Dimercaptosuccinic Acid Functionalized Polystyrene Column for Trace Concentration Determination of Heavy Metal Ions: Experimental and Theoretical Calculation Studies

: Metal ion studies in wastewater are required on a regular basis for environmental monitoring and assessment. Less metal ion concentrations and the interference from complex sample matrices remains challenging for instrumental quantiﬁcation. Herein, we proposed a ﬁx-bed solid phase extraction method, consisting of a newly prepared dimercaptosuccinic acid functionalized polystyrene beads. The ligand forms stable complex with Hg(II), Pb(II), and Cd(II), evident by experimental as well as density functional theory. The metal-ligand stabilization energy calculations, suggested the higher selectivity of polystyrene dimercaptosuccinic acid (PSDMSA) toward Pb(II) compared to Cd(II) and Hg(II). The prepared adsorbent was utilized to enrich Hg(II), Pb(II), and Cd(II) ions from environmental samples. Column parameters were studied in detail and optimized accordingly. The preconcentration factor for Hg(II), Pb(II), and Cd(II) were found to be 900, with the preconcentration limit of 0.74 µ g L − 1 . The detection limit for Pb(II), Cd(II), and Hg(II) ions was found to be 1.3 ± 0.2, 1.5 ± 0.3, and 1.8 ± 0.3 ng L − 1 , respectively. The method accuracy was tested against systematic and continuous errors by standard addition method (<5% RSD). Real samples was successfully analyzed following the proposed method.


Introduction
Water pollution because of the discharge of heavy metals in various forms into environmental water streams by various industrial sources has grown to be one of many concerns worldwide. Mercury (Hg), lead (Pb), and cadmium (Cd) ranked noxious among all hazards contained in the toxic waste sites at national priority list by the Agency for Toxic Substances and Disease Registry (ASTDR) [1]. The acceptable limits in drinking water for these metal ions are 2, 15, and 5 µg L −1 , respectively [2]. These heavy metal ions, alone or in combination, constitute a severe hazard to biota and human health [3][4][5][6][7]. Therefore, environmental monitoring to test their contamination level and assessment of the exposure are one of the top priorities acquiesced by WHO (World Health Organization) [8,9]. It is essential to develop sensitive, accurate, and economical means to analyze environmental water samples [10][11][12][13][14]. Metal-ligand complex formation is of special significance where a specific ligand can selectively coordinate with the heavy metal ions in order to extract Water 2021, 13, 3056 2 of 12 them from the complex sample matrix [3]. In solid phase extraction (SPE), research has been focused on the preparation of new adsorbent materials including polymeric materials, nano-materials, metal-organic framework, and carbonaceous materials for wastewater remediation [15][16][17][18][19][20]. Polymeric adsorbents has been considered as a promising material, since it has an advantage of column operation over nano-materials, and widely acceptable in water treatment techniques [21][22][23][24][25]. Although several nano-materials have been reported either in the batch mode or column operations [26][27][28][29][30]. However, due to very small size (nm) and high dispersity, the use of nano-materials in column operations may lead to adsorbent leaching during column experiments. Furthermore, the release of nanomaterials may cause toxicity to ecosystem [31,32] and requires another developed method for their extraction.
In this work, the authors synthesized a new adsorbent fabricated by the functionalization of chloromethylated polystyrene resin by a dimercaptosuccinic acid (DMSA) ligand in single step (PSDMSA). DMSA, a bidentate ligand possess two carboxylic and two thiol functionality ( Figure 1). DMSA selectively binds to heavy metal ions either through the two mercapto groups or one carboxyl and one mercapto group. The sulfur atoms of the thiol groups in DMSA have a higher complexation ability for Hg(II), Pb(II), and Cd(II) ions. The selectivity and coordination mechanism of prepared PSDMSA sorbent for Hg(II), Pb(II), and Cd(II) have been studied via experimental as well as DFT studies and reported in this work. The polystyrene resin with high surface area and porosity after functionalization leads to high selectivity toward the studied metal ions. The prepared PSDMSA sorbent was successfully utilized in the preconcentration of metal ions from the environmental samples.
Water 2021, 13, x FOR PEER REVIEW 2 of 13 extract them from the complex sample matrix [3]. In solid phase extraction (SPE), research has been focused on the preparation of new adsorbent materials including polymeric materials, nano-materials, metal-organic framework, and carbonaceous materials for wastewater remediation [15][16][17][18][19][20]. Polymeric adsorbents has been considered as a promising material, since it has an advantage of column operation over nano-materials, and widely acceptable in water treatment techniques [21][22][23][24][25]. Although several nano-materials have been reported either in the batch mode or column operations [26][27][28][29][30]. However, due to very small size (nm) and high dispersity, the use of nano-materials in column operations may lead to adsorbent leaching during column experiments. Furthermore, the release of nano-materials may cause toxicity to ecosystem [31,32] and requires another developed method for their extraction.
In this work, the authors synthesized a new adsorbent fabricated by the functionalization of chloromethylated polystyrene resin by a dimercaptosuccinic acid (DMSA) ligand in single step (PSDMSA). DMSA, a bidentate ligand possess two carboxylic and two thiol functionality (Figure 1). DMSA selectively binds to heavy metal ions either through the two mercapto groups or one carboxyl and one mercapto group. The sulfur atoms of the thiol groups in DMSA have a higher complexation ability for Hg(II), Pb(II), and Cd(II) ions. The selectivity and coordination mechanism of prepared PSDMSA sorbent for Hg(II), Pb(II), and Cd(II) have been studied via experimental as well as DFT studies and reported in this work. The polystyrene resin with high surface area and porosity after functionalization leads to high selectivity toward the studied metal ions. The prepared PSDMSA sorbent was successfully utilized in the preconcentration of metal ions from the environmental samples.

