International Scholarly Research Notices

International Scholarly Research Notices / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 968402 | 10 pages | https://doi.org/10.1155/2014/968402

Recovery of Ga(III) by Raw and Alkali Treated Citrus limetta Peels

Academic Editor: Shaobin Wang
Received05 Mar 2014
Accepted04 Jun 2014
Published24 Jul 2014

Abstract

Alkali treated Citrus limetta peels were used for recovery of Ga(III) from its aqueous solution. The raw and alkali treated peels were characterized for functional groups. The efficiency of adsorption increased from 47.62 mg/g for raw peels to 83.33 mg/g for alkali treated peels. Between pH 1 and 3, the adsorption increased and thereafter decreased drastically. The adsorption followed pseudosecond order kinetics and Langmuir isotherm gave the best fit for the experimental data. Desorption studies showed 95.28% desorption after 3 cycles for raw peels while it was 89.51% for alkali treated peels. Simulated Bayer liquor showed 39.57% adsorption for gallium ions on raw peels which was enhanced to 41.13% for alkali treated peels.

1. Introduction

Gallium is the 30th in terms of abundance at an average concentration of 19 mg/g. It finds significant applications in the semiconductor industry through use of gallium arsenide and gallium nitride. Gallium is classified as a “strategic” metal, since it is used in high-tech gadgets like microwave transceivers, DVDs, laser diodes in CDs, and so forth and defence-related activities [13]. Gallium nitrate and gallium citrate are used in medical imaging as radio contrast agents [4]. Gallium arsenide is used to make rectifiers and amplifiers. Due to good adhesion to glass and high reflectivity, gallium is used in high quality mirrors [5]. There are no gallium-containing minerals of any economic significance. Due to its uniform distribution in soil, its extraction is uneconomical. It is usually associated with aluminium in bauxite, nephelines, and other ores and recovered as a by-product while producing alumina. The United States Geological Survey has estimated total world’s primary gallium production to be about 273 tonnes in 2012 [6], the estimated consumption being 280 tonnes. As per the report of Roskill Information Services, neomaterial estimated that 50% of gallium consumed worldwide in 2010 came from recycled sources [7]. As per working Group Report of 12th Five Year Plan, India produced around 55 kg of gallium in recent years. Two plants, namely, Hindalco Industries Ltd. at Renukoot and National Aluminium Co. Ltd., at Damanjodi Alumina Refinery, Odisha, recover gallium [8]. It is derived from wastes of industrial processes, such as flue dusts from the zinc industry, waste generated during smelting of phosphate to produce elemental phosphorus, or sludge from the aluminium industry. Since aluminium lies in the same group of periodic table, gallium has affinity towards it. Bauxite (the primary aluminium ore) typically contains 0.003 to 0.01% gallium. Concentrations in zinc ores (e.g., sphalerite) are comparable. Since primary sources are scarce, the general strategy is to recover gallium from intermediate industrial products.

Bayer liquor is one of the important resource for recovery of gallium. About 90% of the world’s primary gallium is produced from Bayer liquor [9]. In the Bayer process, about 70% of the gallium content of bauxite is leached along with aluminium and about 30% is retained in the red mud. Gallium accumulates in the Bayer liquor in successive cycles, attaining concentrations of 100–200 mg/L [10]. Gallium is also obtained from the iron mud or residues that result from the purification of zinc sulphate solutions, in zinc production. There are four kinds of recovery methods for gallium, namely, fractional precipitation, electrochemical deposition, solvent extraction, and ion exchange. Fractional precipitation is a complex process; solvent extraction is efficient but very slow; electrochemical method uses mercury cathode which is banned due to mercury toxicity, whereas ion exchange gives effective recovery of gallium. Industrial resins such as Duolite ES-346 and PHG586 may be used; however, the process is very expensive. Hence, further research for cheap, efficient, and environmentally friendly recovery of gallium is essential [11].

Biosorption studies have mainly focused on the removal and recovery of heavy metal ions from industrial effluents, detoxification being their primary goal. Functional groups present in the biosorbents that are responsible for metal binding are carboxyl, phosphoryl, sulfhydryl, amino, sulfate, imidazole, thioether, phenol, amide, and hydroxyl in various biomolecules of peptide, protein, and polysaccharide moieties of the cell walls. These functional groups bind the metal ions mainly by adsorption, ion exchange, and chelating effects [12].

