Cold vapor atomic absorption spectrometric determination of cadmium after solid phase extraction on modified TiO2 nanoparticles

ARTICLE

Cold vapor atomic absorption spectrometric determination of cadmium after solid phase extraction on modified TiO₂ nanoparticles

Reza Hafezi Moghaddam; Ali Mohammad Haji Shabani; Shayessteh Dadfarnia^*; Neda Baghban

Department of Chemistry, Yazd University, 89195-741 Yazd, Iran

ABSTRACT

Cadmium was quantitatively adsorbed from aqueous sample onto a microcolumn packed with cadion immobilized on sodium dodecyl sulfate-coated TiO₂ nanoparticles. The retained cadmium was eluted with 2.5 mol L^-1 hydrochloric acid solution and measured by cold vapor atomic absorption spectrometry (CVAAS). The influences of different variables such as pH, sample and eluent flow rates, amount of the sorbent and volume of the sample on the recovery of cadmium were investigated. Under the optimum conditions, a sample volume of 200 mL resulted in a preconcentration factor of 100. The precision (RSD%, n = 8) at the 0.05 µg L^-1 level of cadmium was 3.6% and the limit of detection based on three times the standard deviation of blank solution (3S_b) was 1.3 ng L^-1. The method was successfully applied to the determination of cadmium in rice, fish, milk, and water samples.

Keywords: cadmium, solid phase extraction, cold vapor atomic absorption spectrometry, cadion, modified TiO₂ nanoparticles

RESUMO

O cádmio de uma amostra aquosa foi quantitativamente adsorvido em uma microcoluna empacotada com cadion imobilizado em nanopartículas de TiO₂ recobertas por dodecilsulfato de sódio. O cádmio retido foi eluido com uma solução de ácido clorídrico 2,5 mol L^-1 e medido por espectroscopia de absorção atômica com vapor frio (CVAAS). As influências de diferentes variáveis, como pH, taxas de fluxo da amostra e do eluente, quantidade do sorvente e volume da amostra, na recuperação do cádmio foram investigadas. Sob condições ótimas, um volume de 200 mL de amostra resultou em um fator de pré-concentração de 100. A precisão (RSD%, n = 8) em 0,05 µg L^-1 de cádmio foi 3,6% e o limite de detecção, baseado em três vezes o desvio padrão do branco (3S_b), foi de 1,3 ng L^-1. O método foi aplicado com sucesso à determinacão de cádmio em amostras de arroz, peixe, leite e água.

Introduction

Cadmium is a highly toxic non-essential element for animals, plants and humans even at low concentrations and can be accumulated in kidneys, liver and lungs.¹ Cadmium is found in phosphate fertilizers, industrial dusts, tobacco smoke, food and some water supplies. The International Agency for Research on Cancer (IARC) classified cadmium as a human carcinogen.² The World Health Organization (WHO) has set a maximum permissible level of 3.0 µg L^-1 for this element in drinking water.³ Therefore, determination of trace or ultra-trace amounts of Cd in water and food samples is of special interest.

The determination of cadmium at trace levels have been performed using a variety of instrumental analytical techniques such as flame atomic absorption spectrometry (FAAS),⁴ electrothermal atomic absorption spectrometry (ETAAS),⁵ inductively coupled plasma optical emission spectrometry (ICP-OES),⁶ spectrofluorimetry,⁷ neutron activation analysis (NAA),⁸ and differential pulse anodic stripping voltammetry (DPASV).^9,10 In recent years, cold vapor generation of cadmium for atomic absorption spectrometry as an alternative sample introduction technique has attracted more attention.^11-13 The main advantages of this technique are: simplicity, rapidity, high sensitivity and relative freedom from interferences. Although cold vapor atomic absorption spectrometry (CVAAS) is a powerful technique for the determination of cadmium at trace levels, a separation and preconcentration step usually is required due to the very low concentration of this element in the environmental samples.

Several procedures for the separation and preconcentration of cadmium from aqueous samples have been developed, including solid phase extraction (SPE),^14,15 coprecipitation,¹⁶ cloud point extraction (CPE),^17,18 liquid-liquid extraction (LLE),¹⁹ temperature-controlled ionic liquid dispersive liquid-phase microextraction (TCIL-DLPME),²⁰ and ultrasound-assisted emulsification solidified floating organic drop microextraction (USAE-SFODME).²¹ Among these separation and preconcentration methods, solid phase extraction has become increasingly more popular because of its advantages of simplicity, rapidity, ease of automation, low cost, low consumption of organic solvents, high recovery and high preconcentration factor. Different substances such as microcrystalline naphthalene,²² XAD resins,²³ modified alumina,²⁴ activated carbon²⁵, titanium dioxide,²⁶ and polyurethane foam²⁷ have been proposed as solid phase extractants. In recent years, a variety of metal oxide nanoparticles (NPs) such as Al₂O₃,²⁸ Fe₃O₄,²⁹ CeO₂,³⁰ ZrO₂³¹ and TiO₂³² have been used as the new solid phase materials for the extraction of metal ions from aqueous samples. Metal oxide nanoparticles have an excellent adsorption capacity toward metal ions owing to their high reactivity, small size and large surface area.³³ Chemical or physical modification of NP surface with appropriate chelating ligand can improve its affinity and selectivity towards metal ions.^34,35