Reagents and Solutions
The resin beads and DMSA were purchased from Merck (Steinheim, Germany). All metal ions solutions used (1000 ppm) was obtained from Merck (Beijing, China). The model solutions of desired concentrations were prepared from stock solution after dilution. All glassware's were dipped overnight in 2% nitric acid solution before use.

Equipments
The incorporation of ligand was confirmed by the Fourier transformed infrared spectroscopy (FT-IR, Perkin Elmer, Waltham, MA, USA). The elemental constituents was analyzed using energy dispersive X-ray analysis (Bruker, Germany). The surface area measurements was carried out using Quanta chrome equipment (Boynton Beach, FL, USA) using nitrogen gas. A Zetasizer (Malvern Instruments, Malvern, UK) was used to study zeta potential (z). The concentrations of Hg(II), Pb(II) and Cd(II) was analyzed by inductively

Reagents and Solutions
The resin beads and DMSA were purchased from Merck (Steinheim, Germany). All metal ions solutions used (1000 ppm) was obtained from Merck (Beijing, China). The model solutions of desired concentrations were prepared from stock solution after dilution. All glassware's were dipped overnight in 2% nitric acid solution before use.

Equipments
The incorporation of ligand was confirmed by the Fourier transformed infrared spectroscopy (FT-IR, Perkin Elmer, Waltham, MA, USA). The elemental constituents was analyzed using energy dispersive X-ray analysis (Bruker, Germany). The surface area measurements was carried out using Quanta chrome equipment (Boynton Beach, FL, USA) using nitrogen gas. A Zetasizer (Malvern Instruments, Malvern, UK) was used to study zeta potential (z). The concentrations of Hg(II), Pb(II) and Cd(II) was analyzed by inductively coupled plasma optical emission spectrophotometer (ICP-OES, Perkin Elmer, Waltham, MA, USA; model Avio 200).

