Citric acid (CA) was evaluated in terms of its efficiency as a biodegradable chelating agent, in removing zinc (Zn) from heavily contaminated soil, using a soil washing process. To determine preliminary ranges of variables in the washing process, single factor experiments were carried out with different CA concentrations, pH levels and washing times. Optimization of batch washing conditions followed using a response surface methodology (RSM) based central composite design (CCD) approach. CCD predicted values and experimental results showed strong agreement, with an R2 value of 0.966. Maximum removal of 92.8% occurred with a CA concentration of 167.6 mM, pH of 4.43, and washing time of 30 min as optimal variable values. A leaching column experiment followed, to examine the efficiency of the optimum conditions established by the CCD model. A comparison of two soil washing techniques indicated that the removal efficiency rate of the column experiment (85.8%) closely matching that of the batch experiment (92.8%). The methodology supporting the research experimentation for optimizing Zn removal may be useful in the design of protocols for practical engineering soil decontamination applications
Soil contamination by heavy metals has become a global concern, due to the threat to ecosystems and human health of their high toxicity levels1,2. In agricultural areas, heavy metal contamination, even if not associated with specific health hazards, may reduce economic output2. The United States Environmental Protection Agency (USEPA) has classified Zinc (Zn) as a harmful heavy metal, and placed it on the list of priority pollutants3.
Soils polluted with heavy metals can be decontaminated through a variety of methods of remediation, such as stabilization, solidification, electroremediation and phytoremediation4. Among the techniques of remediation, the simplicity of chemical soil washing, its low cost, short duration and high efficiency, makes it a practical option for metal removal5,6,7. The selection of a viable solution is a fundamental determinant of the level of efficiency of extraction in the washing process3,6,8. Environmental factors, and the cost and availability of the extraction solution, are other important considerations in selecting a washing reagent3. Due to its superior capacity to complex with a number of heavy metal ions, the chelating agent ethylenediaminetetra acetic acid (EDTA) has frequently been used in polluted soil treatments9. However, EDTA usage has been restricted due to its poor level of biodegradability8 and it has been replaced by natural biodegradable chelants, citric acid (CA) being the most prominent10,11, due to its minimal impact on the physical and chemical properties of soil12.
Optimum soil washing conditions are prerequisite, particularly in the case of scaled up applications, to minimise costs and maximise Zn removal efficiency. Classical optimization, in which only one factor is changed at a time in order to measure its effect, is time consuming and requires many experiments. In practice, it overlooks, or disregards, the interactive effects between individual components. Response surface methodology (RSM), in which effective parameters are optimised simultaneously, overcomes the deficiencies of single factor optimization13,14. Using RSM substantially reduces the number of experiments necessary to predict the conditions for best performance15,16. Furthermore, modelling of the process refines the interpretation of complex phenomena and provides a basis for process scaling17.
Regarding the advantages of RSM, it has been used successfully in the modelling and optimization of soil washing conditions, for the efficient removal of Zn from severely contaminated soil. Thus, our principal research objective set out to investigate the process of removing Zn from highly contaminated soil, using CA as an ecologically benign, biodegradable chelant in a batch washing process. In order to predict optimal conditions for Zn removal, we developed a quadratic polynomial model, using a central composite design (CCD) based on RSM. Thereafter, the optimized batch washing conditions were applied to a column washing experiment, to compare the efficiency of the two washing methods.
Materials and Methods
A contaminated soil sample was collected from the topsoil layer (0–20 cm) around the Angouran zinc mine in Zanjan Province, Iran (Lat. 47°15′17″, Long 35°44′37″). The sample was air dried, homogenized, sifted through a 2 mm nylon mesh sieve for the removal of larger particles, and stored at room temperature in plastic containers.
