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Annals of Chromatography and Separation Techniques

Adsorption Performance of Laccase Modified-Red Mud for Acid Fuchsin Dye Removal from Aqueous Solutions

[ ISSN : 2473-0696 ]

Abstract Citation Introduction Material and Methods Results and Discussion Conclusion Acknowledgement References
Details

Received: 09-Dec-2016

Accepted: 09-Jan-2017

Published: 12-Jan-2017

Hayrunnisa Nadaroglu¹,², Ekrem Kalkan³, and Neslihan Celebi⁴*

¹ Department of Food Technology, Ataturk University, Turkey
² Department of Nano-Science and Nano-Engineering, Ataturk University, Turkey
³ Department of Geological Engineering, Ataturk University, Turkey
4 Department of Chemical Technology, Ataturk University, Turkey

Corresponding Author:

Hayrunnisa Nadaroglu, Department of Nano-Science and Nano-Engineering, Ataturk University, Turkey, Tel: 0-90 442-2311818; Fax: +90-442-2360982; Email(s): Hnisa25@yahoo.com, Hnisa25@atauni.edu.tr

Keywords

Acid Fuchsin dye removal; Red mud; Laccase from Russulaceae (Lactariusvolemus); Adsorption isotherms; Adsorption kinetics; Thermodynamic parameters

Abstract

One of the powerful treatment processes for the removal of dyes from aqueous solutions is adsorption method. In this study, removal of Acid Fuchsin dye from aqueous solutions has been studied by using Red Mud (RM) waste material after its modification with laccase from Russulaceae (Lactariusvolemus). Laccase was purified by using saturated precipitate (NH4 )2 SO4 , DEAE-cellulose and immobilized on red mud. Batch adsorption experiments have been performed as a function of pH, contact time, temperature, and adsorbent dosage. The Freundlich equation was found to have the highest value of correlation coefficient compared with the Langmuir model. In addition, pseudo-first-order and pseudo-second order models were used to study the kinetics of Acid Fuchsin dye adsorption onto RM and laccase modified-RM. It was proved that adsorption process undergoes pseudo-second-order kinetic by the high value of correlation coefficient. Thermodynamic parameters including the Gibbs free energy, enthalpy and entropy changes indicated that the adsorption of Acid Fuchsin dye onto laccase modified-red mud was feasible, spontaneous and endothermic. The results show that the laccase modified red mud can be used for the treatment of aqueous solutions as an alternative low cost adsorbent.

Citation

Nadaroglu H, Kalkan E and Celebi N. Adsorption Performance of Laccase Modified-Red Mud for Acid Fuchsin Dye Removal from Aqueous Solutions. Ann Chromatogr Sep Tech.2017;3(1):1027.

Introduction

The conventional treatment methods for dye removal, such as chemical coagulation, activated sludge, biodegradation, oxidation, membrane separation, adsorption and photo degradation, have been extensively explored [1-3]. Among the physical and chemical processes, the adsorption procedure is effective in producing high-quality effluent without the formation of harmful substances [4-7]. However, low-cost adsorbents with high adsorption capacities are still being developed to reduce the adsorbent dose and minimize the problem of disposal. Significant attention has been directed toward various adsorbent materials, which may be obtained in significant quantities and are nontoxic to nature [8-9].

As an alternative low-cost absorbent material, solid wastes are generally used as adsorbent for the removal of heavy metals and dyes from wastewater. One type of solid waste material,Red Mud (RM) is largely produced by the alumina industry. It emerges as a by-product of the caustic leaching of bauxite to produce alumina.The RM is principally composed of fine particles of silica, aluminum,iron,calcium,and titanium oxides and hydroxides, which are responsible for its high surface reactivity [10-12].

The RM waste material was used, as low-cost adsorbent material after its modification with laccase from Russulaceae (Lactariusvolemus). It is an enzyme and belongs to those enzymes, which have innate properties of reactive radical production.There are diverse sources of laccase producing organisms like bacteria,fungi and plants. Laccases use oxygen and produce water as by product.They can degrade a range of compounds including phenolic and non-phenolic compounds.They also have ability to detoxify a range of environmental pollutants [9].

This paper describes the use of RM and laccase modified-RM for removal of Acid Fuchsin Dye (AFD) from aqueous solutions.The adsorption of AFD has been investigated as a function of pH, contact time, temperature, and adsorbent dose.Adsorption isotherm,kinetic and thermodynamic studies have been performed to describe the adsorption process.

Material and Methods

Acid Fuchsin dye (AFD)

The AFD, 2-amino-5-[(4-amino-3-sulfophenyl) (4-imino-3-sulfo-2,5-cyclohexadien-1-ylidene)-methyl] -3-methylbenzenesulfonic acid, is an organic dye (C.I.42685) and has a formula,C2 0H17 N3 Na2 O9 S3 .Its molecular structure is given in Figure 1.