1-(4-nitrophenyl)-3-(4-phenylazophenyl)triazene (cadion), which forms a red water-insoluble chelate with cadmium (Figure 1), is a highly sensitive reagent commonly used for its spectrophotometric determination.³⁶ In this work, the use of cadion immobilized on surfactant-coated TiO₂ NPs for the solid phase extraction of trace amounts of cadmium from aqueous solutions prior to its determination by cold vapor atomic absorption spectrometry is reported.

Experimental

Apparatus

An Analytik Jena model novAA^® 300 (Jena, Germany) atomic absorption spectrometer with deuterium lamp background correction was used for all absorption measurements. A cadmium hollow cathode lamp (Analytik Jena, Germany) operated at 3.0 mA was used as the radiation source. The wavelength and spectral band pass were set at 228.8 and 1.2 nm, respectively.

An Analytik Jena hydride generator (model HS-60, Jena, Germany) was used to produce the cadmium vapor. The vapor generator was used in batch mode. The cadmium ions were reduced to metallic cadmium with sodium tetrahydroborate and argon was used as the carrier gas. Important parameters for cold vapor atomic absorption spectrometric determination of cadmium were investigated and optimized. All the measurements were carried out in the optimized conditions given in Table 1.

The pH measurement was done by a Metrohm pH meter (model 691, Herisau, Switzerland) equipped with a combined glass-calomel electrode. The sample and eluent flow rates through the microcolumn were adjusted using a peristaltic pump (EYELA SMP-23, Tokyo, Japan).

Reagents

TiO₂ nanoparticles (99.5% purity) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Other chemicals were of the highest purity available from Merck (Darmstadt, Germany) and used as received. Double-distilled deionized water was used to prepare all the solutions. A stock solution of Cd(II) at a concentration of 1000 mg L^-1 was prepared by dissolving appropriate amount of Cd(NO₃)₂.4H₂O in 1% (v/v) nitric acid solution. Working solutions were prepared daily by serial dilution of the stock solution. A 1.0% (m/v) sodium tetrahydroborate solution was prepared daily by dissolving an appropriate amount of NaBH₄ in 0.3% (m/v) sodium hydroxide. A 0.04% (m/v) cadion solution was prepared by dissolving 0.04 g of cadion in 100 mL of ethanol. The glassware used was soaked overnight in 10% nitric acid solution and was subsequently rinsed with double-distilled deionized water.

Preparation of the sorbent

TiO₂ NPs were suspended in 25 mL of a solution containing 100 mg of sodium dodecyl sulfate (SDS) and mixed with a magnetic stirrer. Then, 25 mL of cadion solution (0.04% m/v) were added and the pH was adjusted to approximately 2.5 with 1 mol L^-1 hydrochloric acid solution and mixed for 20 min. The mixture was filtered through Millipore filter using a vacuum pump. The solid phase was washed twice with distilled water, air dried and kept in a closed brown bottle for subsequent use. The modified sorbent was stable at least for 2 months.

Preparation of the microcolumn

The microcolumn was made of polytetrafluoroethylene (PTFE, Teflon®) tubing (35 mm in length × 3.0 mm i.d.) filled with a homogeneous mixture of 60 mg cadion-modified TiO₂ NPs and 60 mg of glass beads, which were retained in the column by a small portion of glass wool at both ends of the column. Glass beads were added to cadion-modified TiO₂ NPs to prevent them from packing the column too tight and improve the flow rate and backpressure in the system.³⁵

Recommended procedure

The pH of sample or standard solution containing 1-36 ng of cadmium was adjusted to about 8.0 with diluted sodium hydroxide or hydrochloric acid solution and was passed through the microcolumn at a flow rate of 5 mL min^-1 with the help of a peristaltic pump. The retained cadmium on the microcolumn was then eluted using 2 mL of 2.5 mol L^-1 HCl at a flow rate of 2 mL min^-1 and was transferred to the reduction cell. Five milliliters of 1% (m/v) NaBH₄ solution as the reducing agent were added through the peristaltic pump (Figure 2). The produced cadmium vapor was then directed to the quartz cell by a stream of argon at 160 mL min^-1 and was quantified by atomic absorption spectrometry. All measurements were performed by integrated absorbance mode (peak area).