The following properties of the sample soil were analysed: texture, pH, electrical conductivity (EC), cation exchange capacity (CEC), soil organic matter (SOM) and calcium carbonate equivalent (CCE). To determine texture, the hydrometer method as described by Gee et al.18 was used. SOM was determined by dichromate oxidation, and soil pH and electrical conductivity (EC) were determined in a soil-solution ratio of 1:5 using pH and electrical conductivity meter19. CEC was measured by saturating soil with 1 M NH4OAc at pH 7, and CCE was determined by the acid neutralization method19. The total zinc content was measured using a flame atomic absorption spectrophotometer (Shimadzu AA-7000) based on a soil sample with HNO3-HCl-HClO4 mixture at a 1:2:2 ratio (v/v/v). Values of these sample physicochemical properties are listed in Table 1.
The sample was calcareous (CCE = 21%), slightly alkali (pH = 7.8), with texture classified as clay loam. The total Zn concentration of 5657 mg.kg−1 surpassed the level permitted in soil used primarily for the agricultural production of food crops.
Preliminary soil washing experiments
The preliminary ranges of washing variables, the CA concentration, pH of solution and washing time were determined in a sequence of single factor experiments, using a soil-solution ratio of 1:10 (w/v) in 100 mL acid-rinsed polycarbonate plastic bottles. For each run, 5 grams of the contaminated sample was added to 50 mL of the washing reagent.
To investigate the effect of CA concentration on Zn removal, a range of concentrations of CA from 5 to 400 mM were tested. The pH test was based on 200 mM CA at a range of pH values from 2.0–10.0, altered with diluted HNO3 and/or NaOH solution. A 200 mM CA solution was also prepared to measure the effects of washing time, ranging from 15 to 300 min, on removal efficiency.
The suspensions in each test were mixed using a mechanical shaker, running at a constant 150 rpm for the predefined time. Following the shaking, suspensions were centrifuged for 10 min, at 4000 rpm, and then filtered through a Whatman (0.45 µm) filter membrane. The supernatant Zn concentration was measured using a flame atomic absorption spectrophotometer (AAS). All of these tests were conducted in duplicate.
Experimental design and optimization
The RSM based central composite design (CCD) with independent variables was followed to create the optimum synergy of and to check the response patterns. The specific parameters whose ranges had been established in the preliminary testing, CA concentration (20–200 mM), pH (4–8), and washing time (30–150 min) were thus optimized (Table 2).
For the CCD, the selected experimental points included eight cubic points, six axial points (α = ±1.68), and six replicates at the centre point (α = 0).
Optimum variable values were calculated from the experimental response and coded at five levels from −1.68, −1, 0, +1, and +1.68 as defined by Eq. (1).
where, xi denotes the coded value of variable Xi, X0 the actual value of Xi at the centre point, and ΔXi the increment.
CCD model was designed to fit the second order polynomial model, using a multiple regression program according to Eq. (2).
where Y represents the variable of response (percentage Zn removal), Xi and Xj independent coded variables, and β0, βi, βii, βij the intercept term, linear, quadratic and interaction effects, respectively16,20. Random error (ɛ) expresses the measure of difference between observed and predicted values. To give greater insight into the CCD results, Pareto analysis was used to calculate the percentage effect of each independent variable (Pi) on the removal of Zn21 (Eq. 3):
Minitab 14 statistical package (MINITAB Inc., PA, USA) was used for the statistical analysis of the results.
Results and Discussion
Preliminary washing experiment
In the preliminary testing, CA removal efficiency followed the trend of decreasing Zn removal with increasing pH (Fig. 1a). Results indicated that when pH was decreased from 8 to 4, Zn removal increased considerably from 5.5% to 61.3%, while remaining almost constant for lower pH values. This implies that acidic conditions, rather than alkaline, are preferable for Zn removal. Previous research findings have indicated that the pH of the solution plays a major role in the removal efficiency of heavy metals from contaminated soils6,8,22. Accordingly, the behaviour of metal-chelant complexes, solubility of the zinc hydroxides, competition between H+ and the Zn2+ for sorption sites on soil particles, as well as the surface charge of the soil colloids, is directly controlled by pH. A rise in pH of the CA solution increases the cationic heavy metal adsorption on the soil surface, inner sphere complexion, and may also increase the probability of precipitation reactions 6,23.
