Abstract
This study exclusively focused on the potential application of an inexpensive and sustainable waste macro-algal biomass as an adsorbent for biosorption of copper ions from aqueous medium. After extraction of agar from brown macro-marine algae Gelidiella acerosa, the residual biomass without any further treatment was used as an adsorbent for the expulsion of copper from wastewater. Physicochemical parameters of biosorption like initial pH, initial concentration of Cu(II) solution and biosorbent dosage were optimized using response surface methodology. The maximum copper biosorption potential of 96.36% was observed at optimum conditions of pH of 5.31, initial concentration of 23.87 mg/l and biosorbent dosage of 0.41 g/l. Adopting FTIR and SEM techniques, the surface morphological features of biosorbent were studied. The pseudo-second-order kinetic model was found to be a proper approach to describe biosorption kinetics. All these results confirmed that spent G. acerosa could be considered as an efficient, eco-friendly and economic alternative for Cu(II) removal from aqueous solution.
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Introduction
Enhanced industrial activities with technological innovations and anthropogenic activities with increased population had led to the excessive discharge of heavy metal contaminated wastewater into the aquatic systems. Industrial wastewater infused with heavy metal residues is known to be the most toxic to the aquatic environment and the health of living species (Anantha and Kota 2016). Moreover, heavy metals are non-degradable and accumulate in the environment through the food chain. So, heavy metal-tainted wastewater should be treated before discharging into the aquatic environment.
Among the deleterious heavy metals, copper and its composites are the most common metal pollutants in the environment with the global annual discharge estimated at 939,000 metric tons (Abdolali et al. 2017; Wuana and Okieimen 2011). The most common sources of origin are wastewaters from refineries, metal plating facilities, tanneries, mining operators, etc. (Izquierdo et al. 2010; Calero et al. 2018; Kumar and Chawla 2014). A trace amount of copper is an essential micronutrient for cell functioning. However, excessive intake leads to malfunctioning of liver and brain, mucosal irritation, intestine ulcers, renal system failure and nervous system damage (Kumar and Chawla 2014; Ekere et al. 2016). Persistent copper exposure can also cause Wilson’s disease (Thilagan et al. 2015; Krupanidhi et al. 2008). Hence, meticulous treatment of copper-contaminated water is indispensable before discarding into water systems in order to protect water sources and human health.
Several technologies for the treatment of copper-loaded wastewater have been employed by researchers across the globe. They included precipitation, cementation, membrane separation, oxidation, solvent extraction and ion exchange (Fu and Wang 2011; Dursun 2006). But the majority of these methods are unfit for the treatment when metal concentrations in effluents are less than 100 mg/l (Benaissa and Elouchdi 2007). Moreover, these processes create sludge disposal problems by generating metal-bearing sludge. Over recent years, the removal of copper from wastewater by adsorption attracted the attention of researchers. Studies have been focused on the use of waste or byproducts of various sources such as industries and agriculture as adsorbents, whose use can also eliminate the sludge disposal problem.
Various biological materials have been tested for effective metal recovery from wastewaters which include plant residual biochar, microorganism, activated sludge and micro- and macro-algae (Anastopoulos and Kyzas 2015; Awual 2015; Guang et al. 2012). Among these biomaterials, algae have been reported as most suitable biosorbents due to their abundant availability, high metal-binding affinity, reusability and good surface characteristics (Sari and Tuzen 2008; Babu et al. 2018). Algae’s functionality is mainly attributed to their surface functional groups such as carboxylic, amino and hydroxyl, which binds with metal ions through different interactions like electrostatic forces, ion exchange or complexation (Kiran and Thanasekaran 2011).
Most of the studies were focused on using pure and surface-modified algae as biosorbents for recovery of heavy metals; use of algal waste biomass as biosorbents after extracting valuable products from it was not attempted. In this work, algal biomass after extraction of agar from Gelidiella acerosa (G. acerosa) which is known to be a major source for agar extraction in India was selected as a biosorbent for the expulsion of Cu(II) from aqueous solutions. The objective of the current investigation was to evaluate the feasibility of Cu(II) biosorption by spent G. acerosa and optimize the operational conditions for biosorption of Cu(II) from wastewater. The experimental data are analyzed using different kinetic and equilibrium isotherm models.