Very few reports have been published on the removal/recovery of gallium using natural adsorbent [1315]. Citrus limetta peels are a natural pectinacious agrowaste material, typically generated in large quantities by the fruit juice industry, rich in pectin with abundant presence of carboxyl groups. It is reported that these peels have a metal binding mechanism similar to brown algal biosorbents since pectin is chemically similar to the brown algal cell wall polysaccharide alginate [6, 7]. These peels have been found to be very good adsorbents for Pb(II) and Cd(II) [1618]. Our previous studies have shown good binding capacity by citrus peels for Pb(II) ions [18].

In the present work, the adsorption of Ga(III) from the aqueous solution of gallium nitrate and from the simulated Bayer liquor on Citrus limetta peels, in its raw as well as alkali treated form, has been reported.

2. Materials and Methods

2.1. Materials

Citrus limetta fruit peels procured from local juice shop were used as biosorbents. Demineralized water was used throughout the experiment for dilution and washing purposes. Stock solution of 1000 mg/L was prepared from gallium nitrate salt (Sigma-Aldrich, India). Gallium standard used for calibration of Atomic Absorption Spectrometer (Model: GBC 932plus, Austria) was supplied by Merck Inc., Germany.

pH adjustment of metal ion solution was achieved by appropriate addition of 0.1 M NaOH and 0.1 M HCl.

2.2. Methods
2.2.1. Preparation of Biosorbent

Citrus limetta peels procured from local juice shop were soaked in water for 4 h, washed, and cleaned using 1% nonionic detergent solution and again with demineralised water. The washed peels were dried at 60°C till constant weight, reduced to small particle size using a grinder, sieved to mesh sizes between 425 and 800 μ, and stored in zip lock bags. The biomass thus obtained was termed as raw citrus peels (RCP).

2.2.2. Modification of Functional Groups on RCP

The raw peels were treated with different chemical agents as reported to enhance their adsorption capacity. This data is further presented in Table 1 [19].


ModificationMetal uptake (mg/L)

Nil (RCP)24.40
1 M malonic acid treated peels24.31
1 M oxalic acid treated peels21.67
20% H2O2 treated peels30.78
0.1 M sodium hydroxide treated peels (ACP)34.59
1 M citric acid treated peels23.90
1 M succinic acid treated peels27.05
Acetylated peels27.08
Chlorosulphonic acid treated peels23.00
Methane sulphonic acid treated peels23.33
0.1 M potassium dichromate treated peels27.12

RCP was treated with 0.05 M aqueous NaOH for 3 h at room temperature. It was then washed thoroughly with demineralized water till neutral pH and then dried in an oven at 60°C for 24 h and stored in zip lock bags to avoid contamination with moisture. It was termed as alkali treated citrus peels (ACP). The weight loss of biomass due to alkali treatment was estimated experimentally.

2.2.3. Estimation of Gallium Ions

Ga(III) concentration in aqueous solution was determined by Atomic Absorption Spectrometer (GBC 932 plus, Australia) at 287.1 nm with an air-acetylene flame. Each time, AAS was calibrated by using standard 1000 mg/L Ga(III) solution.

2.2.4. ATR-IR Spectroscopy

The functional groups present on the surface of RCP and ACP were determined by recording the infrared spectra of these peels using Shimadzu 8400S FT-IR spectrometer (Figure 2).

2.2.5. Scanning Electron Microscopy (SEM)

Microscopic images of RCP and ACP were taken by scanning electron microscope (Jeol JSM 6380 LA spectrometer, Tokyo, Japan) to reveal the morphological aspects of the surface of the biomass samples.

2.2.6. Estimation of Acidic Groups

Number of acidic sites present on RCP and ACP were estimated by methylene blue absorption method [20, 21]. When a biomass is treated with a cationic dye like methylene blue, the coloured cations of the dye are quantitatively absorbed by acidic groups present on the material forming strong ionic linkage. A weighed sample of the biomass was added to an Erlenmeyer flask containing 25 mL of aqueous methylene blue chloride solution (300 mg/L) and 25 mL borate buffer of pH 8.5. It was kept for 3 h at 25°C and then 5 mL of filtered sample was transferred to a volumetric flask containing 10 mL 0.1 M HCl followed by dilution to 100 mL. The decrease in the intensity of colour was measured on UV-visible spectrometer (Techcomp; UV-VIS 8500) at the = 650 nm. Using the calibration plot, the amount of unabsorbed methylene blue was calculated. The value gives quantitative information about the acidic sites present on the surface of peels.

2.2.7. Batch Wise Adsorption Experiments

Unless otherwise stated, for all the batch wise adsorption experiments, 100 mg of dry adsorbent was placed in 40 mL Ga(III) solution having varying initial concentrations ranging from 40 mg/L to 200 mg/L at pH 3.0 in a 250 mL stoppered Erlenmeyer flask and agitated in an orbital shaker (Rossari Biotech Ltd., Mumbai) at 150 rpm for 4 h at room temperature. The biomass was then allowed to settle down and the supernatant solution was pipetted out. The solutions were estimated for the remaining Ga(III) concentration using flame type AAS.

