Thermodynamics and Mechanism of the Adsorption of Heavy Metal Ions on Keratin Biomasses for Wastewater Detoxification

Olawale, Salaudeen Abdulwasiu; Bonilla-Petriciolet, Adrián; Mendoza-Castillo, Didilia Ileana; Okafor, Chibueze Charles; Sellaoui, Lotfi; Badawi, Michael

doi:https://doi.org/10.1155/2022/7384924

Adsorption Science & Technology

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Abstract Introduction Results and Discussion Conclusions Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

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Sustainable Valorization of Biowaste for Environmental Remediation

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Research Article | Open Access

Volume 2022 | Article ID 7384924 | https://doi.org/10.1155/2022/7384924

Thermodynamics and Mechanism of the Adsorption of Heavy Metal Ions on Keratin Biomasses for Wastewater Detoxification

Salaudeen Abdulwasiu Olawale,¹Adrián Bonilla-Petriciolet,²Didilia Ileana Mendoza-Castillo,^2,3Chibueze Charles Okafor,⁴Lotfi Sellaoui,⁵and Michael Badawi⁶

Academic Editor: Silvano Mignardi

Received28 Sept 2021

Revised07 Feb 2022

Accepted22 Feb 2022

Published19 Mar 2022

Abstract

The analysis of thermodynamics and mechanism of the adsorption of cadmium, chromium, copper, and lead ions from aqueous solution with two keratin-based biomaterials, namely, human hair and sheep fur, is reported in this paper. The effect of initial ion concentration, temperature, pH, contact time, and biomaterial amount on the removal of these heavy metal ions using these keratinous adsorbents was studied. The adsorption of heavy metal ions was highly dependent on the operating parameters where pH and temperature showed the highest impact. Maximum adsorption capacities of these biomaterials were up to 1.33 and 1.40 mmol/g for chromium ions using human hair and sheep fur, respectively. Adsorption kinetic rates of tested heavy metal ions were calculated via a pseudo-second-order model, and they ranged from 0.054 to 0.261 g/mmol·min. A detailed thermodynamic analysis of lead ion adsorption was performed showing an endothermic removal of this adsorbate with both human hair and sheep fur with adsorption enthalpies of 84.5 and 97.1 kJ/mol, respectively. Statistical physics calculations demonstrated that this heavy metal ion was adsorbed via a multi-interaction mechanism especially for human hair. These keratinous biomaterials showed competitive adsorption capacities especially for chromium ion removal and can outperform commercial activated carbons and other adsorbents reported in literature.

1. Introduction

The earth is made up of about 70% water with only about 3% being freshwater mostly found as polar ice and underground aquifers. The surface freshwater in rivers, lakes, and other reservoirs is estimated less than 0.25% of the total available amount worldwide [1]. In the last decades, the rapid industrialization in metallurgy, power plants, oil processing, mining, paints, and other important industrial sectors has generated an increment of the discharges of harmful heavy metals into the water bodies [2]. Natural sources (e.g., weathering of rocks and minerals, volcanic activities, and soil erosion) also contribute to the heavy metal pollution. Several studies have confirmed that heavy metals are toxic to different life forms (e.g., plants, aquatic organisms, and humans) and can generate a significant environmental impact. Mercury, copper, arsenic, chromium, cadmium, and lead are examples of toxic heavy metals in the context of environmental protection [3]. These metals are nonbiodegradable and toxic if a chronic exposure occurs even at low concentrations and can persist in nature thus causing their bioaccumulation via food and/or drinking water [4–6]. For instance, copper and zinc are required by humans at low dose, but they are toxic at concentrations higher than 1 mg/L, as stated by the World Health Organization [7–10].

The detoxification of wastewaters polluted by heavy metals is fundamental to protect the environment and public health [11], and consequently, it is a current research topic [12]. Different treatment technologies have been applied to face the pollution caused by heavy metals such as coagulation and flocculation [13, 14], ion exchange [15, 16], advanced oxidation [17–19], membrane filtration [20–23], electrochemical degradation [24–26], and biodegradation. These techniques could imply economical and/or technical disadvantages including low removal effectiveness at high metal concentrations, colateral generation of toxic residues, high sensitivity to operating conditions, long processing time, application of expensive chemicals and supplies, high energy consumption, and capital investment [27]. Different studies have been performed to overcome these deficiencies and to achieve an effective reduction of the concentration of these pollutants in treated effluents.

