Investigation about the copper adsorption on the chloropropylsilica gel surface modified with a nanostructured dendrimer DAB-Am-16: an analytical application for determination of copper in different samples

Abstract

The third generation (G-3) poly(propyleneimine)hexadecaamine dendrimer (DAB-Am-16) was grafted onto the chloropropylsilica gel surface (DPPIPS). The modified silica (DPPIPS) was characterized by Electronic (Uv-Vis), vibrational and Electron Paramagnetic Resonance (EPR), spectrocopies, surface area (331.07 m².g-1) and porosity analyses (pore diameter of 41.9 nm) and cyclic voltammetry technique. The copper adsorption studies were performed using a batchwise process and the DPPIPS showed adsorption capacities of 16.3, 47.8 and 659.5 mol.g-1 in aqueous, ethanol and acetone medium, respectively, with recoveries close to 100% after percolation with HCl 1.0 mol.L-1. The results suggest that the sorption of copper ions on DPPIPS occurs mainly by surface complexation and a Langmuir model allowed describing the sorption of the metal ions on DPPIPS. As an application of this chemically modified material, copper was determined in real samples of distilled spirits and fuel alcohol.

adsorption; dendrimer; silica; spectroscopy; chemical synthesis

Investigation about the copper adsorption on the chloropropylsilica gel surface modified with a nanostructured dendrimer DAB-Am-16: an analytical application for determination of copper in different samples

Devaney Ribeiro do Carmo^I,*; Leonardo Lataro Paim^II

^IDepartamento de Física e Química, Faculdade de Engenharia de Ilha Solteira, Universidade Estadual Paulista – UNESP, Av. Brasil, 56, Centro, CEP 15385-000, Ilha Solteira, SP, Brasil

^IIInstituto de Química de Araraquara, Universidade Estadual Paulista – UNESP, Rua Francisco Degni, 55, CEP 14801-970, Araraquara, SP, Brasil

ABSTRACT

The third generation (G-3) poly(propyleneimine)hexadecaamine dendrimer (DAB-Am-16) was grafted onto the chloropropylsilica gel surface (DPPIPS). The modified silica (DPPIPS) was characterized by Electronic (Uv-Vis), vibrational and Electron Paramagnetic Resonance (EPR), spectrocopies, surface area (331.07 m².g^–1) and porosity analyses (pore diameter of 41.9 nm) and cyclic voltammetry technique. The copper adsorption studies were performed using a batchwise process and the DPPIPS showed adsorption capacities of 16.3, 47.8 and 659.5 mol.g^–1 in aqueous, ethanol and acetone medium, respectively, with recoveries close to 100% after percolation with HCl 1.0 mol.L^–1. The results suggest that the sorption of copper ions on DPPIPS occurs mainly by surface complexation and a Langmuir model allowed describing the sorption of the metal ions on DPPIPS. As an application of this chemically modified material, copper was determined in real samples of distilled spirits and fuel alcohol.

Keywords: adsorption, dendrimer, silica, spectroscopy, chemical synthesis

1. Introduction

Dendrimers are well-defined, hyperbranched macromolecules with a high concentration of peripheral chain ends¹. Many of the properties of these molecules are strongly influenced by these end groups. These novel materials have established their importance in the modern synthetic chemistry². Moreover, the multi-functional groups (branches) endow dendrimers with special properties. Dendrimers are used in drugs delivery and carriers^3-6, fuel cells⁷, light-emitting diodes^8,9, liquid crystals¹⁰ and chemical modifications^11,12, membrane separation¹³. In nowadays, most investigators have focused their attentions on the free dendrimers, while the properties and applications of other kinds of supported dendrimers are seldom reported.

DAB-Am-16 also known by Poly(propylene imine) dendrimer (DPPI) and when terminated with fatty acids, for example, behave like inverted unimolecular dendritic micelles that consist of a polar core and an apolar periphery¹⁴. In DAB-Am-16, there are three generations of branches, and the outermost shell is composed of 16-NH₂ groups. These 16-NH₂ groups are susceptible for different reactions. Silica was chosen as substrate for anchoring DAB-Am-16 due to high stability of complexes formed that permit their multiple uses in preconcentration and separation processes.