The biosorption capacity of gallium per unit of dry biomass (mg of Ga/g of dry biomass) was calculated by using where is the equilibrium adsorption capacity (mg/g), and are the initial and equilibrium concentrations of Ga(III) (mg/L), respectively, is the volume of adsorbate (L), and is the mass of adsorbent (g).

The biosorption efficiency, %, of the metal ion was calculated from The optimum pH for the biosorption was evaluated by adjusting the pH between 1 and 3 with an interval of 0.5 using 1 M HCl.

The kinetics of adsorption of Ga(III) was studied by shaking 2.5 g of adsorbent samples with 200 mL of approximately 100 mg/L solutions of Ga(III) at pH 3.0 and at room temperature (30°C) up to 300 min in a 250 mL Erlenmeyer flask at 150 rpm. At each predetermined time, 1 mL of the solution was removed and tested for its metal content using flame type AAS. The amount of metal ions adsorbed was evaluated from the difference between the initial and final concentrations of Ga(III) ions in the solution.

2.2.8. Isotherm Modeling

Out of many isotherm models, the Langmuir and Freundlich models are the most commonly studied due to their ease of interpretation [22]. Langmuir isotherm was initially derived for adsorption of gases on solid surfaces (Figure 6), and it considered sorption as a chemical phenomenon; the sorbent surface contains only one type of binding site and the sorption is limited to monolayer [23]. It is given by where is the metal uptake, is the maximum biosorption capacity, is the constant related to adsorption energy, and is the equilibrium concentration of metal ions. The Langmuir parameters can be determined from the slope and the intercept of the plot versus , based on the linearized form of the above equation, can be written as Freundlich proposed an empirical isotherm relation as expressed in in which and are Freundlich constants (Figure 7). As the Freundlich isotherm is exponential, it can be reasonably applied only in the low to intermediate concentration range [24]. The equation can be linearized as Besides these two common adsorption isotherms, Sips isotherm is also widely used to study the biosorption mechanism of pectin containing compounds [25] (Figure 8). This isotherm is a combination of Langmuir and Freundlich isotherm equations, deduced for predicting the heterogeneous adsorption systems and to overcome the limitation of the rising adsorbate concentration associated with Freundlich isotherm model. At low adsorbate concentrations, it reduces to Freundlich isotherm; while, at high concentrations, it predicts a monolayer adsorption capacity characteristic of the Langmuir isotherm (Tables 4 and 5). As a general rule, the equation parameters are governed mainly by the operating conditions such as the alteration of pH, temperature, and concentration. Sips isotherm can be expressed as in which is the Sips constant [26] (Table 6).

2.2.9. Kinetic Modeling

Biosorption data under nonequilibrium conditions is usually described by pseudofirst order and pseudosecond order equations [27].

Pseudofirst Order Equation. The pseudofirst order kinetic equation or Lagergren equation is given as in which is the amount of adsorbate adsorbed at time , is the value at equilibrium, and is the constant [28].

Pseudosecond Order Equation. The pseudosecond order kinetic equation has been frequently employed to analyze the biosorption data using different adsorbates and biosorbents as reviewed by Ho and McKay [29]. Consider in which is a constant.

2.2.10. Adsorption-Desorption Cycles

Repetitive adsorption-desorption studies were carried out to evaluate the economic feasibility of the process. Desorption of Ga(III) from previously adsorbed peels was carried out by shaking them with 40 mL of desorbing media at 30°C for 240 min. Different desorbing media with varied concentrations, studied for the desorption, were HCl, HNO3, and H2SO4. The metal ion content in the desorbing media was then estimated using AAS.

2.2.11. Regeneration of Biosorbent

RCP and ACP were thoroughly washed with demineralized water after desorption, treated with 40 mL of 0.025 M NaOH solution for 240 min, washed again, dried at 60°C in hot air oven for 24 h, and reused for another adsorption-desorption cycle.