Adsorption is a cost-effective method to detoxify fluids polluted by heavy metals [28, 29]. This separation process implies the transfer of adsorbate (i.e., pollutant) from the fluid (i.e., water or industrial effluent) to the surface of a solid matrix (i.e., adsorbent) that should have a tailored surface chemistry and porosity to reach an effective separation. It also offers the possibility to recover the adsorbate(s) loaded on the adsorbent surface via desorption thus facilitating the adsorbent recycling [30]. The effectiveness of adsorption of heavy metal ions is affected by several operating variables like contact time, adsorbent amount, temperature, initial metal concentration, and pH [31]. Also, textural parameters and surface functionalities of the material used as an adsorbent are paramount to achieve a successful removal of these pollutants. Therefore, it is important to characterize, assess, and model the performance of low-cost materials as adsorbents for the removal of heavy metal ions at different operating conditions with the aim of identifying the best alternatives for real-life and industrial applications.

In particular, a large number of low-cost adsorbents have been studied and, in less extent, some of them have been commercialized for removing heavy metal ions from water [32]. These adsorbents can be obtained from mineral, organic, or biological sources [33]. Keratinous materials from biological origin like human hair (HH), sheep fur (SF), and chicken feathers can be employed as alternative adsorbents of these pollutants in their native forms or after an activation procedure that implies their surface functionalization. These biomaterials can be effective in the removal of heavy metal ions due to their high stability, water insolubility, intricate networks, and surface rich in functional groups like hydroxyl, carboxyl, amino, and sulphur [34]. Therefore, the utilization and valorization of biomaterials are an alternative to reduce the operational costs of wastewater treatment and to develop effective and sustainable adsorption processes.

In this manuscript, the study of mechanism and thermodynamics of the adsorption of copper (Cu²⁺), chromium (Cr⁶⁺), cadmium (Cd²⁺), and lead (Pb²⁺) ions on HH and SF is reported. These biomaterials have been studied in their native form to analyze and characterize the adsorption properties of these ions and to calculate kinetic and thermodynamic parameters that allowed the interpretation and understanding of the corresponding adsorption mechanisms. These findings are the main contribution and novelty of this paper. As stated, these biomaterials are low-cost and renewable and offer the possibility to be used as raw adsorbents and feedstock to prepare composites and new materials for the removal of water pollutants. Finally, statistical physics calculations were also performed to interpret and explain the adsorption mechanism of these heavy metal ions using these keratin-based biomaterials where Pb²⁺ ion was utilized as a representative adsorbate of this type of relevant inorganic pollutants.

2. Methodology

2.1. Description of Keratin-Based Biomaterials and Their Characterization

HH and SF were the keratin-containing biomaterials utilized as adsorbents. The HH sample was washed with deionized water and detergent and dried at 298 K. The experimental tests of adsorption of heavy metal ions were done with a HH sample . SF was collected from a Fulani settlement in Kwali Area Council of the Federal Capital Territory Abuja FCT, and these samples were handled in the same way as the case of HH.

Specific moisture content, ignition mass loss, pH, and bulk density were quantified for these biomaterials using standard procedures [4]. Functional groups of the surfaces of both HH and SF were analyzed via FTIR at room temperature, and results were used to identify their role for the removal of heavy metal ions. Absorption spectra were recorded at 4000–400 cm^-1 wavenumber with 4 cm^-1 resolution and 45 scans using a Shimadzu FTIR-8400S equipment. SEM micrographs of both HH and SF were recorded before and after the adsorption at different magnifications to analyze their surface morphology with a JEOL JSM 6100 equipment.