Of particular interest has been the use of this modified silica in sorbing metal ions from aqueous or non-aqueous solutions¹⁵ and in electroanalysis¹⁶. In solution phase, many complex species may be formed on the solid surface by the reaction of metal ions with immobilized organic molecules. However, some limitations are imposed on the complexes formed at the solid-solution interface, since the attached ligands have limited mobility or are suitable to leach. The stepwise complex formation, which consists of a change in the number of attached ligands coordinating one metal ion, is therefore a function of the surface loading of the support^17-19.

Heidari et al.¹⁷ applied mesoporous silica materials for the removal of Ni(II), Cd(II) and Pb(II) ions from aqueous solution. The effects of the solution pH, metal ion concentrations, adsorbent dosages, and contact time were studied for MCM-41, nanoparticle of MCM-41, NH₂-MCM-41 (amino functionalized MCM-41) and nano NH₂-MCM-41. NH₂-MCM-41 showed the highest uptake for metal ions in aqueous solution and the maximum adsorption capacity of NH₂-MCM-41 for Ni(II), Cd(II) and Pb(II) was found to be 12.36, 18.25 and 57.74 mg.g^–1, respectively. The experimental data were analyzed using the Langmuir and Freundlich equations and theirs correlation coefficients were determined by analyzing each isotherm. The Langmuir equation showed better correlation with the experimental data than the Freundlich.

Shahbazi et al.¹⁸ used a functionalized SBA-15 mesoporous silica with polyamidoamine groups (PAMAM-SBA-15) for the removal of Cu(II), Pb(II) and Cd(II) ions from aqueous solution. The effects of the solution pH, adsorbent dosage and metal ion concentration were studied under the batch mode. The Langmuir model was fitted favorably to the experimental data. The maximum sorptive capacities were determined to be 1.74 mmol.g^–1 for Cu(II), 1.16 mmol.g^–1 for Pb(II) and 0.97 mmol.g^–1 for Cd(II). The adsorbent could be regenerated three times without significant varying its sorption capacity. A series of column tests were performed to determine the breakthrough curves with varying bed heights and flow rates. Maximum sorption capacity of 1.6, 1.3 and 1.0 mmol.g^–1 were found for Cu(II), Pb(II) and Cd(II), respectively, at flow rate of 0.4 mL/min and bed height of 8 cm, which corresponds to 83%, 75% and 73% of metallic ion removal, respectively, which very close to the value determined in the batch process.

In another work, Shahbazi et al.¹⁹ used the SBA-15 mesoporous silica modified with amine (–NH2) and melamine-based dendrimer amines (MDA) for studied the adsorption of Pb(II), Cu(II) and Cd(II) ions. The equilibrium data were analyzed using the Langmuir and Freundlich isotherm by nonlinear regression analysis. The kinetics analysis revealed that the overall adsorption process was successfully fitted with the pseudo-first-order kinetic model. The adsorption of Pb(II), Cu(II) and Cd(II) onto MDA–SBA-15 was strongly dependent on temperature, and the adsorption capacity decreased with increasing the temperature of the system, indicating the exothermic and spontaneous nature of adsorption. MDA–SBA-15 was regenerated and found to be suitable for reuse in successive adsorption-desorption cycles four times without significant loss in adsorption capacity. The results suggested that MDA–SBA-15 can be used as an adsorbent for an efficient removal of metal ions from aqueous solution.

The advantage of using dendrimers to make dendrimer supported silica is 2-fold: First, DAB-Am-16 can be used as heterogeneous catalyst. Second, the chelating capacity of such amine dendrimers can be used to adsorb metal ions in the environmental and biological samples in organic or aqueous medium because amine dendrimers are macrochelating agents for transitions metals. Like polymers, dendrimers have a large number of functional groups, with which they can attach to the different surface such as Silica gel. In this context, this work have as purpose to prepared dendrimer supported on the silica gel surface to analytical and electroanalytical application, using a direct and facile procedure.