Figure 1: Chemical structure of Acid Fuchsin dye (AFD).

This organic dye is also called as Acid Violet 19 or Fuchsin Acid or Rubin S and is widely used for staining procedures [13] and other purposes [14].

Red mud

The red mud material emerges as unwanted by-products during alkaline-leaching of bauxite in Bayer process.The alkaline RM-water pump has been dumped annually into specially constructed dams around the Seydisehir Aluminum Plant, Konya (Turkey). RM used in this experimental study has been obtained from this plant. Its physical properties, chemical constituents and mineralogical composition are given in Table 1.

Table 1: Physical properties, chemical constituents and mineralogical composition of R.

Property Value Constituents Value Minerals Value
Density (mg/m3) 28.5 Al2O3(%) 20.2 Sodalite(%) 32.2
Specific gravity 3.05 Fe2O3(%) 35.04 Cancrinite(%) 4.6
    CaO(%) 5.3 Hematite(%) 34.7
    MgO(%) 0.33 Diaspore(%) 2.6
    TiO2(%) 4 Rutile(%) 1.6
    Na2O(%) 9.4 Calcite(%) 1.3
    SiO2(%) 17.29    
    Ignition(%) 8.44    

Laccase enzyme

Laccase is an enzyme that has potential ability of oxidation. There are diverse sources of laccase producing organisms like bacteria, fungi and plants [9]. Lactariusvolemus is a species of mushroom in the family Russulaceae. It is widely distributed in Erzurum (Turkey). As a mycorrhizal fungus, its fruit bodies grow on the ground at the base of various species of trees in the summer and autumn in broad-leaved forests,either individually or in groups. It is valued as an edible mushroom and not toxic. Also,Lactariusvolemus has antioxidant, antiradical and antimicrobial activities [15].

Purification of laccase enzyme

Lactariusvolemus (10 g) was ground in liquid N2 and homogenized in a blender with 50 cm3 of 1 M KCl by shaking, and centrifuged at 5.000xg for 60 min. The homogenates were centrifuged and precipitates were removed. For the purification of the laccase enzyme,the following procedure was implemented [15]. Laccase was purified from the supernatant in two steps. Firstly, it was partially purified by precipitation in (NH4 )2 SO4 .Secondly, ion exchange chromatography on DEAE-sephadex was used.The collapse of (NH4)2 SO4 was done from 0 to 90% in supernatant with the internals of 0-10,10-20,20-30,30-40,40-50,50-60,60-70, 70-80 and 80-90%. Significant activity was not observed below a range of 0-40% (NH4)2 SO4 .The majority of activity was found in the 40-60% precipitate. Solid (NH4)2 SO4 was added to the supernatant to increase the concentration of (NH4)2 SO4 from 40% of the fraction to 60%. After, mixing it in an ice-bath for 1h with magnetic stirring, it was centrifuged (10.000xg,30 min,and 4°C).The supernatant was discarded and the precipitate was dissolved in 0.01 M acetate buffer (pH 5.0) and dialyzed against the same buffer [15-16].

Adsorbent preparation for experimental study

The RM was thoroughly washed with distilled water until it became neutral. The suspension was wet sieved through a 200-mesh screen.A little amount of the suspension remained on the sieve and was discarded. The solid fraction was washed five times with distilled water following the sequence of mixing,settling, and decanting. The last portion of suspension was filtered, and the residual solid was then dried at 105°C, ground in a mortar, and sieved through a 200-mesh sieve.Laccase from Russulaceae (Lactariusvolemus) was purified by using precipitate of saturation (NH4)2SO4 ,DEAE-cellulose and immobilized on RM.1 g of RM sample was shaken with 10 cm3 (5 mg protein/cm3) laccase from Lactariusvolemus solution for approximately 1h, and then the separated particles were stored.

Material characterization

The Scanning Electron Microscope (SEM) was used to examine the surface of the adsorbent. Images of native adsorbent and dye loaded adsorbent were magnified 5000 times by SEM modeled JEOL JSM-6400 SEM. In addition, the Fourier Transform Infrared Spectroscopy (FTIR) analyses were carried out to identify functional groups and molecular structure in the laccase-modified RM and AFD loaded laccase-modified RM. FTIR spectra were recorded on the on Perkin-a Perkin-Elmer GX2000 FTIR spectrometer. The spectrum of the adsorbent was measured within the range of 4000 and 700 cm-1 wave number.