Materials and methods
Preparation of spent G. acerosa
Spent waste of marine macro-alga G. acerosa was selected as a biosorbent in the present study. Carmel G. acerosa plants were collected from Gulf of Mannar, Tamil Nadu, India. These algal strains were cleaned many times in tap and double distilled water to remove dirt, salts and external debris; then it was kept dried in open atmosphere for 3 days and further dried in an oven at controlled temperature of 70 °C for another 2 days. Dried G. acerosa, 6 g, was transferred to 500 ml of 1 M NaOH and heated the mixture at 80 °C for 4 h. The algal biomass was separated from the NaOH solution and washed several times with tap water. To extract agar, the algal biomass was taken in 200 ml distilled water and heated at 85 °C for 2 h. The mixture was homogenized in a blender and filtered using filter cloth. After filtration, the biomass was dried at 60 °C for 24 h (Kumar and Fotedar 2009; Villanueva et al. 2010). The dried biomass of algae was chopped into small pieces and ground in domestic grinder. The granulated biomass was sieved through a standard set of sieves and packed in an airtight container.
Reagents and chemicals
A standard copper solution (1000 ppm) was prepared by dissolving 3.91 g of analytical grade CuSO45H2O (Merck India Pvt. Ltd.) in 1000 ml of double distilled water. Working standards of initial Cu(II) concentrations between 20 and 100 ppm were prepared by progressive dilutions of standard copper solution. The initial pH of working standards was normalized using 0.1 M HCl and 0.1 M NaOH
Surface characterization
FTIR spectra of fresh and Cu(II)-treated spent G. acerosa were recorded by following KBr pellet method using Bruker UK (ATR) FTIR spectrophotometer in the spectrum range of 4000–400 cm−1 and presented in Fig. 1. SEM images of fresh and Cu(II)-treated spent G. acerosa were taken using Hitachi S-3700 N SEM (at accelerating voltage 10 kV) and presented in Fig. 2.
Design of experiments
Response surface methodology (RSM) is a multivariable optimization tool used to find the optimal response of a process which is a function of several independent variables through fitting the experimental data to a second-order equation. The three major steps of RSM include design of experimental matrix, development of mathematical model and optimization of response of interest (Chatterjee et al. 2012; Sadhu et al. 2014). To assess the optimum biosorption of Cu(II) (Y) onto spent G. acerosa, three independent variables were followed: initial pH of Cu(II) solution (A), initial Cu(II) concentration in solution (B) and dosage of spent G. acerosa (C). Experiments were designed using face-centered central composite design (FCCCD) of RSM. The ranges and levels (− 1, 0, + 1) of independent variables are presented in Table 1. The second-order polynomial equation relating the independent process variables and the response of interest, i.e., percentage biosorption of Cu(II), is presented in the form of Eq. (1):
where Y is response of system, β0 is constant, \(\beta_{i}\) is linear constant, \(\beta_{ii}\) is quadratic constant and \(X_{i}\) is independent variable.
Experimental procedure
All the experiments designed using FCCCD were performed in batch process. The reaction mixtures of each 30 ml as specified in design matrix were taken in 250-ml conical flasks and stirred in orbital shaker at 180 rpm. All the experiments were conducted up to predetermined equilibrium contact time of 40 min (not discussed here) and holding at ambient temperature. Samples were collected and filtered using Whatman filter paper (No. 1). The metal concentrations of filtrate were measured using atomic absorption spectroscopy (AAS PerkinElmer AAnalyst 400). All experiments were repeated thrice, and statistically analyzed values have been reported. The Cu(II) uptake by spent G. acerosa (mg of copper per g spent G. acerosa) is calculated using Eq. (2):
where \(C_{\text{o}}\) and \(C_{\text{t}}\) are the concentrations of Cu(II) ions (mg/l) before and after equilibrium contact time, V is the volume of Cu(II) aqueous solution taken (ml) and m is the weight of spent G. acerosa (g) added to Cu(II) solution.