2.2.12. Preparation of Simulated Bayer Liquor

The process feasibility was checked by adsorbing the Ga(III) ions from the simulated spent Bayer liquor on RCP and ACP. It was prepared in laboratory by adding the components which are generally present in spent Bayer liquor in their stoichiometric amount [30]. Thus, 25 g of Na2CO3 were dissolved in hot water and cooled to room temperature. To this, 125 g of NaOH pellets were added slowly with stirring followed by addition of 120 g of Al(OH)3. The solution was heated near to boiling point, cooled, filtered, and diluted to 1 L. Then 14.7 mL of gallium stock solution (13.62 g/L) was transferred into the solution and the solution was made up to 1 L by adding water. Forty mL of this simulated spent Bayer liquor was taken in an Erlenmeyer flask, with pH adjusted to 3.0 by 0.1 M HCl, and subjected to adsorption on 0.1 g of biomass. The concentration of Ga(III) ions before and after the adsorption was estimated on AAS. Weight loss of the biomaterials during adsorption process was also estimated gravimetrically.

3. Results and Discussion

3.1. Effect of Pretreatment on Ga(III) Biosorption

Citrus peels are mainly made up of pectin (around 30% by mass), which is rich in galacturonic acid [31]. In nature, around 80% of carboxyl groups of galacturonic acid are present in esterified form as methyl carboxylate. The nonesterified galacturonic acid units can be either free acids (carboxyl groups) or salts with sodium, potassium, or calcium. The salts of partially esterified pectins are called pectinates. Salts below 5% degree of esterification are called pectates and the insoluble acid form is the pectic acid [32]. Alkali treatment is very effective in hydrolysis of these esterified galacturonic acid units and converts them into free acid sites. It also ruptures the cell wall and exposes more functional groups, thereby promoting the heavy metal adsorption by preferential ion-exchange mechanism [33]. Earlier oxidative pretreatment of cellulosic biomass such as jute and coir with hydrogen peroxide has shown to enhance the adsorption capacity for Pb(II) cations [34, 35]. Oxidized coir also showed enhanced adsorption of gallium (19.42 mg/g) compared to unmodified coir (13.75 mg/g) [13].

Raw Citrus limetta peels (RCP), a pectin containing waste biomaterial, have shown good potential to adsorb Pb(II) ions [18]. Initial experiments on RCP also showed the potential to adsorb Ga(III) ions from its aqueous solution ( = 21.70 mg/g for = 70 mg/L). RCP was given various chemical treatments that are reported to enhance the adsorption capacity of biomaterials [19] (Table 1).

Among those, it was found that the alkali treatment was the most efficient in enhancing the adsorption capacity of peels and hence the concentration of NaOH was optimized at RT (30°C) and 2 h treatment time (Figure 1) (Table 2). Different acidic groups such as carboxylic and sulphonic acid also get converted into their sodium forms which have been shown to promote heavy-metal ion adsorption [36].


NaOH concentration (N)Weight loss (%)

0.00000.0
0.00119.0
0.01019.2
0.05019.6
0.10020.8

3.2. FT-IR Spectra of Biomass

FTIR spectra of peels showed peak at ~3350 cm−1 which is characteristic of hydroxyl group, mainly due to water. The peak observed at ~1625 cm−1 is attributed to asymmetric stretching of the carboxylic (C=O) double bond. The peaks observed at 2924 cm−1 and 2856 cm−1 in ACP are due to asymmetric and symmetric stretching modes of methylene groups. No strong shift in the wave number ~1750 cm−1 was observed in RCP, although the intensity of peak increased in ACP which is characteristic of carbonyl group of carboxylic acid (–COOH) and ester (–COOR). This indicates increase in the number of carboxylic groups in ACP which has also been quantified by methylene blue absorption method to 6.32 10−2 mmol/g from 5.40 10−2 mmol/g in RCP. Thus, the alkali treatment caused modification of the ester functional groups to carboxylic acid groups present in raw peels.

3.3. Scanning Electron Microscopy

SEM images clearly indicate the morphological changes in the peels on alkali treatment. It can be easily depicted from the SEM that the surface of peels is highly heterogeneous. As seen in Figure 3, ACP surface shows more cavities and more number of opened up pores as compared to RCP indicating that it has increased the surface area available for adsorption. Alkali treatment proved to be effective in rupturing the cell walls due to which more functional groups are exposed on the surface and became available for adsorption. Apart from that, no further significant morphological changes were apparent in the SEM images.

3.4. Estimation of Acidic Groups on the Surface of Peels

The carboxyl groups present in the biosorbents have been proved to be directly responsible for the sorption of heavy metals [17, 18]. These are the most abundant acidic functional groups and the adsorption capacity of peels is directly related to the presence of these sites in pectin in the form of galacturonic acid. Estimation of acidic groups on the surface of peels available for sorption reveals that ACP contains contains more carboxylic acid groups (6.32 10−2 mmol/g) as compared to RCP (5.40 10−2 mmol/g). This has been attributed to the alkaline hydrolysis of some of the ester groups present on the surface of the peels under the treatment conditions. Structure of pectin before and after hydrolysis is as shown in Figure 4.