Computational Studies
The quantum mechanics was applied to compute the geometries, chemical stability, bond lengths, stabilization energies, and binding energies of the free PSDMSA and metalcoordinated PSDMSA and considering water as a solvent. The calculations were performed using the Gaussian 09 software package [33]. For C, O, S, and H elements, the B3 LYP command with the 6-311++G basis set was employed and the LANL2 DZ basis set for metal ions was used [34,35]. The solvent effect was simulated by the conductor polarizable continuum model (CPCM) [36].

Synthesis of PSDMSA Adsorbent
The chloromethylated polystyrene (PS) beads were chemically functionalized with DMSA ligand by a simple condensation procedure, followed by nucleophile addition to eliminate HCl molecules. In brief, 10.0 g of PS beads was soaked overnight with 50 mL of dimethylformamide (DMF). A 10 mL solution of DMSA (1.5 g), prepared in DMF was added to the PS solution. The whole content was bath sonicated for 15 min to mix the two components. Afterward, the whole components was refluxed (with stirring) for 2.0 h at 70 • C with triethylamine (TEA catalyst) to remove the HCl bi-product. The product was cooled down and filtered off by using a 0.22 µm filter paper. The obtained PSDMSA was sequentially cleaned with DMF, ethanol, and deionized (DI) water to remove the reacted DMSA ligand. The PSDMSA was oven dried at 50 • C for 12 h before further use. The synthesis scheme for single unit is presented in Figure 1.

Batch Studies
The batch experiment was conducted by equilibrating the 100 mg of PSDMSA adsorbent with individual metal ions (500 ppm) in a 100 mL Erlenmeyer flask, at different sample pH (1-7). The shaking (equilibrium) time for each metal ions was 24 h. Afterward, the concentration of remaining (un-adsorbed) analytes was determined using ICP-OES to measure the uptaken metal ions. The uptaken metal ions at varying sample pH (Figure 2A), were observed by using the given equation: where, C i and C f -concentration of loaded and left metal ions (mg L −1 ), respectively; Vsample volume (L) and m-adsorbent mass (g). The metal ions uptaken capacity of PDMSA was 0.75 for Hg(II), 0.62 for Pb(II) and 0.66 mmol g −1 for Cd(II), at optimum pH value of 6.0 ± 0.2. In Figure 3 were observed zeta potential studies. In Figure 3 were observed zeta potential studies. In Figure 3 were observed zeta potential studies. Figure 3. Zeta potential of PSDMSA adsorbent (sample volume 100 mL; sorbent dose 100 mg).

Column Procedure for Metal Ions Preconcentration
Individual model solution (100 mL) for Hg(II), Pb(II), and Cd(II) ions, at concentration of 10 μg L −1 , was set to pH 6.0±0.2. The model solutions was passed through a glass column possess 100.0 mg of PSDMSA adsorbent, at the flow rate of 5 mL min −1 , optimized by peristaltic pump (Millipore XI0422050, Beijing, China). The concentration of uptaken metal ions was determined by ICP-OES after elution with 3 mL of 1 M hydrochloric acid.

Characterization of PSDMSA
The incorporation of surface functional groups onto PS beads was observed and confirmed by fourier transform infrared spectroscopy (FTIR) analysis. In the FTIR spectra ( Figure 4), a peak at 3200-3500 cm −1 attributes to presence of -OH group of carboxylic acid of the DMSA ligand. The strong peak at 1700 cm −1 confirms to C = O groups. The peak at 1350 cm −1 ascertain the C-O stretching. The peak at 2900 cm −1 represents the -CH stretching vibrations of aromatic carbon of the PS beads, respectively. The prominent bands obtained at 3250 cm −1 and 1025 cm −1 are corresponds to -OH and -SH stretching vibrations, and confirm the successful immobilization of ligand. The nitrogen gas adsorption-desorption isotherm is shown in Figure 5. The surface area of PSDMSA, estimated by multipoint BET method, was observed to 44.15 m 2 g −1 . The elemental mapping of the prepared

Column Procedure for Metal Ions Preconcentration
Individual model solution (100 mL) for Hg(II), Pb(II), and Cd(II) ions, at concentration of 10 µg L −1 , was set to pH 6.0 ± 0.2. The model solutions was passed through a glass column possess 100.0 mg of PSDMSA adsorbent, at the flow rate of 5 mL min −1 , optimized by peristaltic pump (Millipore XI0422050, Beijing, China). The concentration of uptaken metal ions was determined by ICP-OES after elution with 3 mL of 1 M hydrochloric acid.