2. Experimental

2.1. Reagents

All chemicals were of analytical reagent grade. All solutions and supporting electrolytes were prepared using doubly-demineralized water obtained by passing distilled water through a Millipore Milli-Q water purification system. The other reagents and solvents were of analytical grade (Sigma-Aldrich, Merck) and were used as purchased.

2.2. Synthesis

2.2.1. Preparation of 3-chloropropylsilica gel

Silica gel (Merck), particle size 0.05-0.2 mm and 60 Å average pore diameter, was used in the present work. It was previously heated at 150 ºC under vacuum (10^–3 torr) for 4 hours. About 50 g of the activated silica was immersed in dry xylene (100 mL) and 3-Chloropropyltrimethoxysilane (20 mL) was added and the mixture was boiled under reflux, with stirring, under nitrogen atmosphere, for 24 hours. The resulting 3-chloropropyl silica gel was filtered off under nitrogen atmosphere, washed with xylene, EtOH and Et₂O. The product final was denoted by ClPS.

2.2.2. Reaction of 3-chloropropylsilica gel whit DAB-Am-16

The reaction of 3-Chloropropylsilica gel whit DAB-Am-16 was carried out as described in the literature²⁰. In a typical functionalization step, 5 g of 3-chloropropyl silica gel, previously degassed under vacuum (10^–3 torr) at room temperature, was immersed in methanol (25 mL) and 0.01 mol DAB-Am-16 was added. The mixture was stirred 48 hours at 110 ºC. The resulting product, 3-[DAB-Am-16] propyl silica gel, was filtered off, washed with methanol and finally, washed exhaustively with ethanol until a negative test for chloride using AgNO₃. The product was heated at 80 ºC under vacuum (10^–3 torr) for 8 hours. The final solid material was denoted of DPPIPS. The amount of DAB-Am-16 on the silica surface was determined by analyzing the amount of nitrogen with the microanalysis method. Figure 1 shows a scheme for the synthesis of DPPIPS.

2.2.3. Reaction of DPPIPS with copper ions

1.0 g of the modified silica (DPPIPS) was immersed in 25 mL of an aqueous solution of 1.0 × 10^–3 mol.L^–1 of copper ions. This mixture was stirred for 30 minutes at room temperature, and then the solid phase was filtered and washed with bidistilled water. The composite formed was described by CuDPPIPS.

2.3. Isotherms of adsorption

The isotherms of adsorption for CuCl₂ from acetone, ethanol, ethanol 42% and aqueous solutions on the DPPIPS determined by using the batchwise technique. For each isotherm a series of samples containing 0.060 g of the adsorbent in 50.0 mL solvent with variable concentrations of copper ions halide (0.25 × 10^–3 to 3.0 × 10^–3 mol.L^–1) was mechanically shaken for 40 minutes, at a constant temperature of 25 ± 1 ºC. The concentration of the metal ion in solution, in equilibrium with solid phase, was determined by Flame absorption spectrometry (FAAS). The quantity of adsorbed metal, Nf, in each flask was determined by the equation Nf = (Na – Ns)/m, where m is the mass of the adsorbent and Na and Ns are the initial and the equilibrium amount of the number of moles of the metal in the solution phase, respectively.

2.4. Application of DPPIPS for copper determination in ethanol fuel and beverages

Application of DPPIPS for preconcentration and recovery of the copper was carried out using a 15 cm^–1 length and 0.6 cm inner diameter glass tube equipped with a double way valve packed with DPPIPS. About 100 mL of real samples of ethanol fuel and different beverages (sugar cane spirit (or "cachaça"), vodka (38%), ginger brandy), were percolated through the column packed with 2 g of DPPIPS and up rated by a peristaltic pump. Adsorbed metal ions were eluted with 3 mL of 1.0 mol.L^–1 HCl solution and the copper ions analyzed by Flame Absorption Atomic Spectroscopy (FAAS).