3.5. Effect of Initial Solution pH

pH is one of the most crucial factors which drives the efficiency of adsorption, as it governs the speciation of the metal ions in aqueous solution and also determines the degree of protonation on the biomass. At lower pH, protons compete with the metal ions thereby decreasing the adsorption, while, at higher pH, metal ions form corresponding hydroxides get precipitated out.

The biosorption of Ga(III) was strongly affected by initial solution pH. The sorption capacity of RCP has increased from 16.29 mg/g at pH 1.0 to 35.59 mg/g Ga(III) at pH 3.0 (Figure 5) indicating an increase in adsorption capacity. Beyond pH 3.0, precipitation occurs, as gallium forms a hydroxide gel and loses its solution characteristics [36]. In case of ACP, the increase in adsorption capacity registered was from 18.23 mg/g to 44.44 mg/g at similar pH values.

In aqueous solution, gallium is always present in its hydrated form with six molecules of water held strongly to make an octahedral complex. The strength of metal-oxygen bond weakens O–H bond; hence, hydrolysis occurs and protons are released, thus giving acidic solution. The more metal ion concentration in the solution is, the more the hydrolysis is and, hence, the more acidic the solution becomes [37, 38]. Ga(III) ions are Lewis acids, and, in aqueous solution, they form aqua ions of the formula . The aqua ions undergo hydrolysis; the hydrated gallium ions have six molecules of water which are held firmly giving an octahedral complex. The first hydrolysis step is given generically as

Thus, the aqua cations behave as acids in terms of Brønsted-Lowry acid-base theory. This effect is easily explained by considering the inductive effect of the positively charged metal ion, which weakens the O–H bond of an attached water molecule, causing the liberation of a proton relatively easy to make the solution acidic.

Like other metal ions, the adsorption of Ga(III) is also highly influenced by pH [3941]. At lower pH, the affinity towards the proton of the binding site of peels is much greater than that of the metal ion (H+ ≫ M3+), compared with that at higher pH where M3+ ≫ H+ [36]. Therefore, the adsorption is less at a lower pH of 1.0 which remains almost unaffected till pH 1.5 as Ga(III) has strong competition with protons and then it increases with the pH as the concentration of protons decreases till pH 2.5 is attained.

From the data given in Table 3, it is clear that the adsorption of Ga(III) on Citrus limetta peels is much higher than any other biosorbent used in earlier studies [13]. This may be attributed to enhanced carboxylic acid sites in ACP pectin.


Biosorbent usedInitial Ga concentration (mg/L) (mg/g)Reference

Oxidized coir20319.42[13]
Alkali treated peels20076.26This study


AdsorbentLangmuir isothermFreundlich isotherm
(mg/g) RMSE RMSE

RCP47.620.0310.993.023.841.610.997.08
ACP83.330.0220.993.693.691.900.987.72


AdsorbentLangmuir isotherm Freundlich isotherms
(mg/g)

RCP46.540.0334.040.50
ACP76.260.0244.110.60


AdsorbentSips isotherm

RCP1.1241.2120.0180.99
ACP2.4120.7870.0380.99

3.6. Adsorption Isotherm

The adsorption data were fitted to Langmuir and Freundlich adsorption isotherms. The metal loading capacities of RCP and ACP as calculated from the slope of the plot versus were found to be 47.62 and 83.33 mg/g, respectively. Though the data seems to be fitting equally well with the Langmuir and Freundlich isotherms, RMSE error value for Langmuir plot is much lower than Freundlich plot. This suggests that the Langmuir model gives better fit for both the adsorbents. “” and “” were calculated from the intercept and slope of the plot log  versus log . Freundlich isotherm values of “” were 1.61 and 1.90 for RCP and ACP, respectively, suggesting favourable adsorption by ACP.

3.7. Kinetic Modelling

Pseudosecond order plot shows better fit than pseudofirst order for RCP and ACP. Figure 9 represent the linearized plots for second order model for RCP and ACP. Higher value of initial rate, , in ACP (2.50 mg/gmin) suggests favorable adsorption. The values for pseudosecond order model has been listed in Table 7. The kinetic study reveals closeness of the predicted and experimental values, which are 25.00 and 24.11 for RCP and 32.26 and 29.77 for ACP, respectively. Pseudosecond order plot gives best fit for RCP as well as ACP; hence, it was considered that adsorption of Ga(III) on RCP and ACP takes place via pseudosecond order kinetics.