Adsorption procedure

All studies were made in a 50 cm3 stoppered Erlenmeyer flaks filled with AFD from 50 mg/dm3. The Red Mud was added to dye solution in the amount from 0.125 to 2g red mud. The pH was adjusted to the desired value by using 0.1 M NaOH or 0.1 M HCl. Then, the glasses were placed in a shaker at the room temperature. The agitation was provided at 500rpm and 15 min to reach the equilibrium state. The samples were taken out from the flaks periodically by using a micropipette. Then the reaction mixtures were centrifuged at 5000 rpm for 10 min. Upper solution was filtered using 0.45 µm filters. The concentration of AFD was measured using a spectrophotometer set at 545 nm.

Calibration curves were established prior to the analysis. A calibration curve was prepared in the range 0-40 ng/cm3 of AFD according to the general procedure.The obtained absorbance values from the samples were substituted in the equation of the calibration curve and the concentration of the dye in the samples was found.

The amounts of the dyes adsorbed onto adsorbent (qe in mg/g) and the percentages of the dyes were calculated from the equations:

whereCo and Ce are the initial and equilibrium concentrations of AFD in solution (mg/dm3);V is the volume of solution (dm3) and m is the mass of adsorbent (g).

Results and Discussion

Red mud characteristics

FT-IR spectra: The functional groups and surface properties of the native adsorbent and after adsorption by FT-IR spectra were illustrated in the Figure 2 (a-b).

Figure 2: FT-IR spectrum of adsorbent (a) and adsorbent loaded with AFD (b).

The strong bands between 3270-3543 cm−1 express hydroxyl-stretching region. This state has become more pronounced after AFD absorption and it express that there is water in RM. The peak around 1646.17 cm−1 is attributed to water molecules absorbed into alumina silicate structure [17]. The absorption bands of carbonates incorporated in the main channel of can crinite were appeared between 1409.79-1473.51 cm−1 regions in the samples.The peak around 1410 cm−1 belongs to NO-group within can crinite and sodalite (Table 1). Another peak around 959.44 cm-1 belongs to stretching vibrations of Si(Al)–O structure. To evaluate, through the FTIR technique, the interaction mechanisms between the AFD and RM, we focused our attention on a part of the mid infrared region, 629-644 cm−1, where bands associated with various AFD–O(H) stretching vibrations were found.

SEM study: The photography has been a primary tool for characterizing the surface morphology and fundamental physical properties of the adsorbent surface. The SEM is useful for determining the particle shape, porosity and appropriate size distribution of the adsorbent [18]. The SEM images of modified-RM and AFD adsorbed laccase modified-RM are shown in Figure 3 (a-b).

Figure 3: SEM images of RM (a) and AFD loaded laccase modified-RM (b).

It is clear that, RM has considerable numbers of pores where, there is a good possibility for dyes to be trapped and adsorbed into these pores. Based on analysis of the images taken by SEM before and after the dye adsorption process, highly heterogeneous pores within RM particles were observed. After adsorption process, the pores were packed with AFD and this finding revealed the coverage of the modified natural material surface with molecular cloud of dye [18].

Adsorption study

Effect of pH: The effect of initial pH on removal of the AFD onto RM and laccase modified-RM is shown in Figure 4.

Figure 4: Effect of pHon the removal of AFD by RM and laccase modified RM initial (AFM concentration:50 mg/dm3,red mud dose:1 g/50 cm3, agitation speed:500 rpm and temperature: 30±1°C).

The optimum pH, at which the maximum removal occurred, was obtained at pH 6 and pH 5 for RM and laccase modified-RM, respectively.This is due to the surface complexation reactions, which are mostly influenced by the electrostatic force of attraction between AFD and the surface of the adsorbent.The acidity of the medium can affect the AFD ions’ uptake amount of the RM and laccase modified-RM adsorbents because hydrogen ions in the solution could compete with AFD for active sites on the adsorbent surface [19]. At lower pH values,the amount of dye adsorbed decreased due to repulsive force between positively charged surface and the positively charged dye molecules.When the pH of the solution is increased,the positive charge on the solution interface decreases and the adsorbent surface becomes negatively charged. Change of pH affects the adsorptive process through dissociation of functional groups on the adsorbent surface active sites [20].

Effect of contact time: The effect of contact time on removal of the AFD onto RM and laccase-modified RM absorbents was shown in Figure 5.

Figure 5: Effect of contact time on the AFD concentration (Ct) after adsorption on RM and laccase modified-RM (pH:5.0, initial AFM concentration:50 mg/dm3,red mud dose:1 g/50 cm3,agitation speed: 500 rpm and temperature: 30±1°C).

The removal of AFD increases with time in the first 45 min for laccase modified-RM.Basically, the removal of AFD was rapid at this time but it gradually increases with time until it reaches equilibrium. At the first 45 min of contact time, the concentration of AFD molecules in aqueous solution reached 2.35 mg/dm3 and 2.46 mg/g was adsorbed by laccase-modified RM at the equilibrium state. Also,at 90th min of contact time, the adsorption rate was reached to 2.32 mg/g and 2.41 mg/g for RM and modified RM, respectively.