Figure 1(b) illustrates the effect of CA concentration on Zn removal efficiency, at a fixed washing time of 120 minutes. The zinc removal was less than 0.5% when distilled water was applied as a washing solution, which might be due to the very low solubility of zinc compounds in the water. Further, the zinc removal increased considerably for concentrations of CA up to 100 mM, with a slower increase at higher concentrations, which can be ascribed to the high efficiency of CA as a chelating agent. Citric acid forms a square planar complex with heavy metals, through binding to the citrate anions with cations. Huang et al.24 also noted the increase in heavy metals removal with increasing CA concentrations, in the range lower than the 200 mM. This could be explained by the high stability content (Log KML = 6.1) for Zn-CA complexes25.
Washing time is another influential factor in remediation of heavy metals from contaminated soil, in that the process of desorption is a kinetic equilibrium. Figure 1c shows the kinetics of Zn removal by CA (concentration = 100 mM; pH = 4.0) for washing times ranging from 15 to 300 min. Zn removal efficiency increased within the time range of 30 to 120 min, before approaching a relatively constant level, indicating that soil washing with CA is a time dependent process. This observation shows a strong agreement with other studies, regarding washing time6,7,22,26. The initial rapid increases in Zn removal, followed by a levelling, may be due to the fact that the chelation process reaches equilibrium at a certain length of washing time.
From the preliminary results, the range of independent variables, as listed in section 2.3 (Table 1), was selected for the RSM based central composite design (CCD). In the following section, the results of Zn removal optimization, using RSM based CCD are presented.
The CCD experiment design for Zn removal, based on three independent factors with a five- level structure, is shown in Table 3. The broad range of Zn removal (from 5.35 to 79.11%) demonstrates the necessity to optimize washing conditions. The quadratic polynomial equation (Eq. 4), obtained from experimental results which expressed as coded units, defines the relationship between the independent variables (CA concentration, pH, and washing time) and response (percentage Zn removal).
The CCD predicted Zn removal values, as determined by the quadratic polynomial model (Eq. 4), are shown in Table 3, and display generally strong agreement with the measured values of Zn removal derived from the experiment results. The model validation resulted in a coefficient of determination (R2) of 0.966, and root mean square error (RMSE) of 4.4% (see supporting information, Fig. S1) in agreement of empirical and predicted values. Thus, 3.4% of the variation in Zn removal is not supported by the CCD model.
Analysis of variance (ANOVA)
Table 4 displays the ANOVA results for the fitting of the quadratic model. The table indicates that in both the linear and square parameters, the effects of the prominent variables are significant on response, with p-values < 0.05. Similarly, the response levels of the interactions of independent variables are also significant with p-values < 0.05.
In the ANOVA Table, the model F-value of 31.66 is notably greater than the tabulated F-distribution value of 3.02 at 95% significance, indicating that the model is conclusively efficient in predicting experimental results. Table 5 lists the regression coefficients, t-values, and p-values for the linear, quadratic, and effects of variable interactions, at a significance level of 95%. The significance of each term of the model was verified by means of the associated p-value.
The liner effect of pH, CA concentration and the second order effect of pH are significant model terms on Zn removal (p-value < 0.05). Furthermore, interaction effects of all three independent variables (pH, CA concentration, and washing time) are also significant.
Pareto analysis ranks the effect of variables on response (Eq. 3). The analysis indicated that the order of effective variables on Zn removal was pH (66.52%) > CA concentration (15.45%) > pH and CA concentration interaction (6.37%) > washing time and CA concentration interaction (3.83%)> washing time and pH interaction (3.62%) > quadratic effect of pH (2.88%). These six terms accounted for 98.67% of cumulative effects on Zn removal (Fig. 2).
To produce the optimised model for Zn removal, the final quadratic response surface model (Eq. 5), expressed as coded units, represents the CCD model with the removal of insignificant terms (p-value > 0.05).
Effect of independent variables
The independent variable interactions are illustrated by 3D surface plots, derived from the quadratic polynomial model, in Fig. 3(a–c). In each 3D surface plot, two variables are altered, while the third variable is maintained at a constant value of zero coded level. The shape of these plots supports an interpretation of the level and quality of the interactions of the independent variables.