AdsorbentExperimental (mg/g)
( /min)

(mg/g)
Initial rate,
(mg/g·min)

RCP24.112.725.000.991.69
ACP32.262.429.770.992.50

3.8. Desorption Studies

Desorption efficiency of the adsorbent is crucial to the recovery of gallium. The metal ion loaded adsorbent was most effectively desorbed by using 0.5 M HCl, when different acids (HCl, H2SO4, and HNO3) with different concentrations (0.1 M–1.0 M) were tried. Ga(III), adsorbed on the surface of the adsorbent, exchanges with the H+ ion of the acid due to its high affinity towards the functional groups, behaving as a cation exchanger. Desorption in the first cycle was observed to be more than 95%, which decreased marginally in the subsequent cycles. The weight loss study of the adsorbents during the adsorption-desorption cycles indicated that, after the first complete cycle, the weight loss for RCP was 19.19% while that for ACP was 17.53%. It increased to 37.05% for RCP and to 55.45% for ACP after the second cycle. Even after the third cycle, the same adsorbent can be used by seeing its good adsorption capacity.

3.9. Regeneration Studies

Although the Citrus limetta peels is a waste material obtained from the orange fruit, any chemical treatment to convert it into a better adsorbent adds to the cost. In order to make the process economically viable, the peels after desorption of Ga(III) were regenerated using 0.025N NaOH and reused for another adsorption-regeneration cycle. Low concentration of alkali is used as regeneration media for economic viability. Regeneration of the peels was studied for 3 cycles and showed comparative adsorption in the next cycles.

3.10. Simulated Bayer Liquor Sample Analysis

Synthetic Bayer liquor sample was analyzed for the efficiency of biosorbent for adsorption-desorption cycles (Table 9). It was observed that RCP showed 39.57% adsorption of gallium from the simulated spent Bayer liquor while ACP showed 41.13% adsorption. Both the adsorbents showed nearly complete desorption in 0.5 M HCl as desorbing media. The weight loss of biomass after first cycle was observed to be 29.98% for RCP and 18.03% for ACP. The decrease in the adsorption capacity as compared to pure aqueous solution of gallium may be attributed to the presence of other metal ions such as Na(I) and Al(III) present in the solution. These results are presented in Table 8. It may be seen that RCP and ACP are competitive to synthetic ion exchange resin showing adsorption capacities of 7.32 and 7.61 mg/g, respectively, which are higher than that of reported value (6.0 mg/g) on resin with hydroxamic acid ligand [3].


AdsorbentCycle 1Cycle 2Cycle 3
% adsorption% desorption% weight loss% adsorption% desorption% weight lossOverall weight loss% adsorption% desorption% weight lossOverall weight loss

RCP58.9898.7119.1934.3795.7716.2139.4037.0895.264.7640.16
ACP68.5195.3717.5356.0089.7812.9030.4355.4689.512.8833.31


AdsorbentAdsorption (%)Desorption (%) Weight loss (%)

RCP39.5798.3529.98
ACP41.1392.2318.03

4. Conclusion

Waste biomass Citrus limetta peels were effectively used to adsorb gallium ions from aqueous solution. When treated with sodium hydroxide, the alkali treated peels (ACP) showed enhanced metal removal capacity. Optimum pH for adsorption was found to be 3.0. Kinetic data showed that the equilibrium reached within 180 minutes. Pseudosecond order model proved to be the best fit whereas isotherm studies reveal that the metal ion adsorption capacity of 47.62 mg/g for RCP was enhanced to 83.33 mg/g for ACP. The adsorbents showed good stability up to three adsorption-desorption cycles and hence proved practical to use at scale up level. Also RCP and ACP showed significant adsorption in synthetic Bayer liquor sample which highlights the use of Citrus limetta peels at commercial level.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgment

The author Sachin C. Gondhalekar gratefully acknowledges the funding by the University Grants Commission’s fellowship under Special Assistance Programme.