Kinetic models
Kinetic modeling of biosorption is very much essential to scale up the process for industrial-scale operations. Moreover, kinetics of a reaction describes the nature of the process, reaction pathways and exact interface resistance for mass transfer. Hence, in the present study fresh experiments were conducted for kinetics analysis with different initial Cu(II) concentrations ranging from 20 to 100 mg/l at optimum pH and temperature of 30 °C, and the data were fitted to various kinetic models such as pseudo-first-order, pseudo-second-order, intra-particle diffusion (Weber and Morris 1964), Boyd (Boyd et al. 1947) and Elovich models (Kellner et al. 2004):
where \(k_{1}\) and \(k_{2}\) are the first- and second-order rate constants, \(q_{\text{e}}\) (mg/g) and \(q_{\text{t}}\) (mg/g) are Cu(II) uptake at equilibrium and time t(min), respectively, \(k_{\text{id}}\) is diffusion constant, C is the constant related to film thickness, F is relative Cu(II) uptake, \(\beta\)t is a mathematical equation, ‘a’ is initial rate of biosorption and ‘b’ is the constant related to activation energy for chemisorption.
Results and discussion
Characterization of spent G. acerosa using FTIR and SEM
Algal cell wall is composed of many functional groups like hydroxyl, carboxyl, amine, sulfate and phosphate, which play a major role in metal binding (Jerold and Sivasubramanian 2016). FTIR is a valuable tool to exploit chemical constituents present on the surface of a material, and it is used to disclose qualitative information regarding the organic compounds (Lammers et al. 2009; Kannan 2014). FTIR spectra of spent G. acerosa before and after biosorption of Cu(II) were recorded at frequencies from 4000 to 400 cm−1 and presented in Fig. 1. Several peaks (Fig. 1a) were observed on the surface of G. acerosa before biosorption, indicating the presence of various functional groups which are responsible for the binding of copper. The medium peak at 3319 cm−1 represents N–H stretching vibration that showed the presence of amine group on the surface of biosorbent. The peaks at 3003 and 2899 cm−1 represent C–H bonds that indicate the presence of carboxylic groups (Jerold and Sivasubramanian 2016; Dulla et al. 2018). In most of the brown algae, 70% of cell wall functional groups are carboxylic and amino groups; these groups play a vital role in metal binding (Meseguer et al. 2016). The peaks at wave numbers of 1730 and 1531 cm−1 are indicative of the presence of S, C=O, NO2 groups (Khan et al. 2016). Strong stretching vibrations in the range of 1250–970 cm−1 are indication of the presence of alcohols and phenols. The peak at 830 cm−1 is associated with the absorbance of O–H group indicating the presence of carboxylic groups. Therefore, it is inferred that the surface of spent G. acerosa comprises functional groups like carboxylic acids, amino, alkenes and alkyl groups.
Comparison of FTIR spectra of spent G. acerosa loaded with copper (Fig. 1b) with that of unloaded revealed significant changes. Formation of new peaks at 1438 and 1248 cm−1 and disappearance of peak at 1724 cm−1 are the clear indications of a possible chemical reaction between copper ions and surface functional groups. Further shifting of peaks in the range of 3500–2800 cm−1 pertaining to carboxylate group reveals the involvement of C–H group in the adsorption of copper ions onto the biosorbent. Moreover, shifting of peak at 830 cm−1 before biosorption to 850 cm−1 after biosorption also discloses the binding of copper ions to amine group present on the surface of spent G. acerosa.
The SEM analysis of spent G. acerosa was carried out to study the surface texture and its modification derived from sorbate interactions, and the result obtained is shown in Fig. 2. It is apparent from the SEM image shown in Fig. 2a that spent G. acerosa has a very rough surface with a good number of pores where there is a good possibility for biosorption of heavy metals ions. A decrease in the number of pores, the presence of shiny particles over the surface and apparent smooth surface after biosorption as shown in Fig. 2b indicate the sorption of copper onto the surface of biosorbent.