Figure 3b shows the trend of Zn removal against upon coinciding variation of washing time and CA concentration at constant pH of 6. As expected, the removal efficiency increased proportionate to the CA concentration. Removal was significantly enhanced as the washing time increased from 30 to 150 min. An increased CA concentration promotes the reaction of the heavy metal ion-ligand complex to move toward the direction of chelate formation6,7. Similarly, Ren et al.5 reported a significant increase in the efficiency of Zn removal from sewage sludge, with increases of the CA concentration over the range of 200–1000 mM.
The combined effect of CA concentration level and pH value on Zn removal efficiency, at a fixed washing time of 90 min, is presented in Fig. 3b. Here it can be seen that the efficiency of Zn removal depends strongly on CA concentration and pH, with a higher CA concentration increasing efficiency, but a higher pH having a negative effect. The pH effect was more notable at higher CA concentrations, and thus maximum Zn removal occurred at lower pH values, with increased CA concentration. As the pH decreases, the surface of the soil colloids commonly acquires a positive charge, due to the protonation of functional groups. This promotes heavy metals desorption from the soil surface. Additionally, hydrogen ions are weak competitive cations which can replace the adsorbed heavy metals via the cation exchange mechanism27.
The effect of simultaneous variations of pH and time is illustrated in Fig. 3c. The CCD model was applied with pH increasing from 4 to 8, and washing time from 30 to 150 min. Figure 3c illustrates that removal efficiency is enhanced by decreasing the pH, but the effect of time appears to be more intricate. According to the results of the CCD model (Table 4), Zn removal is not directly influenced by washing time, the effect of which is only significant in terms of interactions. Likewise, Tejowulan and Hendershot28 demonstrated that the heavy metal removal rate was dependent on chelant concentration, and not on washing time.
Determination of optimal conditions
Optimal values of the independent variables, CA concentration, pH and washing time, as given in Table 6, to achieve a Zn removal efficiency of 95%, were obtained by a response optimizer. For validation, a confirmation experiment was conducted, with four replicates at the optimum conditions predicted by CCD model. Zn removal efficiency obtained from the experiments at optimal condition (92.80 ± 4.84%) showed a strong agreement with that of the predictive model value (95%). The results suggest that the use of CCD for optimization of soil washing conditions, to attain the maximum efficiency of Zn removal, has proven successful.
Leaching column experiment
To compare the efficiency of batch and column washing techniques, a leaching column experiment was executed at the optimum CCD batch washing values of CA concentration (167.6 mM) and pH (4.43). The leaching column consisted of PVC tube (20 cm length, 5 cm diameter), with the contaminated soil sample positioned at a height of 10 cm by uniform tapping with a wooden rod to create a constant bulk density of 1.3 g.cm−3 (total porosity ≈ 50%). The top and bottom of the column were filled with an approximately 1 cm filter gravel layer. Wathman NO. 47 filter paper was used to preclude the loss of soil particles, from the bottom of the each column, during leaching.
The cumulative leaching of the Zn is depicted as a function of pore volume in Fig. S2 (see supporting information). The leaching column experiment indicated that Zn removal by CA solution (167.6 mM, pH = 4.43) is a two-step process, commencing with a fast desorption within the initial pore volumes, followed by a slower desorption occurring over the subsequent pore volumes. The more pore volumes that are added, the more Zn may be removed. From the first 15 pore volumes, equal to a 1:6 (w/v) soil to water ratio, 76.24% of the final total Zn was leached from the soil. Thereafter, the removal efficiency increased slightly, culminating in 85.8% at the 26th pore volume (soil water ratio of 1:10 (w/v) similar to the batch experiments). Further soil washing had little effect on the overall Zn removal, which is consistent with the findings of Lo et al.29 and Elmaslar-Özbaş and Balkaya30, in regard to leaching.
The comparison of two soil washing techniques with CA, batch washing vs. column washing, indicated that the removal efficiency for the column experiment (85.8%) is comparable with those of the batch experiment (92.8%). It is noteworthy that although Zn removal by batch washing experiment is less time consuming, and slightly more efficient than column washing, the latter technique has some benefits. Column leaching minimizes worker exposure to contamination. Additionally, it is more practical and has the potential for the economical treatment of relatively large amounts of soil. During the column washing procedure the soil structure remains undisturbed, unlike the batch techniques4. However, it should be noted that the column leaching technique may be very difficult to apply in low permeable soils31.