References

  1. R. R. Moskalyk, “Gallium: the backbone of the electronics industry,” Minerals Engineering, vol. 16, no. 10, pp. 921–929, 2003. View at: Publisher Site | Google Scholar
  2. I. R. Grant, “Gallium arsenide from mine to microcircuit,” Transactions of the Institution of Mining and Metallurgy, C: Mineral Processing and Extractive Metallurgy, vol. 97, pp. 48–52, 1987. View at: Google Scholar
  3. P. Selvi, M. Ramasami, M. H. P. Samuel, P. Adaikkalam, and G. N. Srinivasan, “Recovery of gallium from Bayer liquor using chelating resins in fixed-bed columns,” Industrial and Engineering Chemistry Research, vol. 43, no. 9, pp. 2216–2221, 2004. View at: Google Scholar
  4. G. Iosilevsky, D. Front, L. Bettman, R. Hardoff, and Y. Ben-Arieh, “Uptake of gallium-67 citrate and [2-3H]deoxyglucose in the tumor model, following chemotherapy and radiotherapy,” Journal of Nuclear Medicine, vol. 26, no. 3, pp. 278–282, 1985. View at: Google Scholar
  5. E. F. Borra, R. Content, L. Girard, S. Szapiel, L. M. Tremblay, and E. Boily, “Liquid mirrors: optical shop tests and contributions to the technology,” Astrophysical Journal Letters, vol. 393, no. 2, pp. 829–847, 1992. View at: Google Scholar
  6. U.S. Geological Survey, Mineral Commodity Summaries, 2013.
  7. A 2011 Roskill Report, “Gallium: global industry markets & outlook,” Roskill Report, 2011. View at: Google Scholar
  8. Govt of India, Ministry of Mines, Indian Beauro of Mines, Indian Mineral Year Book, vol. 2, 2011.
  9. X. Lu, L. Wang, X. Wang, and X. Niuesearch, “Research progress in gallium recovery technology,” Nonferrous Metals, vol. 60, pp. 105–108, 2008. View at: Google Scholar
  10. A. M. G. Figueiredo, W. Avristcher, E. A. Masini, S. C. Diniz, and A. Abrão, “Determination of lanthanides (La, Ce, Nd, Sm) and other elements in metallic gallium by instrumental neutron activation analysis,” Journal of Alloys and Compounds, vol. 344, no. 1-2, pp. 36–39, 2002. View at: Publisher Site | Google Scholar
  11. Z. Zhao, Y. Yang, Y. Xiao, and Y. Fan, “Recovery of gallium from Bayer liquor: a review,” Hydrometallurgy, vol. 125-126, pp. 115–124, 2012. View at: Publisher Site | Google Scholar
  12. J. Wang and C. Chen, “Biosorbents for heavy metals removal and their future,” Biotechnology Advances, vol. 27, no. 2, pp. 195–226, 2009. View at: Publisher Site | Google Scholar
  13. U. S. Suryavanshi and S. R. Shukla, “Adsorption of Ga(III) on oxidized coir,” Industrial and Engineering Chemistry Research, vol. 48, no. 2, pp. 870–876, 2009. View at: Publisher Site | Google Scholar
  14. H. Eroglu, S. Yapici, C. Nuhoglu, and E. Varoglu, “Biosorption of Ga-67 radionuclides from aqueous solutions onto waste pomace of an olive oil factory,” Journal of Hazardous Materials, vol. 172, no. 2-3, pp. 729–738, 2009. View at: Publisher Site | Google Scholar
  15. H. Eroglu, S. Yapici, and E. Varoglu, “An investigation of the biosorption of radioactive gallium-67 in an aqueous solution using rose residue,” Journal of Chemical and Engineering Data, vol. 55, no. 8, pp. 2848–2856, 2010. View at: Publisher Site | Google Scholar
  16. S. Schiewer and A. Balaria, “Biosorption of Pb2+ by original and protonated citrus peels: equilibrium, kinetics, and mechanism,” Chemical Engineering Journal, vol. 146, no. 2, pp. 211–219, 2009. View at: Publisher Site | Google Scholar
  17. E. Njikam and S. Schiewer, “Optimization and kinetic modeling of cadmium desorption from citrus peels: a process for biosorbent regeneration,” Journal of Hazardous Materials, vol. 213-214, pp. 242–248, 2012. View at: Publisher Site | Google Scholar
  18. U. Suryavanshi and S. R. Shukla, “Adsorption of Pb2+ by Alkali-treated citrus limetta peels,” Industrial and Engineering Chemistry Research, vol. 49, no. 22, pp. 11682–11688, 2010. View at: Publisher Site | Google Scholar
  19. S. Srivastava and P. Goyal, Novel Biomaterials: Decontamination of Toxic Metals from Wastewater, Springer, 2010.
  20. G. Sèbe, P. Pardon, F. Pichavant, S. Grelier, and B. De Jéso, “An investigation into the use of eelgrass (Zostera noltii) for removal of cupric ions from dilute aqueous solutions,” Separation and Purification Technology, vol. 38, no. 2, pp. 121–127, 2004. View at: Publisher Site | Google Scholar