Response surface methodology (RSM)
Face-centered central composite design (FCCCD) was used for the optimization of Cu(II) biosorption onto spent G. acerosa by taking input variables as shown in Table 1. A total of 20 experiments designed by FCCCD were conducted, and the obtained results were used for the analysis. Complete design matrix generated using FCCCD with coded variables, response reported from experiments and predicted response for biosorption of Cu(II) onto spent G. acerosa is given in Table 2.
ANOVA for response surface quadratic model
Significance of each individual process variables and overall model significance was studied using analysis of variance (ANOVA), and the results are presented in Table 3. The ANOVA results showed very small “model P value” (< 0.0001) and large “lack of fit P value” (0.989), which discloses the statistical significance of the model. The results also showed that \(R_{\text{adj}}^{2}\) value (0.989) is in good agreement with \(R_{\text{pred}}^{2}\) value (0.999), indicating that there is well-linearized fitness between the experimental values and model-predicted values. Overall, the ANOVA analysis suggests that the model can be used to navigate the design spaces on biosorption of Cu(II). The probable P values of each individual factors and their interactive terms suggest that A, B, C, AB and A2 were significant model terms. Though the individual parameter effects namely pH, initial concentration and biosorbent dosage were significant, combined effect of pH and initial concentration was more significant. Square effect of pH has also shown moderate significance on biosorption. Similar results were reported by Liu et al. (2018) for biosorption of copper using rape straw powder.
The mathematical equation of relationship between the response of system and independent input variables in terms of coded factors is:
From the above equation, it could be observed that factors A and C had a positive effect, i.e., proportional effect, while factor B had a negative effect, i.e., inverse effect on biosorption of copper.
Optimization and substantiation of biosorption
To estimate the maximum Cu(II) removal by spent G. acerosa and optimum processing conditions, optimization tool of RSM was used and predicted solution was shown in contour plot (Fig. 3). The maximum Cu(II) removal predicted is 96.362% at optimum process conditions of pH of 5.31, initial Cu(II) concentration of 23.87 mg/l and G. acerosa dosage of 0.41 mg/l. The validity of optimization process was examined by conducting a fresh experiment at the above-predicted values and reported 94.25% Cu(II) removal, which was in the vicinity of RSM predicted value. Hence, the predicted values of independent variables at maximum Cu(II) removal were considered as optimum process conditions for biosorption of Cu(II) onto spent G. acerosa.
Analysis of interactive effects of two variables
Response surface plots were used to investigate the interaction effects of any two variables on biosorption. Figure 4a shows the interactive effect of metal ions concentration and pH of the solution on biosorption of Cu(II). In contrast to a decrease in biosorption with an increase in concentration, a moderate increase was noticed with an increase in initial concentration, which clearly manifests the impact of pH over initial concentration on metal removal. Three-dimensional plot of effect of pH and biosorbent dosage on biosorption of Cu(II) is shown in Fig. 4b. It clearly shows the effect of pH over effect of biosorbent dosage. It could be observed that at higher biosorbent dosage, the % biosorption of Cu(II) was high, and a possible reason for this is that the increase in binding sites with dosage and the increase in negative charge on surface of biosorbent with pH together must have contributed for an increase in biosorption of Cu(II). The interactive effects of the biosorbent dosage and initial metal ions concentration can be inferred from the response plot (Fig. 4c), holding pH at central values. From Fig. 4c, it could be observed that there are no significant inferences. Since dosage and initial concentration have no significant effect on biosorption, the interaction effect of these two variables was also found to be insignificant. As shown in Table 3 of ANOVA, the P value of the factor BC is very high, which also confirms the insignificance effect of that factor.