2.2. Adsorption Experiments

The adsorption of heavy metal ions on HH and SF was assessed at different conditions of pH (1–5), adsorbent dosage (0.2-4 g/L), initial metal ion concentration (mmol/L), and contact time (10–360 min) at 298 K. Equilibrium studies were also performed at 293–323 K and pH 4 to analyze the adsorption thermodynamics. All removal tests were done with batch adsorbers properly stirred at 270 rpm. Double-distilled water and analytical grade reagents were utilized to prepare all the required solutions, while pH adjustment was done with HNO₃ (0.1 M) and NaOH (0.1 M). The concentrations of Cu²⁺, Cr⁶⁺, Cd²⁺, and Pb²⁺ ions were quantified with atomic absorption spectroscopy, and the biomaterial performance was analyzed considering the adsorption capacity (, mmol/g) where is the residual concentration (mmol/L) quantified for the heavy metal ion in the aqueous solution after adsorption at given operating conditions. Adsorption capacities of both kinetic and equilibrium studies for all heavy metal ions and two biomaterials were calculated with equation (1).

2.3. Adsorption Modeling and Statistical Physics Calculations

The rates of adsorption of these heavy metal ions on SF and HH were calculated with the pseudo-second- and pseudo-first-order models [35]. The pseudo-first-order model is described with the following expression: where and (mmol/g) are the adsorption capacities at equilibrium and at time (min), respectively, and is the adsorption rate constant (min^-1). The pseudo-second-order equation is given by the following expression: where is the corresponding adsorption rate constant (g/mmol·min). Interested readers can found the explanation and fundaments of these kinetic models in the review [35]. A nonlinear regression was performed, and a comparison of the performance of these models was also done.

Thermodynamic parameters for the adsorption of Pb²⁺ ions with both keratin-based biomaterials were calculated using the van’t Hoff equation [36]. In particular, the changes of entropy (), enthalpy (), and free energy () of the adsorption of Pb²⁺ ion on HH and SF were calculated using the next equations [36–39]: where is the adsorption temperature (K), is the universal gas constant (8.314 J/mol K), and is the adsorption equilibrium constant calculated from the experimental Pb²⁺ ion adsorption studies. and were obtained from the linear regression of versus [36, 38] where was obtained from the distribution coefficient according to the procedure reported in [39] using the experimental Pb²⁺ ion adsorption data.

Recent studies have shown that a proper interpretation of adsorption mechanisms cannot be achieved using the traditional adsorption models (e.g., Sips and Langmuir) due to their parameters usually do not correspond to physicochemical variables for understanding this surface phenomenon [40]. Also, the complex composition of biomaterials could imply the presence of different interaction forces during the adsorption of heavy metal ions thus causing that the fundaments and theory of traditional adsorption models are not satisfied. Considering this fact, statistical physics modeling was implemented to analyze some physicochemical parameters associated with the adsorption mechanism of heavy metal ions on the surfaces of these keratinous biomaterials. This modeling analysis is useful to provide an understanding at macroscopic and microscopic scales of the adsorption system under analysis [41]. The adsorption orientation of heavy metal ions on the surfaces of the keratin-based materials was estimated with a statistical physics model. This statistical physics model assumed that each adsorption site (i.e., carboxyl or amino groups of keratin) of both biomaterials can accept a variable number of heavy metal ions where a monolayer of the adsorbed metal ions was formed on the keratin surface of HH and SF. This model is defined as [41] where represents the density of functional groups of the keratin surface involved in the adsorption (mmol/g), is the heavy metal ion concentration at equilibrium (mmol/L), is the number of heavy metal ions adsorbed per functional group available on the keratin surface of HH and SF, and is the heavy metal ion concentration at half-saturation (mmol/L), respectively. Herein, it is convenient to indicate that this statistical physics model has been used to analyze and interpret the adsorption of heavy metal ions in both natural and synthetic adsorbents [42, 43]. Interested readers are referred to the review [41] to understand the fundamentals and formulation of this statistical physics model.

Pb²⁺ ion adsorption data were correlated with the statistical physics model, which was selected as an adsorbate representative of tested heavy metal ions. This modeling approach has been proven to be helpful to provide insights and interpret the adsorption of heavy metal ions using different adsorbents [42–45]. Finally, the adsorption energy (, kJ/mol) of the Pb²⁺ ion adsorbent surface was calculated with the results of statistical physics models using the next expression [41]: where is the water solubility of the lead nitrate salt (mmol/L) used in the adsorption experiments.