  21. D. Klemm, B. Philipp, T. Heinze, U. Heinze, and W. Wagenknecht, “Fundamentals and analytical methods,” in Comprehensive Cellulose Chemistry, vol. 1, p. 236, John Wiley & Sons, Weinheim, Germany, 1998. View at: Google Scholar
  22. K. Y. Foo and B. H. Hameed, “Insights into the modeling of adsorption isotherm systems,” Chemical Engineering Journal, vol. 156, no. 1, pp. 2–10, 2010. View at: Publisher Site | Google Scholar
  23. I. Langmuir, “The adsorption of gases on plane surfaces of glass, mica and platinum,” The Journal of the American Chemical Society, vol. 40, no. 9, pp. 1361–1403, 1918. View at: Google Scholar
  24. A. Z. Freundlich, “Über die adsorption in lösungen,” Zeitschrift fur Physikalische Chemie, vol. 57, pp. 385–470, 1906. View at: Google Scholar
  25. K. V. Kumar and K. Porkodi, “Relation between some two- and three-parameter isotherm models for the sorption of methylene blue onto lemon peel,” Journal of Hazardous Materials, vol. 138, no. 3, pp. 633–635, 2006. View at: Publisher Site | Google Scholar
  26. R. Sips, “Combined form of langmuir and freundlich equations,” Journal of Chemical Physics, vol. 16, pp. 490–495, 1948. View at: Google Scholar
  27. Y. Liu and Y.-J. Liu, “Biosorption isotherms, kinetics and thermodynamics,” Separation and Purification Technology, vol. 61, no. 3, pp. 229–242, 2008. View at: Publisher Site | Google Scholar
  28. S. Lagergren, “Zur theorie der sogenannten adsorption gelöster stoffe. Kungliga Svenska Vetenskapsakademiens,” Handlingar, vol. 24, no. 4, pp. 1–39, 1898. View at: Google Scholar
  29. Y. S. Ho and G. McKay, “Pseudo-second order model for sorption processes,” Process Biochemistry, vol. 34, no. 5, pp. 451–465, 1999. View at: Publisher Site | Google Scholar
  30. F.-F. Zha, A. G. Fane, and C. J. D. Fell, “Liquid membrane processes for gallium recovery from alkaline solutions,” Industrial and Engineering Chemistry Research, vol. 34, no. 5, pp. 1799–1809, 1995. View at: Google Scholar
  31. C. D. May, “Industrial pectins: sources, production and applications,” Carbohydrate Polymers, vol. 12, no. 1, pp. 79–99, 1990. View at: Google Scholar
  32. P. Sriamornsak, “Chemistry of pectin and its pharmaceutical uses: a review,” Journal of Pharmacy and Pharmaceutical Sciences, vol. 44, pp. 207–228, 1998. View at: Google Scholar
  33. S. R. Shukla, R. S. Pai, and A. D. Shendarkar, “Adsorption of Ni(II), Zn(II) and Fe(II) on modified coir fibres,” Separation and Purification Technology, vol. 47, no. 3, pp. 141–147, 2006. View at: Publisher Site | Google Scholar
  34. S. R. Shukla and R. S. Pai, “Comparison of Pb(II) uptake by coir and dye loaded coir fibres in a fixed bed column,” Journal of Hazardous Materials, vol. 125, no. 1–3, pp. 147–153, 2005. View at: Publisher Site | Google Scholar
  35. S. R. Shukla and R. S. Pai, “Adsorption of Cu(II), Ni(II) and Zn(II) on modified jute fibres,” Bioresource Technology, vol. 96, no. 13, pp. 1430–1438, 2005. View at: Publisher Site | Google Scholar
  36. P. Persson, K. Zivkovic, and S. Sjöberg, “Quantitative adsorption and local structures of gallium(III) at the water-α-FeOOH interface,” Langmuir, vol. 22, no. 5, pp. 2096–2104, 2006. View at: Publisher Site | Google Scholar
  37. J. Burgess, Metal Ions in Solution, Ellis Horwood, New York, NY, USA, 1978.
  38. D. T. Richens, The Chemistry of Aqua Ions: Synthesis, Structure, and Reactivity: A Tour Through the Periodic Table of the Elements, John Wiley & Sons, 1997.
  39. N. Fiola, I. Villaescusaa, M. Martínezb, N. Mirallesb, J. Pochc, and J. Serarols, “Sorption of Pb(II), Ni(II), Cu(II), and Cd(II) from aqueous solution by olive stone waste,” Separation and Purification Technology, vol. 50, no. 1, pp. 132–140, 2006. View at: Google Scholar
  40. R. H. S. F. Vieira and B. Volesky, “Biosorption: a solution to pollution?” International Microbiology, vol. 3, no. 1, pp. 17–24, 2000. View at: Google Scholar
  41. B. Volesky, Biosorption of Heavy Metals, vol. 3, CRC Press, Boca Raton, Fla, USA, 1990.

Copyright © 2014 Sachin C. Gondhalekar and Sanjeev R. Shukla. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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