For the laccase-modified-RM adsorption, rapid adsorption and equilibrium in a short period of time is related to the efficacy of the adsorbent, especially for waste water treatment [21-22]. The rapid removal of the adsorbate has significant practical importance as it facilitates smaller reactor volumes ensuring efficiency and economy [19-23].

Effect of temperature: The effect of temperature on the adsorption of AFD by RM and laccase-modified RM absorbents was illustrated in Figure 6.

Figure 6: Effect of temperature on the removal of AFD by RM and laccase modified-RM (pH:5.0,initial AFM concentration:50 mg/dm3,red mud dose:1 g/50 cm3,agitation speed: 500 rpm.

The maximum removal amount of adsorbate was 2.480 mg/g for RM at 40°C and 2.487 mg/g for laccase modified-RM at 40°C. A temperature increase can lead to a rise in kinetic energy and mobility of dye molecules, and can also cause an increase in the intra-particle diffusion rate of the adsorbate.This increase also affects the solubility and chemical potential of the adsorbate, possibly becoming a factor that controls adsorption [24]. Since adsorption is an exothermic process, it would be expected that an increase in temperature of the adsorbate-adsorbent system would result in decreased adsorption capacity.Thus,the adsorption of AFD leads to a decrease in the residual forces on the surface of adsorbent and hence causing a decrease in the surface energy of the adsorbent [25].

Effect of adsorbent dosage: The effect of RM and laccase modified RM dosage on amount of AFD adsorbed was shown in Figure 7.

Figure 7: Effect of adsorbent dosage on the removal of AFD by RM and laccase modified-RM (pH: 5.0,initial AFM concentration: 50 mg/ dm3, agitation speed: 500 rpm and temperature: 30±1°C).

The maximum amount of AFD adsorbed was 23.85 and 24.80 mg/g for AFD attained for adsorbent dose of 1g/50 cm3 for RM and laccase modified-RM, respectively. Increase in adsorbent dosage increased the amount of dye removal, which is due to the increase in contact surface area of the adsorbent [26]. Increase in adsorption efficiency with increase in adsorbent dosage is attributed to the increase of active sites for adsorption of dye molecules. At very low adsorbent concentration, the adsorbent surface becomes saturated with the dye and the residual dye concentration in the solution is too high [27].

Effect of initial dye concentration:The effect of initial dye concentration on the adsorption was also studied at different concentrations of dye (1.25,2.5,5,10,20 and 25 mg / dm3) at initial pH value 5.0 and temperature 30±1°C. The Figure 8 shows the effect of initial dye concentration on the amount of dye adsorbed.

Figure 8: Effect of AFD concentration on the removal of AFD by RM and laccase modified-RM (pH:5.0, agitation speed: 500 rpm and temperature: 30±1°C).

The amount adsorbed was greater for higher initial dye concentration for RM and laccase modified-RM. The amount of AFD adsorbed, in equilibrium state, increased from 1.23 to 20.94 for RM and from 1.24 to 24.94 mg/g for laccase modified-RM when the initial dye concentration increased from 1.25 to 25 mg/dm3, respectively.

At higher initial concentrations, the resistance to mass transfer between the solid and aqueous phase is more easily overcome due the driving forces, moreover the number of collisions between dye molecules and adsorbent is increases, increasing the adsorption [28].

Adsorption isotherms

Langmuir adsorption isotherm model: The Langmuir isotherm is derived on the assumption that adsorption occurs at specific homogenous sites within the adsorbent. The liner form of the Langmuir isotherm equation is given as:

(Where qmax (mg/g) and b (dm3/mg) are Langmuir constants which are indicators of the maximum adsorption capacity and the affinity of the binding sites, respectively.They can be determined from a linear form of Eq. 3 (by plotting the Ce/qe versus Ce), represented by the following equation:

The values of qmax and b were calculated from the slope and intercept of the Langmuir plot of Ce /reverses Ce from Figure 9a.

Figure 9: Langmuir (a) and Freundlich (b) adsorption isotherm.

The empirical constants qmax and b for laccase modified-RM were found to be 233.33 mg/g and 134.67 dm3/mg (Table 2) respectively. The applicability of the linear form of Langmuir model to RM and laccase modified-RM was proved by the high correlation coefficients R2 (0.9576 and 0.9608, respectively)>0.95. These suggest that the Langmuir isotherm provides a good model of the sorption system.

Table 2: Values of the Langmuir and the Freundlich adsorption isotherm models.