Characterization of PSDMSA
The incorporation of surface functional groups onto PS beads was observed and confirmed by fourier transform infrared spectroscopy (FTIR) analysis. In the FTIR spectra ( Figure 4), a peak at 3200-3500 cm −1 attributes to presence of -OH group of carboxylic acid of the DMSA ligand. The strong peak at 1700 cm −1 confirms to C=O groups. The peak at 1350 cm −1 ascertain the C-O stretching. The peak at 2900 cm −1 represents the -CH stretching vibrations of aromatic carbon of the PS beads, respectively. The prominent bands obtained at 3250 cm −1 and 1025 cm −1 are corresponds to -OH and -SH stretching vibrations, and confirm the successful immobilization of ligand. The nitrogen gas adsorptiondesorption isotherm is shown in Figure 5. The surface area of PSDMSA, estimated by multipoint BET method, was observed to 44.15 m 2 g −1 . The elemental mapping of the prepared PSDMS A after metal ions adsorption was obtained from the energy dispersive X-ray spectroscopy ( Figure 6), and depicts the successful adsorption of metal ions.
Water 2021, 13, x FOR PEER REVIEW 5 of 13 PSDMS A after metal ions adsorption was obtained from the energy dispersive X-ray spectroscopy ( Figure 6), and depicts the successful adsorption of metal ions.    PSDMS A after metal ions adsorption was obtained from the energy dispersive X-ray spectroscopy ( Figure 6), and depicts the successful adsorption of metal ions.

Effect of Sample pH
The sample pH is an important parameter for metal-ligand complexation. The effect of sample pH on Hg(II), Pb(II), and Cd(II) adsorption by PSDMSA, was studied by batch adsorption strategy. Details are given in Section 2.4. For comparative studies, a nascent PS was also studied for metal ions adsorption following the same procedure as for PSDMSA. The adsorption trend for PSDMSA is shown in Figure 2. For nascent PS adsorbent, no significant adsorption was observed at all pH values ( Figure 2B). The functional groups of PSDMSA gets protonated with positive charge at acidic pH values of 1-2, which reduced the chelating capacity with metal ions. This might be because metal ions repel protonated binding sites electrostatically. However, at higher pH values, the adsorption of metal ions significantly increases with the increase of pH from 3-7. This may be due the dissociation of the H + ions, which reduces the positive charge density on functional groups and thus, increases the coordination ability of ligand with the metal ions. This was also observed from zeta potential studies (Figure 3). Another important factor, promoting the metal ions adsorption is Lewis soft-soft interaction. According to Pearson's Hard and Soft acid base theory Pb(II), Cd(II), and Hg(II) are the soft acids and form favorable complexes with the soft base (thiol groups) of the ligands [37,38]. In conclusion, at optimal pH levels, inner-sphere surface chelation dominates strong metal ion sorption, rather than physical adsorption [39]. Hence, pH 6 was optimized for the adsorption of metal ion in all further experiments. Furthermore, the stability order of metal-PSDMSA complexes is also evidenced by following the theoretical studies.