Zn removal from contaminated soil, by CA as a biodegradable chelant, was modelled and optimized by the response surface methodology (RSM) based central composite design (CCD). The following conclusions can be drawn from this research:
RSM based CCD is a promising tool (R2 = 96.6%) for modelling and optimizing Zn removal from contaminated soil by CA.
The optimum values of pH, CA concentration, and process time were estimated at 4.43, 167.6 mM, and 30 min, respectively, with 95% Zn removal as target efficiency.
It was found that the pH and CA concentration with a percentage importance of 66.52% and 15.45% respectively, are the most significant parameters in the Zn removal process.
The optimal values for pH and CA concentration from the batch washing experiments could be successfully translated to column washing, and the removal yields were efficient and comparable under both techniques.
Niinae, M., Nishigaki, K. & Aoki, K. Removal of lead from contaminated soils with chelating agents. Materials transactions 49(10), 2377–2382 (2008).
Race, M. et al. Copper and zinc removal from contaminated soils through soil washing process using ethylenediaminedisuccinic acid as a chelating agent: A modeling investigation. Journal of Environmental Chemical Engineering 4, 2878–2891 (2016).
Moon, D. H., Lee, J. R., Wazne, M. & Park, J. H. Assessment of soil washing for Zn contaminated soils using various washing solutions. Journal of Industrial and Engineering Chemistry 18(2), 822–825 (2012).
Yang, Z. et al. Remediation of heavy metal contamination in calcareous soil by washing with reagents: A column washing. Procedia Environmental Sciences 16, 778–785 (2012).
Ren, X. et al. Citric acid and ethylene diamine tetra-acetic acid as effective washing agents to treat sewage sludge for agricultural reuse. Waste Management 46, 440–448 (2015).
Wang, G. et al. Application of response surface methodology for the optimization of lead removal from contaminated soil using chelants. RSC Advances 5(71), 58010–58018 (2015).
Wang, J. et al. Removal of Pb and Zn from contaminated soil by different washing methods: the influence of reagents and ultrasound. Environmental Science and Pollution Research 22(24), 20084–20091 (2015).
Wang, G. et al. Efficiency of nanoscale zero-valent iron on the enhanced low molecular weight organic acid removal Pb from contaminated soil. Chemosphere 117, 617–624 (2014).
Chen, C., Chen, Y., Xie, T., Wang, M. K. & Wang, G. Removal, redistribution, and potential risks of soil Cd, Pb, and Zn after washing with various extractants. Environmental Science and Pollution Research 22(21), 16881–16888 (2015).
Wuana, R. A., Okieimen, F. E. & Imborvungu, J. A. Removal of heavy metals from a contaminated soil using organic chelating acids. International Journal of Environmental Science & Technology 7(3), 485–496 (2010).
Ding, Y. Z., Song, Z. G., Feng, R. W. & Guo, J. K. Interaction of organic acids and pH on multi-heavy metal extraction from alkaline and acid mine soils. International Journal of Environmental Science and Technology 11(1), 33–42 (2014).
Li, G., Yang, X., Liang, L. & Guo, S. Evaluation of the potential redistribution of chromium fractionation in contaminated soil by citric acid/sodium citrate washing. Arabian Journal of Chemistry. 10, 539–545 (2017).
Aghaeinejad-Meybodi, A., Ebadi, A., Shafiei, S., Khataee, A. & Rostampour, M. Degradation of antidepressant drug fluoxetine in aqueous media by ozone/H2O2 system: process optimization using central composite design. Environmental technology 36(12), 1477–1488 (2015).
Kakelar, M. M. & Ebrahimi, S. Up-scaling application of microbial carbonate precipitation: optimization of urease production using response surface methodology and injection modification. International Journal of Environmental Science and Technology 13, 2619–2628 (2016).