3. Results and Discussion

3.1. Characterization of Keratin-Based Biomaterials

Table 1 displays the main physical properties determined for the two keratin-based biomaterials. pH of these adsorbents was 7.9 and 8.5 for HH and SF, respectively, while their moisture content ranged from 7.5 to 8.0%. Ignition mass losses were 76.6 and 97.9% for HH and SF, and they showed a bulk density of 0.0725 and 0.0298 g/cm³, respectively.

FTIR spectra of raw and metal-loaded HH and SF are shown in Figure 1, and Table 2 reports the interpretation of their main absorption bands. In general, the absorption spectra of both keratinous biomaterials after and before the adsorption of heavy metal ions were similar. In particular, the absorption band of N-H stretching was observed at 3308–3421 cm^-1. The bands appearing in the region of 2926–2962 cm^-1 were related to symmetrical CH₃ stretching vibration [46]. The band identified at 1649–1655 cm^-1 was associated with C=O stretching of amide I [47]. The absorption bands of amide II, which were the result of C-H stretching/N-H bending, can be observed at 1533–1541 cm^-1 [46, 48]. The absorption band of -CO stretching from the -COO- group was identified at ~1390 cm^-1 [48], and the changes in this band were associated with the interaction of carboxyl groups with heavy metal ions during adsorption. A weak band at 1236–1238 cm^-1 was identified and linked to the complex vibration containing N-H in-plane, C-O, and O=C=N bending plus C-N stretching, thus showing the presence of amide III [48–50]. The presence of C-S and S-S bonds in these biomaterials can be confirmed with bands at 914–930 cm^-1 [51]. The absorption band related to the C-S bond was also identified at 640 cm^-1 [52]. These results proved the protein nature of tested keratinous materials where some changes in the backbone structure of proteins were identified by amides I, II, and III [51].

SEM micrographs of HH and SF at 5000x magnifications are reported in Figure 2. The surface morphology of these keratinous biomaterials did not present significant differences before and after the removal of heavy metal ions. In general, these biomaterials showed a layer-like surface.

3.2. Adsorption of Heavy Metal Ions using HH and SF at Different Operating Conditions

Adsorption capacities of HH and SF can be affected by different operating parameters. In particular, the solution pH was relevant for heavy metal ion removal because it determined the biomaterial surface charge, metal ion solubility, ionization, and speciation [53]. Both SF and HH showed similar adsorption capacities for tested heavy metal ions at different pH conditions where pH 5 corresponded to the maximum removal (see Figure 3). Adsorption capacities of HH ranged from 0.026 to 0.388 mmol/g for Pb²⁺, 0.088 to 1.264 mmol/g for Cu²⁺, 0.035 to 1.331 mmol/g for Cr⁶⁺, and 0 to 0.125 mmol/g for Cd²⁺ at pH 1-5, while the SF adsorption capacities were 0.028–0.386 mmol/g for Pb²⁺, 0.098-1.196 mmol/g for Cu²⁺, 0.038-1.402 mmol/g for Cr⁶⁺, and 0-0.186 mmol/g for Cd²⁺ at the same operating conditions. All adsorption capacities decreased with solution pH until reaching a minimum value at pH 1 due to the metal ions competed with H⁺ for the functional groups on the keratin surface and the presence of repulsive electrostatic forces generated by the positively charged surfaces of HH and SF.

The impact of a biomaterial dose on the removal of heavy metal ions is reported in Figure 4. Results showed that the adsorption of these ions depended on this operating parameter where the pollutant removal increased with the biomaterial amount. Note that significant increments in the adsorption capacities were observed from 0.2 to 0.8 g/L where the biomaterial dose impact was less significant at >0.8 g/L. The increment of biomaterial amount increased the number of available functional groups of the keratin surface for the heavy metal ion removal thus generating better adsorption capacities [54, 55].