Langmuir adsorption model Freundlich adsorption model
Langmuir RM Laccase Freundlich RM Laccase
constants modified-RM constants modified-RM
qmax (mg/g) 250 333.33 KF(mg/g) 0.052 0.052
b (dm3/mg) 123.25 134.67 n 0.599 0.615
R2 0.9576 0.9608 R2 0.9945 0.9697

Freundlich adsorption isotherm model: The Freundlich isotherm model is an empirical relationship describing the adsorption of solutes from a liquid to a solid surface and assumes that different sites with several adsorption energies are involved. It is described by applying the following equation:

Where KF and n are the Freundlich constants related to the sorption capacity of the adsorbent (mg/g) and the energy of adsorption, respectively. They can be calculated in the following linear form;

KF and n values were calculated from the intercept and slope of the plot (Figure 9b). In the literature, it is pointed out that the parameters, KF and n affect the adsorption isotherm. For RM and laccase modified-RM, based on the high correlation coefficients R2 (0.9945 and 0.9697 respectively) > 0.95, it has been deduced that Freundlich model better fitted to the experimental data (Table 2).

Adsorption kinetic models

The pseudo-first-order kinetic model: The linearized form of pseudo-first-order kinetic model can be written as [29]:

Where k1 is the pseudo-first-order rate constant (min-1), qt and qe are the amounts of AFD adsorbed at time t and at equilibrium (mg/g). At different dye concentrations, the correlation coefficients and k1 were calculated for AFD adsorption from the linear plots of log (qe-q t) versus t for RM and laccase modified-RM (Figure 10).

Figure 10: Pseudo-first-order reaction for AFD adsorbed onto RM and laccase modified-RM adsorbents at different dye concentrations.

The results were presented in Table 3.The plots of Eq.7 show lower correlation coefficient values and the qe-cal values of pseudo-first-order equation are found to be lower than the experimental one. This indicates that pseudo-first-order model is not suitable to describe kinetic data.

Table 3: Kinetic parameters for the adsorption of AFD.

Initial AFD concentration (mg/dm3)   Pseudo-first-order rate equation Pseudo-second-order rate equation
qe-exp (mg/g) k1 qe-cal (mg/g) R2 k2 qe-cal (mg/g) R2
RM adsorbent 2.48 0.014 1.24 0.9265 0.82 2.19 0.9833
5
25 14.2 0.033 13.67 0.9362 4.7*10-3 19.49 0.9174
50 19.4 0.038 13.65 0.9018 1.2*10-3 21.37 0.9855
Laccase modified-RM adsorbent 2.48 0.034 1.66 0.8323 0.645 2.64 0.9636
5
25 17.1 0.035 16.12 0.9573 2.7*10-3 21.74 0.9404
50 23.4 0.038 13.79 0.9476 5.72*10-4 24.063 0.9927

The pseudo-second-order kinetic model: The pseudo-second-order kinetics can be written as follows [22]:

Where the equilibrium rate constant of pseudo-second-order model is k2 here (g mol-1 min-1).This equation has been applied to the current study on AFD adsorption. At different dye concentrations, the correlation coefficients, qe and k2 were calculated for AFD adsorption from the linear plots of t/qt versus t for RM and laccase modified-RM (Figure 11).

Figure11: Pseudo-first-order reaction for AFD adsorbed onto RM and laccase modified-RM adsorbents at different concentrations.

The results were presented in Table 3. The correlation coefficients of the pseudo-second order kinetic models are closer to unity and the calculated qe values computed from pseudo-second order equation show good agreement with experimental values. This indicates that the pseudo-second-order kinetic model is applicable for the adsorption of AFD onto RM and laccase modified-RM.

Adsorption thermodynamics

The aim of thermodynamic study is to establish the thermodynamic parameters that can characterize the adsorption process of AFD onto the RM and laccase modified-RM. The adsorption capacity of laccase modified-RM adsorbent increased with increase in the temperature of the system from 293 to 303 K. Thermodynamic parameters such as change in free energy (ΔGo) kJ/mol, enthalpy (ΔHo) kJ/mol, and entropy (ΔSo) J/Kmol were determined using the following equations [30]:

Where KL is the equilibrium constant, Cs is the solid phase concentration at equilibrium (mg/dm3), Ce is the liquid phase concentration at equilibrium (mg/dm3), T is the temperature in Kelvin, and R is the gas constant. ΔHo and ΔSo values are obtained from the slope and intercept of plot ln KL against 1/T. Van’t Hoff plot of the temperature effect on adsorption of AFD onto the RM and laccase modified-RM was illustrate in Figure 12 and the observed thermodynamic values were summarized in Table 4.

Figure 12: Influence of temperature on thermodynamic behavior of AFD for RM and laccase modified-RM.

Table 4: Thermodynamic parameters for the AFD adsorption.