Kinetic studies
Kinetic modeling is fundamental in order to determine the affinity or capacity of the sorbent which in turn governs the residence time in the design of biosorption process. The fitness of kinetic data to pseudo-first- and second-order rate equations is described in Fig. 5, and corresponding rate constants, predicted copper uptake and R2 values are reported in Table 4. Though the regression coefficient values of first-order model are in the range of 0.99–0.98, the predicted metal uptakes are not in good agreement with the experimental values. Hence, pseudo-first-order rate equation is not appropriate for determining kinetics. In the case of pseudo-second order, high correlation coefficients and very closely predicted and experimental metal uptake values show the significance of the model for representing kinetics of biosorption of copper. Therefore, biosorption of copper onto spent G. acerosa follows pseudo-second-order model with chemisorption as a rate-limiting step. Further kinetic data were fitted to the Elovich model to investigate the biosorption mechanism, and the results are plotted in Fig. 5. The plots are linear with good correlation coefficients (R2 in the range of 0.985), indicating that the kinetic data follow the Elovich model. The intra-pore diffusion of copper ions is investigated by fitting the kinetic data to intra-particle diffusion model. Figure 6a shows that the kinetic data are not well correlated with the intra-particle diffusion model and also plots are not passing through origin. Hence, the same data are fitted to the Boyd model to find out exact rate-limiting step. Bt values were calculated from the data and then plotted against contact time, as shown in Fig. 6b. It is clear that the plots are linear but not passing through the origin.
Good kinetic properties are very much essential for good adsorbents, i.e., they must be capable of transferring adsorbing molecules rapidly to adsorption sites. The kinetic parameters of this experiment are similar to the biosorption of kinetics of Cu(II) by other biosorbents derived from algal species like Halimeda gracilis (Jayakumar et al. 2015), Euglena gracilis (Winters et al. 2017) and Arthrospira platensis (Markou et al. 2015). The fitness of data to second-order model suggests that biosorption of Cu(II) onto the spent G. acerosa was controlled by chemisorptions and probably took place through surface exchange reactions until the surface active sites are fully occupied by metal ions. Moreover, fitness of data to the Elovich model reiterates the above-mentioned argument that the biosorption of copper follows chemisorptions. Fitness of kinetic data to intra-particle diffusion model (Fig. 6a) reveals that the linear plots are not passing through the origin which indicates that the biosorption of Cu(II) onto spent G. acerosa is controlled by external pore diffusion. Further investigation by fitting the data to Boyd model (Fig. 6b) with high correlation coefficient (R2 = 0.998) confirms that the film resistance is the rate-controlling step. Many researchers reported the similar results on biosorption of Cu(II) using other adsorbents (Kumar and Chawla 2014; Ofomaja et al. 2010; Yahaya et al. 2009).
Conclusions
In conclusion, the results of the present investigation indicate that biosorbent prepared from spent marine macro-algae G. acerosa, after extraction of agar, seems an efficient, most economic and eco-friendly adsorbent for biosorption of Cu(II) present in industrial wastewater. FTIR and SEM analysis established the presence of various functional groups on biosorbent surface and biosorption of Cu(II) ions onto G. acerosa. FCCCD of RSM was used to optimize the process conditions and maximize the Cu(II) removal. ANOVA showed a correlation coefficient (R2 = 0.99) significant P value, thus ensuring significant adjustment of quadratic model with experimental values. Biosorption kinetics followed pseudo-second-order model with film resistance as rate-controlling mechanism. The findings of the present investigation indicated that spent G. acerosa can be successfully used for biosorption of Cu(II) from aqueous and industrial wastewater.
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Acknowledgements
We would like to thank the entire team of Center of Excellence for Advanced Materials, Manufacturing, Processing and Characterization (CoExAMMPC) of Vignan’s Foundation for Science and Technology, Guntur, and Advanced Analytical Laboratory of Andhra University, Visakhapatnam, for their support in entire instrumental analysis.
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Dulla, J.B., Tamana, M.R., Boddu, S. et al. Biosorption of copper(II) onto spent biomass of Gelidiella acerosa (brown marine algae): optimization and kinetic studies. Appl Water Sci 10, 56 (2020). https://doi.org/10.1007/s13201-019-1125-3
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DOI: https://doi.org/10.1007/s13201-019-1125-3