The adsorption kinetics of Cd²⁺, Pb²⁺, Cu²⁺, and Cr⁶⁺ ions on tested keratinous materials, using initial concentrations of 0.48 mmol/L at 298 K and pH 4, are reported in Figure 5. Overall, the adsorption capacities of all heavy metal ions for both biomaterials increased with the adsorption time until obtaining the solid-liquid equilibrium. The adsorption of these pollutants implied two stages: (1) a high and rapid initial adsorption of these adsorbates on keratin surface at <50 min and 2) a slower adsorption until reaching the equilibrium and biomaterial saturation at >100 min. The operating time to achieve this adsorption equilibrium was ~100 and 200 min for SF and HH, respectively. Both biomaterials were almost saturated at 100 min of contact time (see Figure 5). Adsorption kinetic modeling is reported in Table 3. The pseudo-first-order model fitted satisfactorily the kinetics of adsorption of heavy metal ions on SF where the adsorption rates ranged from 0.028 to 0.039 min^-1. Heavy metal ion kinetic data of HH were correlated satisfactorily with the pseudo-second order model where the calculated adsorption rates were 0.054–0.261 g/mmol·min.

Figure 6 reports the adsorption isotherms of all tested heavy metal ions for both SF and HH at pH 4 and 298 K. These results showed that the initial metal ion concentration increased the metal ion adsorption due to the mass transfer phenomena and a high probability of heavy metal ion-keratin surface interactions. Maximum adsorption capacities were 0.0704-1.4848 mmol/g for HH and 0.0926-1.5658 mmol/g for SF. The highest adsorption was obtained for Cr⁶⁺ ion using both biomaterials, while Cd²⁺ ion was the pollutant with the lowest adsorption capacities (see Figure 6). It could be expected that the electrostatic forces for the adsorption of Cr⁶⁺ ion were strongest than those for the other divalent heavy metal ions thus explaining the highest adsorption capacities obtained with both biomaterials.

Pb²⁺ ion was selected as a representative adsorbate of tested heavy metal ions to calculate its corresponding adsorption thermodynamic parameters at 20-50°C using both keratin-based biomaterials. Note that lead is a naturally occurring metal with several industrial applications, and consequently, it has been widely used as an adsorbate to study the removal of this type of pollutants with several materials [3, 4, 8]. Figure 7 shows that the adsorption of this heavy metal ion was endothermic for both HS and SF. The solution temperature is a relevant operating parameter that affected the transport and kinetic processes of heavy metal ion adsorption. Metal ion mobility and swelling effect within the internal structure of the biomaterials were associated with this parameter, and consequently, they affected the adsorption capacities [56]. For instance, the swelling effect can increase the number of functional groups of the keratin surface due to the expanding of microfibrous structure, thus enabling that metal ions can penetrate the biomaterial structure and enhance their removal.

Thermodynamic calculations of Pb²⁺ ion adsorption are reported in Table 4. Note that these thermodynamic parameters were obtained via a data correlation with . All calculated values were negative indicating that Pb²⁺ ion adsorption on SF and HH was a thermodynamically spontaneous process. Note that the spontaneity degree of adsorption of Pb²⁺ ions increased with temperature. values corresponded to an endothermic adsorption for both keratin-based biomaterials where the presence of both chemical and physical attraction forces could be expected [57]. Note that energy was required for the adsorbate to transfer through solution to the adsorption sites of keratin and get stripped out of their hydration shell [58]. for Pb²⁺ ion adsorption was 0.34 and 0.29 kJ/mol for SF and HH, respectively. These positive values were an indication of increased disorderliness at the biomaterial-liquid interface during the removal of these heavy metal ions, which could imply a dehydration of adsorbate before getting into the functional groups of biomaterials [59].

Finally, a comparison of the performance of these keratinous biomaterials with respect to other adsorbents used in the removal of heavy metal ions is provided in Table 5. Overall, HH and SF showed a competitive performance for the heavy metal ion removal, and they can outperform the adsorption capacities reported for different adsorbents. For instance, the Pb²⁺ and Cr⁶⁺ adsorption capacities of HH and SF were higher than those of a cysteine-modified biomass [60] and surfactant-modified coconut coir [61]. As stated, HH and SF are renewable and low-cost biomaterials thus offering additional advantages for their application in the water treatment.