  Thermodynamic parameters
Temperature (K) ΔGo(kJmol-1) ΔHo(kJmol-1) ΔSo (Jmol-1)
RM adsorbent -35150.1    
293 -35750.3 24.58 120.05
298 -36350.6    
303      
Laccase modified-RM adsorbent -33739.4    
293 -34315.6 22.97 115.23
298 -34891.7    
303      

The ΔG° values decrease with an increase in temperature, indicating an increased trend in the degree of spontaneity and feasibility of AFD adsorption. In the case of AFD adsorption onto RM and lacc(NH4)2 SO4 ase modified-RM, the values of Gibbs free energy of the process at all temperatures are negative. The negative value of ΔG° indicates the adsorption is favorable and spontaneous. The ΔG° values are found to decrease as the temperature increases in both dye-anion exchanger systems suggesting that higher temperatures make the adsorption easier [31]. For the RM and laccase modified RM, the ΔH° and ΔS° have positive values. The positive values of ΔH° further confirm the endothermic nature of adsorption process. The positive values of ΔS° indicate good affinity of the anion exchangers for AFD molecules and show increase in the degree of freedom for the adsorbed species [32-35].

Conclusion

In this study, red mud (RM) and laccase modified-RM were used as low-cost absorbent materials and the suitability of the activated RM for adsorption of Acid Fuchsin dye (AFD) from aqueous solutions was investigated. The results indicate that RM and laccase modified-RM can be successfully used for the adsorption of AFD from aqueous solutions. The results showed that laccase modified-RM was more applicable for the AFD adsorption compared with RM. The pH, adsorbent dose, contact time and temperature affected the adsorption process. For the laccase modified-RM, the optimum values were obtained at pH 5, contact time of 45 min, temperature of 60°C and an adsorbent dose of 1 mg/dm3. The Freundlich equation was found to have the highest value of correlation coefficient compared with the Langmuir model. The kinetics of the adsorption of AFD reports to be pseudo-second-order chemical reaction kinetics. Thermodynamic parameters including the Gibbs free energy, enthalpy and entropy changes indicated that the adsorption of AFD onto laccase modified-RM adsorbent was feasible,spontaneous and endothermic. Based on the results,RM and laccase modified-RM can be used as a relatively efficient and low cost absorbent for the removal of AFD dye from aqueous solutions. However, the maximum adsorption capacity (qmax) values showed that laccase modified-RM was as a better adsorbent for remediation of AFD from aqueous solutions.

Acknowledgement

This research has been performed under the project numbered 2011/80 and supported by the Research Development Center of Ataturk University.The authors acknowledge the support of Ataturk University,Turkey for this work.

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Other Articles

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Removal of Acid Beverage Flocs in Crystal Sugar by Adsorption Column Chromatography: Preliminary Study with Adsorbent Resin

The sugar industry has been facing some problems with white sugar intended for soft drinks production. Some studies have been demonstrated the sugar could be source of insoluble substances technically called by Acid Beverage Flocs (ABF). It appears during the beverage production; however, the flocs are easily disappearing with shaking. This may be related to raw material the sugarcane quality and, consequently, with the efficiency of the juice clarification process, since if there is no adequate juice treatment. The sugarcane commonly has lower quality and higher intensity of impurities, such as proteins, wax, minerals and colloids. The sugar industries are implementing solutions to reduce the amount of impurities through using technologies like ionic resins to removal of color, odor or undesirable taste. It could transform raw sugar in refined or white sugars. The aim of this work was evaluate the efficiency of purification of sugar solution with chromatographic adsorption system. We observed that the color reduction was around 69% and an intensive reduction in turbidity of sugar aqueous solution. There were variation on sucrose and increase on reducing sugars (glucose and fructose) contents. It is possible to conclude that the process could be efficient to reduce the color (MAU color), turbidity and ABF into sugar solutions.

Roberta Bergamin Lima and Claudio Lima de Aguiar*


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A Study to Evaluate Aflatoxin Contamination in Food from Gauteng Province

Aflatoxins (AFs) and their producers have been found to be problematic and is still an issue. This is due to their role in influencing food quality, health and economy loss. In maintaining good food quality, minimize AFs occurrence and its deleterious effects, it is essential that issues relating to mycotoxin production and contamination are monitored, and addressed on a regular basis. This will proffer suggestions for immediate actions to be taken, in order to achieve and maintain regulatory limit before situations are out of control. Hence the case study to evaluate the concentration of AFs in food, by way of thin layer chromatography and high performance liquid chromatography was attempted. This is to monitor concentrations of the emerging mycotoxin in relation to international regulatory limits. Concentrations levels ranging 0.06 - 77.97 ppb was observed, (mean: 16.8 ppb) and measured out in the food samples of study, exceeding the ISO limits (0.05 ppb). This calls for proper monitoring of pre and postproduction stages in food, by employing easy to use chromatographic techniques as a routine process to screen and ascertain concentrations do not exceed regulatory limits.