2.5. Techniques

2.5.1. Fourier transform infrared spectra (FTIR)

Fourier transform infrared spectra (FTIR) were recorded on a Nicolet 5DXB FT-IR 300 spectrometer. Approximately 600 mg of KBr was ground using a mortar and pestle, and a sufficient amount of solid (about 60 mg) sample was ground with KBr to make a 1 wt. (%) mixture to produce KBr pellets. After the sample was loaded, the sample chamber was purged with nitrogen for a minimum of 10 minutes before data collecting. A minimum of 64 scans was collected for each sample at a resolution of ±4 cm^–1.

2.5.2. Electronic spectra (Uv-Vis)

The electronic spectra were recorded using a Hitachi U-3501 spectrophotometer. The electronic spectra of the immobilized complexes on the silica gel surface were obtained in CCl₄ suspension using a 1 mm path length quartz cell.

2.5.3. Electron paramagnetic resonance analyses

Electron Paramagnetic resonance analyses (EPR) were recorded on a Bruker ESP 300E spectrometer X-band at 25 ºC.

2.5.4. Surface area and porosity analyses

Nitrogen adsorption-desorption isotherms were recorded at liquid nitrogen temperature and relative pressure interval between 0.001 and 0.998 on the equipment supplied by Micromeritics (ASAP 2010). Samples were evacuated prior to measurements at 200 ºC for 12 hours under vacuum of 10 µPa. Surface areas were calculated following the BET method. The pore size distribution was then determined from mercury intrusion porosimetry using the AUTOPORE III equipment (Micrometrics).

2.5.5. Copper determination by Flame Absorption Atomic Spectroscopy (FAAS)

The concentrations of metal ions gathered from the DPPIPS column were determined by Flame Absorption Atomic Spectroscopy (FAAS) according to the standard guidelines of the manufacturers (Spectrometer:Perkin Elmer Analyst 700), choosing resonance lines for the copper and deuterium-arc lamp background correction. For the calibration, synthetic standard solutions containing 1.0 mol.L^–1 HCl, were used.

2.5.6.

Electrochemical measurements

Cyclic voltammograms were performed using the Microquimica (MQP1-PGST) potentiostat. The three electrode systems used in these studies consisted of a modified working electrode (carbon paste electrode), an Ag/AgCl (KCl 3.0 mol.L^–1) reference electrode, and a platinum wire as the auxiliary electrode. The measurements were carried out at 25 ºC.

3. Results and Discussion

The nitrogen content of the modified silica was 1.45% determined by Kjeldahl Method. This result enabled estimating the number of groups linked per unit of the material. For the DPPIPS, each molecule linked at the surface of the silica has 16 nitrogen atoms in its structure it resulted in 6.47 × 10^–5 moles of nitrogenous groups per gram of functionalized material (1.45 × 10^–2 g/(16 × 14 g.mol ^–1)). The surface effect of reaction of DPPI with ClPS were interpreted through nitrogen adsorption and desorption isotherms, according to the method proposed by Brunauer, Emmett, and Teller (BET), in as much as this method is the most commonly employed for the establishment of the surface area in porous solid materials²¹. Table 1 lists the main surface characteristics of the ClPS and DPPIPS.

Figure 2 illustrates a comparison of the isotherms behaviors of ClPS (a) and DPPIPS in its cavities, respectively. The N₂ adsorption-desorption isotherms obtained for the ClPS before and after the modification have behaved as a type IV adsorption, which posses a distinct hysteresis loop²². ClPS and DPPIPS, isotherms has a similar feature, this is an indicative of that both presents a same pore diameter, but with different distribution. The hysteresis loop is evidenced at relative pressure of 0.45 (P/Po), according to the IUPAC²³.

The characterization of ClPS and DPPIPS was first studied using FTIR spectroscopy (Figure 3a, b respectively). In the region between de 3000-2950 cm^–1 are presents a weak bands at attributed to –CH₂ groups and Si-CH₂^[24]. Both ClPS and DPPIPS presents two bands at 2808 cm^–1 and 2944 cm^–1 attributed to ν _(C-H), but in the DPPIPS these two bands are batocromically shifted 46 and 11 cm^–1 respectively (Figure 3b).