Theoretical Validation
The optimized structures of PSDMSA and Me-PSDMSA with their structural parameters are presented in Figures 7 and 8. It is assumed that the PSDMSA forms two possible complexes with metal ions either by one −COOH and one −SH group (complex 1) OR by two -SH groups (complex 2). Only the simplest complexes 1 and 2 were calculated. The tridentate and tetra dentate complexes are not studied in this article. Comparison associated with the bond length of free PSDMSA and metal affiliated complexes reveals that the C-O and C-S bond distances of PSDMSA varies on complex formation (Table 1). Moreover, in Me-PSDMSA complexes the Me-S and Me-O bond lengths for Pb(II), Cd(II), and Hg(II) for both the complexes type are mentioned in Table 1. The obtained data suggest that, in complex 1 and 2, Cd(II) and Hg(II) forms stronger complexes with PSDMSA than Pb(II). Moreover, in complex 1, the average Me-S distances for Pb(II), Cd(II), and Hg(II) complexes are 2.584, 1.521, and 1.521 Å, respectively, which are less than those of average Me-S distances in complex 2. This indicates that the interaction between metal ions and

Effect of Sample pH
The sample pH is an important parameter for metal-ligand complexation. The effect of sample pH on Hg(II), Pb(II), and Cd(II) adsorption by PSDMSA, was studied by batch adsorption strategy. Details are given in Section 2.4. For comparative studies, a nascent PS was also studied for metal ions adsorption following the same procedure as for PSDMSA. The adsorption trend for PSDMSA is shown in Figure 2. For nascent PS adsorbent, no significant adsorption was observed at all pH values ( Figure 2B). The functional groups of PSDMSA gets protonated with positive charge at acidic pH values of 1-2, which reduced the chelating capacity with metal ions. This might be because metal ions repel protonated binding sites electrostatically. However, at higher pH values, the adsorption of metal ions significantly increases with the increase of pH from 3-7. This may be due the dissociation of the H + ions, which reduces the positive charge density on functional groups and thus, increases the coordination ability of ligand with the metal ions. This was also observed from zeta potential studies (Figure 3). Another important factor, promoting the metal ions adsorption is Lewis soft-soft interaction. According to Pearson's Hard and Soft acid base theory Pb(II), Cd(II), and Hg(II) are the soft acids and form favorable complexes with the soft base (thiol groups) of the ligands [37,38]. In conclusion, at optimal pH levels, inner-sphere surface chelation dominates strong metal ion sorption, rather than physical adsorption [39]. Hence, pH 6 was optimized for the adsorption of metal ion in all further experiments. Furthermore, the stability order of metal-PSDMSA complexes is also evidenced by following the theoretical studies.

Theoretical Validation
The optimized structures of PSDMSA and Me-PSDMSA with their structural parameters are presented in Figures 7 and 8. It is assumed that the PSDMSA forms two possible complexes with metal ions either by one −COOH and one −SH group (complex 1) OR by two -SH groups (complex 2). Only the simplest complexes 1 and 2 were calculated. The tridentate and tetra dentate complexes are not studied in this article. Comparison associated with the bond length of free PSDMSA and metal affiliated complexes reveals that the C-O and C-S bond distances of PSDMSA varies on complex formation (Table 1). Moreover, in Me-PSDMSA complexes the Me-S and Me-O bond lengths for Pb(II), Cd(II), and Hg(II) for both the complexes type are mentioned in Table 1. The obtained data suggest that, in complex 1 and 2, Cd(II) and Hg(II) forms stronger complexes with PSDMSA than Pb(II). Moreover, in complex 1, the average Me-S distances for Pb(II), Cd(II), and Hg(II) complexes are 2.584, 1.521, and 1.521 Å, respectively, which are less than those of average Me-S distances in complex 2. This indicates that the interaction between metal ions and PSDMSA in complex 1 is stronger than complex 2. It is concluded that the carboxylic/thiol groups (Complex 1) have high affinity for metal ion complexation and act as the primary metal ion binding sites in PSDMSA than thiol/thiol groups.
PSDMSA in complex 1 is stronger than complex 2. It is concluded that the carboxylic/thiol groups (Complex 1) have high affinity for metal ion complexation and act as the primary metal ion binding sites in PSDMSA than thiol/thiol groups.
Natural bond order (NBO) analysis was performed to investigate the charge transfer phenomenon between the functional groups of PSDMSA and metal ions during complexation. The binding (Ebind) and stabilization energies (E) were calculated and are reported in Table 2. The larger E value of M-L complex represents a higher stability. From Table 2, Pb-PSDMSA complex shows the highest stabilization energy value, suggested the higher selectivity of PSDMSA toward Pb(II) in comparison to Cd(II) and Hg(II).   PSDMSA in complex 1 is stronger than complex 2. It is concluded that the carboxylic/thiol groups (Complex 1) have high affinity for metal ion complexation and act as the primary metal ion binding sites in PSDMSA than thiol/thiol groups.
Natural bond order (NBO) analysis was performed to investigate the charge transfer phenomenon between the functional groups of PSDMSA and metal ions during complexation. The binding (Ebind) and stabilization energies (E) were calculated and are reported in Table 2. The larger E value of M-L complex represents a higher stability. From Table 2, Pb-PSDMSA complex shows the highest stabilization energy value, suggested the higher selectivity of PSDMSA toward Pb(II) in comparison to Cd(II) and Hg(II).    Natural bond order (NBO) analysis was performed to investigate the charge transfer phenomenon between the functional groups of PSDMSA and metal ions during complexation. The binding (E bind ) and stabilization energies (E) were calculated and are reported in Table 2. The larger E value of M-L complex represents a higher stability. From Table 2, Pb-PSDMSA complex shows the highest stabilization energy value, suggested the higher selectivity of PSDMSA toward Pb(II) in comparison to Cd(II) and Hg(II).