Herein, it is convenient to remark that these biomaterials can be regenerated using acidic solutions to desorb the heavy metal ions loaded in their surfaces. This approach will allow the recovery of the adsorption properties of these adsorbents thus offering the possibility of reducing the costs of their application in water treatment. The spent biomaterial after reaching its lifetime should be properly disposed to avoid additional environmental pollution, or alternatively, they could be employed as a feedstock in other industrial processes (e.g., the manufacturing of polymer-based materials). Further studies in this direction are required to establish the best alternative for the final disposal of these biomaterials used in the adsorption of heavy metal ions.

3.3. Statistical Physics Calculations and Interpretation of the Adsorption Mechanism

Figure 7 also shows the results of statistical physics calculations for the Pb²⁺ ion adsorption isotherms of both HH and SF where was obtained. Table 6 reports the physicochemical parameters calculated with the statistical physics model, which were utilized to complement the analysis of the Pb²⁺ ion adsorption mechanism.

Statistical physics calculations indicated the parameter for the Pb²⁺ ion adsorption on HH. This result suggested that the adsorption of this metal ion on this keratinous biomaterial could be a multi-ionic process where Pb²⁺ ions interacted with one functional group from the keratin surface. For the case of SF, the values of this parameter ranged from 0.5 to 1 indicating that this heavy metal could be adsorbed on the SF surface via the interaction with one and two functional groups from keratin at the same time. The calculated density of functional groups of HH and SF surfaces that could be involved in the adsorption was 0.092-0.700 mmol/g at tested conditions. The calculated adsorption capacities of Pb²⁺ ion to achieve the biomaterial saturation () were 0.224-0.421 mmol/g for HH and 0.264-0.511 mg/g for SF. On the other hand, calculated adsorption energies ranged from 23.6 to 30.4 kJ/mol and from 23.3 to 30.0 kJ/mol for HH and SF, respectively. These calculations confirmed the endothermic nature of this adsorption process [41]. These adsorption energy values were consistent with the typical values of electrostatic interactions (10–50 kJ/mol) and coordination exchange (40 kJ/mol), which were the expected forces related to the adsorption mechanism of heavy metal ions with these biomaterials [36]. In particular, the adsorption of heavy metal ions on SF and HH surfaces can be represented by the next expressions:

where carboxyl and amino groups of keratin are expected to be involved in the adsorption of heavy metal ions [36, 41].

4. Conclusions

The thermodynamics and mechanism interpretation of the adsorption of heavy metal ions on human hair and sheep were analyzed and discussed. These keratin-based biomaterials achieved adsorption capacities up to 1.4 mmol/g for the heavy metal ion removal from aqueous solutions. Both biomaterials showed the highest adsorption capacities for chromium ions (1.48 and 1.57 mmol/g with HH and SF, respectively), while the lowest adsorption capacities were obtained for cadmium ions (0.07 and 0.09 mmol/g with HH and SF, respectively). Adsorption of heavy metal ions with both keratinous materials was highly pH dependent, and the adsorption capacities were reduced up to 98% at pH 1. A detailed analysis of lead ion adsorption was performed, and results indicated that the removal of this heavy metal ion was endothermic for both biomaterials with adsorption enthalpies of 85–97 kJ/mol. Statistical physics calculations suggested the occurrence of a multi-ion process in lead ion adsorption especially for human hair and confirmed the endothermic nature of this removal process. These biomaterials showed competitive adsorption capacities and can outperform commercial activated carbons and other adsorbents reported in literature. Therefore, they are an alternative to prepare composites and functionalized materials for achieving the goal of a low-cost and sustainable wastewater treatment.

Data Availability

Data of this paper are available on request to the corresponding author.

Conflicts of Interest

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Acknowledgments

MB acknowledges the financial support through the COMETE project (COnception in silico de Matériaux pour l’EnvironnemenT et l’Energie) cofunded by the European Union under the program “FEDER-FSE Lorraine et Massif des Vosges 2014-2020.” ABP is also thankful to the University of Lorraine for the invited professorship in the academic year 2020-2021.

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Copyright © 2022 Salaudeen Abdulwasiu Olawale et al. 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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