The vibrational spectrum of DPPIPS exhibits some absorption that corresponds to the ClPS. A new absorption at 3250 cm^–1 was attributed to the stretching (ν_CN). The spectral difference between these two compounds is in the region between 1250 cm^–1 and 2250 cm^–1. In this region, the bands of bending-group (NH), δ_(NH2) and CN stretch (ν_(CN)) were clearly identifiable in the spectrum of DPPIPS. These mentioned absorptions are characteristic of an aliphatic amine and are in agreement with one reported in the literature²⁵. Another absorption band was identified for DPPIPS at 1469 cm^–1 and was attributed to the C-H bending²⁵. With these results, the FTIR confirm a well established anchorament of DAB-Am-16 on the 3-chloropropyl silica gel. Cu²⁺ was found to react stronger with DPPIPS surface. Initially our interest in copper determination is that Cu²⁺ is among several transition metals commonly contained in several biological fluids²⁶. Uv-Vis spectrum of DPPIPS and CuDPPIPS are shown in Figure 4.

The electronic spectrum in the UV-Vis is quite sensitive to the ligands substitution and the polarity of the solvent²⁴. The CCl₄ was employed as solvent in the studies of electronic spectroscopy using DPPIPS, because CCl₄ presents refraction index η₂₀ = 1,488 next to the one related for silica (η₂₀ = 1,5). The periphery groups of DAB-Am-16 consist of unit called of dipolypropylenetriamine (dpt) (see Figure 1). X-Ray diffraction studies indicate that these groups act as tridentate ligand (see Figure 1). As described in the literature²⁷, the cupric ions in aqueous medium in contact with dendrimer and other ligands is present in the form [Cu(H₂O)₆]²⁺ that in the electronic spectrum give origin to a wide band at 810 nm. An addition of CuCl₂ solution on the DPPIPS in the aqueous or organic medium (methanol) results in the immediately color change (white to blue) ascribed to the d-d band type transitions, suggesting the multiple complexes formation of dpt-Cu on the silica gel surface (CuDPPIPS). In the case of DPPIPS this wide band was observed at λ_máx = 723 nm. As shown Figure 4b, the bathochromic shift (77 nm) was attributed to the matrix effect, because complexes at the higher loading, the number of the metal ions coordinated to the active site dendrimer is not constant, and more than one chemical species is present on the surface, i.e. the Cu(II) can be coordinated to 1 at 8 dpt unit. The electronic spectrums were typical of pentacoordenated specie with square pyramidal structure in concordance with ligand field theory²⁸.

Another characterization was carried out employing voltammetric technique. The voltammograms of CuDPPIPS and DPPIPS were illustrated by Figure 5. The voltammetric spectrum of the CuDPPIPS was not very well defined, as illustrated in Figure 5b. It is clear a presence of anodic peak and a break cathodic peak potential. It is well knowledge which the copper ions are electrochemically inactive in the used potential window and was very interesting to note a presence of redox process. This redox process was attributed at Cu⁰/Cu²⁺ of the complexed copper with dipolypropylenetriamine (dpt) ligand²⁰. The formal potential (E_1/2^ox) (E_1/2^ox = E_pa + E_pc/2 where E_pa and E_pc are anodic and cathodic peak potentials) of CuDPPIPS was of 0.24 V vs SCE (1.0 mol.L^–1 NaCl; pH 6; v = 40 mV.s^–1).

The observed peak to peak separation of CuDPPIPS (ΔEp = E_pa – E_pc) was of 0.23V. An additional break shoulder reduction peak it was observed at 0.21 V, which was attributed to a catalysed Cu²⁺/Cu⁺ process²⁰ due to potential range studied (–0.25 to 1.2 V) the DPPIPS is electroinactive (Figure 5a).

In addition ion Cu²⁺ offers some advantageous features for the application of EPR spectroscopy²⁹. The 3d⁹ configuration (S = 1/2) in its ionized state (Cu²⁺) makes its EPR signal sensitive to ligand substitution. Thus making it possible to obtain information about the structure and the nature of the interaction between dpt-Cu complex on the silica gel.