Optimized Flow Rate
A sample solution (50 mL) with 10 µg of each metal ion was run at varied sample flow rates of 2-10 mL min −1 to optimize the column flow rate for metal ion adsorption. Figure 9 shows that the adsorption of Pb(II), Cd(II), and Hg(II) were accomplished satisfactorily up to a sample flow rate of 5 mL min −1 . When the sample flow was increased to 6-8 mL min −1 , there was a 6-10% drop in Pb(II) adsorption and an 8-15% decrease in Cd(II) and Hg(II) adsorption. The reduction in metal ion adsorption with increased sample flow might be attributed to shorter chelation time for the metal-ligand coordination. As a result, 5 mL min −1 of sample flow was optimized and used for sample analysis.

Optimized Flow Rate
A sample solution (50 mL) with 10 μg of each metal ion was run at varied sample flow rates of 2-10 mL min −1 to optimize the column flow rate for metal ion adsorption. Figure 9 shows that the adsorption of Pb(II), Cd(II), and Hg(II) were accomplished satisfactorily up to a sample flow rate of 5 mL min −1 . When the sample flow was increased to 6-8 mL min −1 , there was a 6-10% drop in Pb(II) adsorption and an 8-15% decrease in Cd(II) and Hg(II) adsorption. The reduction in metal ion adsorption with increased sample flow might be attributed to shorter chelation time for the metal-ligand coordination. As a result, 5 mL min −1 of sample flow was optimized and used for sample analysis.

Co-Ions Interferences and Desorption Studies
In the preconcentration of analyte metal ions, associated co-existing ions such as alkali and alkaline earth metals often interfere. They might compete with metal ions and interfere in the complexation reaction, thereby reducing the analyte adsorption. Moreover, these concomitants along with analyte ions cause the interference in the instrumental analysis. The ionic concentrations varied >±5% in the preconcentration of analyte ions were considered to be the interferents. Aliquots (100 mL) containing individual metal ion (10 µg) and high concentrations of concomitants were tested. The adsorbed metal ions were eluted and sequentially analyzed by ICP-OES. Results are shown in (Table 3). It was observed that the percent recovery of analytes are well above 96%, indicating that there were no significant interferences by concomitants in the analysis of target ions.
Desorption of metal ions from column bed was performed using HCl and HNO 3 with varying concentrations (0.5-2.0) and volumes (1-5 mL). We found that 1 M HCl (3 mL) would completely elute the Pb(II), Cd(II) and Hg(II) ions, from the column bed with >99% extraction. Therefore, 3 mL of 1 M HCl was optimized for stripping of metal ions.