Jentzer, J. B., Alignan, M., Vaca-Garcia, C., Rigal, L. & Vilarem, G. Response surface methodology to optimise Accelerated Solvent Extraction of steviol glycosides from Stevia rebaudiana Bertoni leaves. Food chemistry 166, 561–567 (2015).
Kumar, N. M., Ramasamy, R. & Manonmani, H. K. Production and optimization of L-asparaginase from Cladosporium sp. using agricultural residues in solid state fermentation. Industrial Crops and Products 43, 150–158 (2013).
Alkhatib, M. F., Mamun, A. A. & Akbar, I. Application of response surface methodology (RSM) for optimization of color removal from POME by granular activated carbon. International Journal of Environmental Science and Technology 12(4), 1295–1302 (2015).
Gee G. W. & Bauder J. W. Particle-size analysis. In: Methods of soil analysis. Part 1, Klute, A. (Ed.), SSSA, Madison; WI, 383–411 (1986).
Rowell D. Soil science: methods and applications, Department of Soil Science, University of Reading. Prentice-Hall, Englewood Cliffs, ISBN 0-582-08784-8 (1994).
Maddipati, P., Atiyeh, H. K., Bellmer, D. D. & Huhnke, R. L. Ethanol production from syngas by Clostridium strain P11 using corn steep liquor as a nutrient replacement to yeast extract. Bioresource technology 102(11), 6494–6501 (2011).
Mousavi, S. M., Niaei, A., Salari, D., Panahi, P. N. & Samandari, M. Modelling and optimization of Mn/activate carbon nanocatalysts for NO reduction: comparison of RSM and ANN techniques. Environmental technology 34(11), 1377–1384 (2013).
Zou, Z. et al. The study of operating variables in soil washing with EDTA. Environmental Pollution 157(1), 229–236 (2009).
Appel, C. & Ma, L. Concentration, pH, and surface charge effects on cadmium and lead sorption in three tropical soils. Journal of Environmental Quality 31(2), 581–589 (2002).
Huang, K., Inoue, K., Harada, H., Kawakita, H. & Ohto, K. Leaching of heavy metals by citric acid from fly ash generated in municipal waste incineration plants. Journal of Material Cycles and Waste Management 13(2), 118–126 (2011).
Polettini, A., Pomi, R. & Calcagnoli, G. Assisted washing for heavy metal and metalloid removal from contaminated dredged materials. Water, air, and soil pollution 196(1-4), 183–198 (2009).
Wu, Q., Cui, Y., Li, Q. & Sun, J. Effective removal of heavy metals from industrial sludge with the aid of a biodegradable chelating ligand GLDA. Journal of hazardous materials 283, 748–754 (2015).
Zhang, T. et al. Chelant extraction of heavy metals from contaminated soils using new selective EDTA derivatives. Journal of hazardous materials 262, 464–471 (2013).
Tejowulan, R. S. & Hendershot, W. H. Removal of trace metals from contaminated soils using EDTA incorporating resin trapping techniques. Environmental Pollution 103(1), 135–142 (1998).
Lo, I. M., Tsang, D. C., Yip, T. C., Wang, F. & Zhang, W. Significance of metal exchange in EDDS-flushing column experiments. Chemosphere 83(1), 7–13 (2011).
Elmaslar-Özbaş, E. & Balkaya, N. Extraction of heavy metals from compost using a mixture of Na2EDTA and Na2S2O5: column studies. Journal of soil science and plant nutrition 12(3), 525–534 (2012).
Heil, D. M., Samani, Z., Hanson, A. T. & Rudd, B. Remediation of lead contaminated soil by EDTA. I. Batch and column studies. Water, Air, & Soil Pollution 113(1), 77–95 (1999).
The authors are indebted to the Department of Soil Science (Urmia University) for providing laboratory facilities.
The authors declare no competing interests.
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Asadzadeh, F., Maleki-Kaklar, M., Soiltanalinejad, N. et al. Central Composite Design Optimization of Zinc Removal from Contaminated Soil, Using Citric Acid as Biodegradable Chelant. Sci Rep 8, 2633 (2018). https://doi.org/10.1038/s41598-018-20942-9
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