Copper complexes formed on the silica surface with immobilized dendrimer molecules containing nitrogen have an anisotropic factor (g⊥ of 2.154) as illustrated by Figure 6. In these cases, four nitrogen atoms are in an equatorial plane coordinated to the copper ion. These evidences showed that the DAB-Am-16 groups were bonded on the surface of the silica and cupric ions are coordinated as Lewis acid. It was curiously to verify an absence of hyperfine interactions.

The isotherms of adsorption for Cu(II) from solutions on the DPPIPS materials were determined by using the batchwise technique. Preliminary tests showed that the systems achieve the equilibrium condition at 30 and 40 minutes for DPPIPS. Then, the mixtures was shaken 40 minutes, for DPPIPS, and the concentrations of the metal ions in solution, in equilibrium with solid phase, were determined by flame absorption atomic spectrometry (FAAS). To verify the usefulness of the present grafted dendrimer for adsorption of Cu (II) from aqueous and others solutions, such as water/ethanol (42%), ethanol and acetone, adsorption isotherms were determined. Plotting Nf against C, where C is the equilibrium concentration of the solute in solution phase, the adsorption isotherms for copper ions from different solvents onto DPPIPS surface, are illustrated in Figure 7. An ethanol solutions (42%) was tested due it possibility of copper determination in Brazilian beverage (distilled spirits).The same procedure was applied to untreated silica (3- chloropropylsilica gel), for each cation solution, and did not indicated any adsorption. The adsorption properties decreased in the following sequence: Acetone > ethanol > ethanol/water mixture (42%) > water.

Additional tests showed that the sorption efficiency depends on the solution pH. The quantity of adsorbed metal strongly decreases with the acidity, this is expected, because at low pH NH₂ group is protonated. The optimum acidity conditions for the sorption of metals were in the range of pH 6.5-7.1.

The DAB-Am-16 species grafted on the solid surface behaves as a Lewis base ligand and, probably, Cu²⁺ diffuses from the solution phase into the solid surface as a neutral species. The adsorption of copper ion from these solvents as anionic complexes was much higher from acetone than ethanol solution. In acetone solutions strong copper adsorption was observed on modified silica dendrimer, compared with other solutions tested. Various studies have shown that adsorption in acetone solutions is larger because of great polarity of ethanol which solvates the complexing agent, thus avoiding surface complexation of copper ions on the modified silica. Therefore this behavior is due a physicochemical change of the material properties surface due to a different polarity.

The cupric ions are coordinated to the nitrogen atoms of the DAB-Am-16 groups and the anions can be in the inner coordination sphere, bonded to the metal ion or remaining in the outer sphere, balancing the charge. In any case, the metal adsorption process on the surface with the electrically neutral grafted ligands can be represented by the following complex formation equilibrium³⁰, described by Equation 1.

Assuming that they can be described by the Langmuir equation^31,32 as described by Equation 2:

The adsorption capacity N_s and the equilibrium constant, k were calculated by plotting C/Nf against C for DPPIPS, according to Figure 8. The calculated constants N_s and k are presented in Table 2 together with the linear correlation coefficients r. The results show that there is a good fit between the experimental data and empirical Langmuir isotherm. Table 2 shows the maximum-adsorption data for Cu²⁺ ions on the modified surface of silica dendrimer, in water, water/ethanol 42%, ethanol and acetone solvents. The calculated values of k suggest that the sorption of these metals from solution by the solid phase occurs mainly by surface complexation through nitrogen-to-metal bond formation.

The calculated equilibrium constants for CuCl₂ are nearly the same magnitude demonstrating that the surface complexes are thermodynamically stable^33,34.

The DPPIPS presents some additional advantages for adsorption of the metal ions, such as a high degree of organofunctionalization, great stability, reutilization possibility and high mechanical resistance. Then, this graphited nanostructured material can be potentially useful for analytical purposes, such as for separation and determination of the metal ions from aqueous solutions. The DPPIPS matrix can be used, without any significant loss of adsorption capacity, for various adsorption and desorption operations.