Preconcentration Studies
Samples with varying sizes (1500, 2000, 2500, 2700, 3000, and 3200 mL at pH 6.0) containing 2 µg of individual metal ions were flowed through PSDMSA packed column at a flow rate of 5 mL min −1 . The effluent collected was discarded. The adsorbed metal ions was eluted and the concentration of metal ions was analyzed by ICP-OES. From the obtained data it was found that Pb(II), Cd(II), and Hg(II) ions were quantitatively recovered up to a sample volume of 3000 mL with metal ions recovery of 99.0 ± 5%, therefore, suggesting a preconcentration limit of 0.74 µg L −1 , with the preconcentration factor of 900 (2700 mL sample divided by 3 mL eluent). At sample volume of 3000 mL, the analyte adsorption was reduced to 92% for Pb(II) and Cd(II) and 85% for Hg(II). Because of the increased preconcentration factor, the adsorbent might be used with any detection approach, whether offline or online. The presence of a high number of hydrophilic groups on the adsorbent increased the preconcentration factor by making it easier to achieve equilibrium between active sites and metal ions in aqueous solutions.

Analytical Figures of Merits
After the preconcentration operation, the calibration plots were linear in the range of 0.01-100 µg L −1 . The correlation coefficient (R 2 ) obtained was at least 0.999. To ensure accuracy, the standard addition procedure was used. With a RSD (relative standard deviation) value of 3.5-5%, the recovery of spiked amounts (Pb, Cd, Hg) were close to 99.9%. Table 4 displays the findings. At a 95% confidence level, the Student's t-test values determined here, were found smaller than the critical t values (4.303, n = 5) ( Table 4). Five repeated analysis with 5 µg of analyte ions with 50 mL solutions were used to validate the method's accuracy. The method's accuracy is shown by the lower value of coefficients of variation (5%). The slope of the calibration curves is referred to as sensitivity. The method LOD (limit of detection) for Pb(II), Cd(II), and Hg(II) ions, calculated as 3s/m (s-standard deviation; m slope), were determined to be 1.3 ± 0.2, 1.5 and 1.8 ± 0.3 ng L −1 , respectively.

Application of the Method
Three environmental samples were subjected to the devised preconcentration method. The sorbed metal ions were eluted and examined by ICP-OES after preconcentration. Table 4 shows the amounts of Pb(II), Cd(II), and Hg(II) measured in genuine samples. The analytes that were retained were analyzed with a 95% confidence interval. With a RSD of 3.5-4.5%, the mean percent recoveries vary from 98.7-102%. With an average error of 3%, the new method demonstrated high repeatability.

Conclusions
We proposed a new SPE column packed with thiol-immobilized polystyrene grains for the selective extraction of metal ions. The sorption behaviors of the prepared sorbent was evaluated for toxic metal ions. The sorbent shows efficient and fast sorption behavior in aqueous solutions. The proposed method shows the fair preconcentration limit of 0.74 µg L −1 , for Hg(II), Pb(II), and Cd(II). The metal ions sorption mechanism was revealed by studying the effect of sample pH. The E bind value for Pb(II) (−118.227 Kcal mol −1 ) was higher than the E bind of Cd(II) (−42.164 Kcal mol −1 ) and Hg(II) (−35.603 Kcal mol −1 ), suggesting that the PSDMSA forms more stable complex with Pb(II) compared to Cd(II) and Hg(II) ions. A comparative data of this study with other reported methods has been provided in Table 5, to make the manuscript potential for the valued readers. The obtained results highlights the usefulness of surface functionalization and expands the potential applicability of the prepared column for selective extraction and routine analysis of toxic metal ions from real samples.