Langmuir model.qe = q 0 bCe n / 1+ bCe n ...( 14) The Toth equation The Toth model is derived from potential theory and is applicable to heterogeneous adsorption.This isotherm (Eq.( 15)) presupposes a quasi-Gaussian energy distribution.Most sites have an adsorption energy lower than the peak or maximum adsorption energy.qe = q0 Ce /(b + Ce m ) 1/m ...( 15)

Chemical and reagents
Amoxicillin hydrochloride (>95%) was obtained from Sigma-Aldrich (India).The molecular structure and pKa of AMX are shown in Fig. 1.AMX could have different charges on different sites depending on the pH.According to the speciation of AMX under various pHs, when solution pH is below 3.3, AMX exists as a cation, +00, due to the protonation of the organic group.At pH between 3.3 and 7.7, the zwitterion form, +-0, predominates due to the loss of a proton from the phenolic diketone moiety.At solution pH greater than 7.7, a monovalent anion +--, or a divalent anion 0--, from the loss of protons from the carbonyl system and phenolic moiety prevail.

Experiments
Experiments were carried out in a batch electrochemical reactor of 500 mL capacity (Fig. 2) with Aluminum / Aluminum as sacrificial anode of 28.5 cm2 of submerged area.The electrode distance between anode and cathode was maintained constant at a value of 2 cm during electrolysis.A direct current was supplied by a DC regulated power source.Proper agitation was provided to maintain an uniform concentration inside the cell.A stock solution was prepared by dissolving an appropriate quantity of amoxicillin in distilled water.The concentration of the supporting electrolyte was adjusted by adding KCl, and the amoxicillin solutions were characterized by measuring their conductivity, which was found to be 1.2 mS/cm.The pH of the solution was adjusted by adding diluted HCl or NaOH.The sample was collected at every 30 s interval and then analyzed by UV-Vis spectroscopy.Experiments have been duplicated and the error was found to be below 4%.

Amoxicillin measurement
Antibiotic concentrations were quantified by UV/Vis spectroscopy (UV-Vis -Systronics Spectrophotometer).Amoxicillin absorbance was measured at 360 nm.This wavelength is an isobestic point for this antibiotic.

Effect of the operating parameters Effect of the contact time
Fig. 3 shows the effect of the shaking time on the removal of AMX by electrocoagulation process.High removal rates of AMX were observed at the onset; and then plateau values were gradually reached within 15 min.The residual AMX concentration versus time showed a single, smooth and continuous curve until reaching saturation (Fig. 3), suggesting possible monolayer coverage of AMX on the surface of the sorbent produced in situ.

Effect of the current intensity
In all electrochemical process, the current density is the most important parameter for controlling the reaction rate within the electrochemical reactor.The current density is expected to exhibit a strong effect on EC, especially on the kinetics of removal, shortening the treatment.This is ascribed to the fact that at high current density, the extent of anodic dissolution of aluminum increases, resulting in a greater amount of precipitate for the removal of pollutants.Moreover, bubble generation rate increases with increasing current intensity.These effects are both beneficial for high pollutant removal by H2 flotation.To investigate the effect of the current density, a series of experiments were performed using 50 mg/L AMX containing solution, at pH=6, for current intensities varying from 0.1 to 0.8 A (Fig. 4).The removal efficiency of AMX increased rapidly up to 98% for a current intensity of 0.3 A after only 6 min (Fig. 4).It can also be observed that when the current intensity increased, the operating time decreased.For example, when the current intensity was increased from 0.1 to 0.8 A, the retention time of AMX solution in the electrocoagulation unit was shortened from 15 min to 5 min.This means that the electrocoagulation equipment can be almost three times smaller for 0.8 A current intensity.These results have to be related to the increase of the amount of Al3+ cations released by the anode and hence the increase of Al(OH)3 particles.However, the difference between the curves corresponding to different current intensity became small when it was higher than 0.3 A. An optimum current density can therefore be defined.For the experimental conditions of Fig. 4, optimal current seemed therefore to be equal to 0.3A