The Table 3 shows the results of the recovery column performed with a solution of 3.728 mg.L^–1 Cu²⁺ in a column packed with DPPIPS, passing 30 mL of different concentrations of HCl. It can be observed that all the metal was eluted with hydrochloric acid 1.00 mol.L^–1 with a percentage of recovery around within the experimental error 100%, but in presence of Ni²⁺ ions this value decreased to 72.6 %. (Table 3). Previous studies have allowed estimating the preconcentration factor (F_pc). The preconcentration factor was calculated using the Equation 3 and had a value of 4.35. Practically every metal ion (99.8%) was eluted with HCl 1.00 mol.L^–1.

The recovery experiment for copper ion from a synthetic solution served as basis for a rapid method for preconcentration and determination of metal ions in different real samples.

As applications of DPPIPS, samples of distilled spirits and fuel alcohol were leached in columns in order to demonstrate the ability of separation of Cu²⁺ ions. After contacting the samples were eluted with 3.0 mL of HCl 1.00 mol.L^–1, collected and completed in a volumetric flask and the concentration of copper was determined by flame atomic absorption spectroscopy, the results the column packed with DPPIPS are represented by Table 4. For the sample of ginger brandy, it was observed a low recovery (93%), probably due to an interaction of secondary organic products present in the sample with the matrix. Through preliminary chromatographic analysis this interaction was observed due to difference in chromatographic (HPLC) profile observed before and after the percolation of the sample in the column containing DPPIPS (results not shown)

To a regeneration of column it is necessary a previous neutralization with KOH (0.5 mol.L^–1) because the adsorbent material was resistant to the attack of concentrated acids, but not to the attack of concentrated aqueous alkali solution.

The main advantage to using the DAB-Am-16 is that dendrimer ligand is biocompatible, non-toxic and have reduced or low toxicity^35-37 different of other ligand highly toxic such as thiadiazole and mercaptopyridine analogues commonly used as ligand for metal adsorption^32,33,38-40 on the silica gel surface. This is an important fact because it opens a good perspective to use this material in the removal of metals in food samples, contaminated liquids such as juices, milk and water. The other important fact is that the dendrimer is not leached from the matrix and its capacities were not affected after several retention/elution cycles during 9 months of continuous use providing an excellent lifetime useful for the material.

4. Conclusions

The functionalization of 3-chloropropyl silica gel (SG) with the dendrimer Hexadecaamine Poly(propylene imine) (DAB-Am-16) was successfully carried out. The studies of FTIR, Reflectance diffuse, and Electron Paramagnetic Resonance (EPR) in the solid state together with cyclic voltammetry confirm the modification of the silica with the (DAB-Am-16) dendrimer. In this study it was observed, by several techniques that Cu²⁺ is adsorbed by surface amino groups.

The composite (DPPIPS) obtained, proved to be very promising in its use in sorption and preconcentration of Cu²⁺ in several solvents and different samples. The Langmuir model allowed to describe the sorption of the metal ions on DPPIPS The high values of the constant (K) in the order of 10³ L.mol ^–1 suggests that the formed complexes on the DPPIPS surface are thermodynamically stable. The sorption–desorption of the metal ions made possible the development of a method for preconcentration and determination of metal ions at trace level in real samples such as commercial ethanol, used as fuel for car engines and also of metals in food samples, contaminated liquids such as juices, milk, water. In particular, a modification of dendrimer on inert substrates could offer an attractive method because they possess a large number of end groups per molecule and may to constitute an excellent candidate for analytical applications.

Acknowledgements

The authors acknowledge financial support from the Fundação de Amparo à Pesquisa do Estado de São Paulo – FAPESP (Proc. 03/12882-6 and 2004/09326-7) and Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq.

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Received: May 4, 2012

Revised: August 23, 2012

Publication Dates

• Publication in this collection
  22 Nov 2012
• Date of issue
  Feb 2013

History

• Received
  04 May 2012
• Accepted
  23 Aug 2012