Henry E Iheanacho¹,²,³*


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Investigation of Naturally Occurring Fumonisin B1 and Glycated Fumonisin B1 in Korean Feedstuffs

Mycotoxins are potentially dangerous contaminants of livestock feeds. In this study, we measured the levels of fumonisin B1 and glycated fumonisin B1 in feedstuffs and then investigated the ability of the extrusion heating regimen to convert the most prevalent mycotoxin contaminant, fumonisin B1 , to a less toxic glycated form. All feed samples were analyzed with fully validated methods. All measured concentrations of fumonisin B1 were below harmful thresholds, including European Union-recommended levels or US Food and Drug Administration action levels.

Because fumonisin B1 was highly contaminated mycotoxin in our present investigation and fumonisin B1 has been shown to be less toxic following Maillard type reaction with reducing sugar, we examined the formation of fumonisin B1 derivatives by Maillard reaction under extrusion process conditions. We employed a variety of tandem mass spectrometric methodologies to selectively detect fumonisin B1 derivatives and to elucidate their structures partially. We found that compounds of m/z 736 were more likely artifacts or side reaction products rather than glycation products. N-(carboxymethyl) fumonisin B1 of m/z 780 and other major glycation products of m/z 794 and 810 were not detected, and only negligible amounts of methylene fumonisin B1 was found in 10 extruded feed samples. Therefore, either the tested extrusion conditions did not induce fumonisin B1 glycation or the glycation products simply could not be detected by the method employed in this study.

Jongsung Ahn¹, Hyenjong Kim¹, and Kwang-Yeop Jahng²*


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Determination of HMF in Some Instant Foods and Its Biodegradation by Some Lactic Acid Bacteria in Medium and Food

The aims of this study were to determine HMF level in some foods and to reduce their level by biodegradation. Coffee whitener, cappuccino, hot chocolate, instant coffee, instant powdered mix (coffee, coffee whitener and sugar) and aromatized cocoa were subjected to HMF analysis in the scope of this study. The HMF determination of samples was carried out using a high performance liquid chromatography. Color properties of the samples were determined according to standard procedures and their relations with HMF content were also investigated. The biological degradation of HMF with lactic acid bacteria was also studied with broth media and a model food system (reconstituted milk).The average HMF levels were 12.59 mg/kg for coffee whitener, 572.49 mg/ kg for cappuccino, 660.29 mg/kg for hot chocolate, 1804.91 mg/kg for instant coffee, 871.56 mg/kg for instant powdered mix and 980.94 mg/kg for aromatized cocoa. The addition of lactic acid cultures reduced the HMF content of the samples. HMF levels of broth media and model food inoculated with lactic acid bacteria (L. lactis, L.bulgaricus, L. cremoris) decreased about 25 % as a result of HMF biodegradation.

Rasim Alper Oral¹, Mahmut Dogan², Kemal Sarıoglu², Ahmed Kayacıer¹, and Osman Sagdic³*


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An Integrated Analysis of the Musa Paradisiaca Peel, Using UHPLC-ESI, FT IR and Confocal Microscopy Techniques

When the banana (Musa paradisiaca) peel was subject of enzymatic hydrolysis with cellulase and hemicellulase, only glucose was obtained. Images from banana peel, using confocal laser scanning microscopy, demonstrate that the cellulose is the main structural compound. Fatty acids, phenolic and other compounds were detected from the organic residual extract, and characterized by means of NMR, FT-IR and UHPLC-MS techniques. The presences of these compounds were corroborated through a steam distillation. Under this condition, banana peel could have potential applications in the food field, where could be used to improve some procedures such as the obtaining of banana vinegar.

Miriam Alejandra González Corona¹, Mayra Beatriz Gómez-Patiño², María de Jesús Perea Flores², Luis Alberto Moreno Ruiz², Blanca Margarita Berdeja Martinez¹, and Daniel Arrieta-Baez²*


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Structural Characterization of Bamboo Lignin Isolated With Formic Acid and Alkaline Peroxide by Gel Permeation Chromatography and Pyrolysis Gas Chromatography Mass Spectrometry

Fractionation is an effective technology to maximize the utilization of lignocelluloses for the production of chemicals and materials. In this case, bamboo was subjected to a two-step fractionation process based on the concept of biorefinery: (a) formic acid treatment at boiling point under atmospheric pressure for 2 h, and (b) post treatment with alkaline hydrogen peroxide solution containing 1% NaOH and 1% H2 O2 at 80 ºC. The combination of formic acid delignification and alkaline hydrogen peroxide degradation achieved an effective removal of both lignin (delignification rate 94.9%) and hemicelluloses (removal rate 87.4%) from bamboo, producing cellulose rich pulp, formic acid lignin and sugars. To investigate the structural modification of lignin during the fractionation process, the residual lignin in the treated samples was isolated and characterized with multiply techniques including gel permeation chromatography, pyrolysis gas chromatography mass spectrometry, Fourier-transform infrared spectroscopy, etc. The relative ratio of S/G was 1.63 for bamboo milled wood lignin (L1), whereas the lignin isolated from the formic acid treated cellulose-rich fraction (L2) presented a chromatograph similar to that of L1 but had a lower S/G ratio of 1.28. This indicated that a preferential removal of S units during the formic acid fractionation process. In addition, alkaline hydrogen peroxide treatment resulted in more removal of S units, as indicated by a lower S/G ratio of 0.71.