Effect of the pH
It has been established that the pH is one of the most significant factors affecting the performance of the electrochemical process, particularly on the performance of the electrocoagulation process.To evaluate its effect, a series of experiments were performed, using 50 mg/L amoxicillin for initial pH in the range 2 to 10.As illustrated in Fig. 5, the removal efficiency of amoxicillin remained constant and close to 99% for pH in the range 4 to10, and decreased to 10 % for pH 2. The effect of pH can be explained considering aluminum and AMX equilibrium related to pH.At low pH, such as 2-3, cationic monomeric charged and are therefore strongly adsorbed onto the organic anionic particle and become insoluble by hydrolyzed cationic species such as Al(OH)2 + and hence are more strongly adsorbed on negative surface than the free hydrated metal ion.At pH greater than 7.7, AMX prevails as a monovalent anion, +-or a divalent anion 0-, from the loss of protons from the carbonyl system and phenolic diketone moiety.The high removal efficiency can be assigned to the double effects of the attracted force between the cationic species of Al3+ and anionic species of AMX and the adsorption of this latter onto Al(OH)3, which presents a large surface area.These flocs are active leading to a rapid adsorption of soluble organic compound (and trapping of colloidal particle) and are easily separated from aqueous medium by sedimentation or H2 flotation.The surface complexes of zwitterionic species of AMX were previously suggested by Figueroa et al. as the major contributor to the adsorption mechanism of a kaolinite, montmorillonite.These results were also reported by Chen et al who studied the adsorption and transformation of antibiotics onto aluminum oxide.

Effect of the initial AMX concentration
The initial concentration provides an important driving force to overcome all mass transfer resistances of solutes between the aqueous and the solid phase.The effects of the initial concentration (10-300 mg/L) were investigated at constant current intensity 0.8 A with1.25 g/L KCl in each experiment.The temperature of AMX solution was maintained at 20°C and the EC experiments were run each time for about 15 min.The effect of the initial concentration on the removal yield is displayed in Fig. 6, showing that the removal efficiency (RE) decreased almost linearly for increasing AMX concentrations.The highest RE (96.5%) was obtained after only 2 min at 10 mg/L, while the lowest RE (50%) was obtained at 300 mg/L.Lower RE at higher AMX concentration was caused by a lower amount of coagulant, Al(OH)3 species, which became therefore limiting.

Isotherm modeling
Analysis of the experimental adsorption data was carried out by considering the Langmuir, Freundlich, Sips and Toth isotherms.The applicability of these isotherms was compared using the correlation coefficient R2.The values for the constants q0, b, Kf , n and m of the isotherms are collected and based on the R2 values, it can be noticed that the considered adsorption isotherms matched experimental data in the following increasing order: Sips > Toth > Langmuir > Freundlich isotherms.The above order revealed that the equilibrium data are better fitted by threeparameter models than two-parameter models.The Sips model was found to be the most relevant to represent equilibrium data, showing that adsorption was heterogeneous and assumed a quasi-Gaussienne distribution energy owing to the high R2 value also found for the Toth model.

Kinetic studies
Pseudo-first, pseudo-second, Elovich and fractional Power models have been considered to describe experimental data and the corresponding correlation coefficients are given in Table 2.As shown, for all studied parameters the correlation coefficients for the first-order, Elovich and Power function kinetic models were relatively lower than those obtained for the second-order kinetic model for the various current densities, pH and initial AMX concentrations considered.These results indicate that the second-order kinetic model can be suitably applied to predict the amoxicillin adsorption process onto aluminum hydroxides.This model supposes that two reactions either in series or in parallel occur; the first one is fast and reaches equilibrium quickly and the second is a lower reaction that can continue for a long period of time.It has been observed above that the operating parameters have a significant influence on the rate constant K2 of the pseudosecond order model (Eq.9).Fig. 7a shows the influence of pH on the rate constant.It can be ascertained that the rate constant remained constant for pH values in the range of 4-10, similarly to the pH effect on AMX removal yields.The effect of the initial concentration on the rate constant shows that the reaction rate constant (K2) decreased significantly for increasing initial AMX concentrations (Fig. 7b).This may be due to the fact that for a given charge, the number of hydroxides flocs generated was insufficient and an increase in the ratio of the initial concentration to the amount of flocs generated resulted in a reduction of the yield of AMX removal.The effect of the current intensity on the rate constant shows an increase for increasing current intensities (Fig. 7c).This may be explained by the fact that for a given amount of pollutant, the amount of Al(OH)3 generated increased with the current intensity.

CONCLUSION
This work was a first step to improve the knowledge regarding the process removal by electrocoagulation with aluminum electrodes.The EC method applied in this study provided a sensitive, rapid and reliable technique for the removal of AMX.The use of aluminum as sacrificial electrodes in the treatment of synthetic AMX solutions by electrocoagulation has been found to be dependent on pH, current intensity and initial concentration.By applying linear methods, the mechanism of EC was modeled using pseudo-first, Elovich, Power Function and pseudo-second order models and it was shown that the EC kinetic followed pseudo-second order kinetic and that the reaction rate constant was influenced by the operating parameters.The metal hydroxides generated by EC can efficiently remove amoxicillin by adsorption, and the EC process was modeled using adsorption isotherm models, showing that the Sips model accurately described experimental data.The results obtained in this study appear promising for the application of EC technology for the treatment of waters loaded with antibiotics, such as amoxicillin (AMX).For this purpose, they should be subsequently confirmed on real effluent.