Xun Li¹, Chang-Zhou Chen¹, and Ming-Fei Li¹*

 


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Volatile Compound Profiles by HS GC MS for the Evaluation of Postharvest Conditions of a Peach Cultivar

Volatile Organic Compounds (VOCs) profile of foods obtained by Gas Chromatography/Mass Spectrometry (GC/MS) can be considered a potent tool of food products quality changes occurring as a result of different processing, such as ripening and deterioration. The aim of the present study was the evaluation of volatiles profiles of peaches (cv Springcrest) during their storage in conditions similar to those of long distance transport that normally these products undergo before being placed on market. We investigated control sample (no stored fruit) and peaches stored in cardboard boxes wrapped in heat-sealed HD polythene bags, both in normal and modified atmosphere (0% and 23% CO2 ) after 1 and 8 days of storage at 4°C. GC/MS analysis of these samples allowed the identification of a total of 115 VOCs.

The comparison of the VOCs profile of the three peach samples (control, normal atmosphere and 23% CO2 ) shows that fruits packaged in normal atmosphere released a greater amount of esters of medium chain fatty acids, such as ethyl nonanoate and ethyl dodecanoate. On the other hand, fruits stored in normal atmosphere and modified atmosphere after 8 days of storage (increased concentration of CO2 in packs) released a greater amount of esters of long chain fatty acids, such as ethyl hexadecanoate.

Livia Malorni¹, Antonella Martignetti¹, and Rosaria Cozzolino¹*


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Current Trends in Lignocellulosic Analysis with Chromatography

The conversion of lignocellulosic biomass into biofuel and biomaterial is promising for the substitution of fossil resources in energy and material applications. Given the complexity of plant cell wall, the main challenge is to obtain lignocelluloses with high yield and purity. For a better understanding of lignocellulosic biomass, chromatography stands out as a powerful separation method that can support the lab directed research and pilot scale production of biomaterial and biochemical. This paper provides a review on the characterization of cellulose, hemicellulose and lignin along with their derivatives and decomposed sugar monomers, in particular their isolation and purificationmethods using various specific types of chromatography. Methods with various specific types of chromatography. This review also summarizes different chromatographic methods for obtaining the molecular weights of cellulose, hemicellulose and lignin that have been used in recent years, and highlights future opportunities for the application of those biopolymers.

Fengbo Sun¹ and Qining Sun²*


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Current Status of Two-Dimensional Gel Electrophoresis and Multi-Dimensional Liquid Chromatography as Proteomic Separation Techniques

Proteomics is very important component in the era of post-genomics because it can address functions of genes and some important non-gene-determined biological issues such as Post Translational Modifications (PTMs), splicing, translocation, and spatial structure. Proteome is very complex, including multiple parameters such as kind of proteins, copy number of each protein, PTMs, isoforms, spatial structure of each protein, protein-protein interaction, and protein-other molecule interaction, etc. Moreover, proteome is dynamic, and alters with different conditions such as different physiological processes, different pathological processes, and different disease status.

Xianquan Zhan¹,²,³,⁴*


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Validation of Assay Indicating Method Development of Imatinib in Bulk and Its Capsule Dosage Form by Liquid Chromatography

A novel, simple and economic reverse phase High Performance Liquid Chromatography (RP-HPLC) method has been developed for the quantification of Imatinib in bulk and capsule dosage form with greater precision and accuracy. Separation was achieved on Analytical technologies, C-18, (250mm*4.6mm) column in isocratic mode with mobile phase consisting of acetonitrile: potassium dihydrogen phosphate buffer (pH 2.5) (30:70v/v) with a f low rate of 0.8 mL/min. The detection was carried out at 268 nm. The retention time of Imatinib was found to be 2.67 min. The method was validated as per ICH guidelines. Linearity was established for Imatinib in the range 5-35 μg / ml with r2 value 0.996. The percentage recovery of Imatinib was found to be in the range 99.49-99.67 %. The high recovery and low relative standard deviation confirm the suitability of the proposed method for the estimation of the drug in bulk and capsule dosage forms. Validation studies demonstrated that the proposed RP-HPLC method is simple, specific, rapid, reliable and reproducible for the determination of Imatinib for quality control level.

Nalini Kanta Sahoo¹, Madhusmita Sahu¹, V Alagarsamy¹, B Srividya², and Chinmaya Keshari Sahoo³*