Sample preparation

Water samples were filtered through a Millipore filter (0.45 µm pore size); the pH of the samples was adjusted to 8.0 with diluted sodium hydroxide or hydrochloric acid solution, and was treated according to the recommended procedure.

Fish muscle samples were oven dried at 40 ºC for about 2 h and 500 mg of dried sample was refluxed with 20 mL of nitric acid (65%) at 200 ºC for 2 h. Then, 10 mL of K₂S₂O₈ (5% m/v) was added and the solution was heated for one hour. After complete digestion, it was cooled, filtered, neutralized with sodium hydroxide solution and diluted to 200 mL with deionized water.³⁷ Fifty milliliters of this solution were analyzed according to the recommended procedure.

Milk samples were analyzed according to the given procedure;^38,39 thus, 5 mL of cow milk were treated with 5 mL concentrated nitric acid and 2 mL of 30% hydrogen peroxide and digested on a hot plate at 90 ºC. Then the temperature of mixture was gradually increased to 120 ºC until brown fumes appeared and the organic matrix of milk was oxidized. After cooling, the solution was filtered and the pH was adjusted to approximately 8. The solution was then transferred to a 50 mL flask and diluted to the mark with distilled water. The final solution was treated according to the recommended procedure.

Rice samples were digested according to the given procedure in the literature,⁴⁰ i.e., the samples were washed thoroughly with distilled water, grounded and dried. An amount of 0.5 g of the rice sample was weighed and added to a beaker; 10 mL of concentrated HNO₃ were added and the mixture was kept overnight. Then, 2 mL of concentrated HClO₄ were added and the solution was evaporated to near dryness on a heater-stirrer at 130 ºC for about 3 h. The clear solution was neutralized and diluted to 200 mL with distilled water. The pH was adjusted to 8 by the addition of diluted sodium hydroxide solution and was treated according to the recommended procedure.

Results and discussion

Modification of TiO₂ nanoparticles with SDS-cadion

Above the so-called critical micellar concentration (CMC), surfactants aggregate and form micelles in aqueous solutions. The hydrophilic ends of the surfactant molecules are in contact with the solvent and the hydrophobic tails are in the center of spherical nanostructure of micelles. However, when the concentrations of surfactants are slightly below the CMC, ionic surfactant molecules can be adsorbed on the active solid surfaces such as alumina, silica, iron oxides and titania exposed to the solution, forming one layer (hemi-micelles) and two layer (ad-micelles) aggregates on these surfaces. Then, hydrophobic compounds can be sorbed into the hydrocarbon cores of these micellar surface aggregates.

The sorption of SDS on TiO₂ nanoparticles was found to be highly dependent on the pH of solution. TiO₂ NPs can strongly adsorb negatively charged SDS surfactant ions at pH below 6 (the isoelectric point of TiO₂ NPs) due to columbic attraction. Thus, when TiO₂ NPs were shaken with acidified solution containing cadion and SDS, the ligand was trapped homogeneously on the hemi-micelles or ad-micelles formed by SDS on TiO₂ NPs and the color changed from white to yellow. The modified sorbent was then characterized by Fourier transform infrared spectroscopy (FTIR). The IR spectra of TiO₂ NPs, pure cadion and cadion immobilized on sodium dodecyl sulfate-coated TiO₂ NPs were recorded using KBr pellets (Figure 3). Comparison of the IR spectra of bare TiO₂ NPs, cadion and modified TiO₂ NPs indicated that modified TiO₂ NPs contain the peaks corresponding to TiO₂ NPs and some bands of the cadion (3272 cm^-1 of N–H stretching, 1595 cm^-1 of N=N, 1478 and 1508 cm^-1 of C=C stretching of aromatic rings, and 1109, 1170 and 1250 cm^-1 of N–C stretching). Some IR bands of SDS (1210 cm^-1 of S=O asymmetric stretching, 1148 cm^-1 of S=O symmetric stretching and 2918 cm^-1 of aliphatic C–H stretching) are also observed in modified TiO₂ NPs spectrum. Thus, it was shown that cadion was successfully immobilized onto the surfaces of the SDS-coated TiO₂ NPs.

Figure 4 portrays the scanning electron spectroscopy (SEM) images of the naked TiO₂ NPs and cadion immobilized on the sodium dodecyl sulfate-coated TiO₂ NPs. According to SEM images, although the average size of cadion immobilized on sodium dodecyl sulfate-coated TiO₂ NPs is increased, it is still in the nano range (about 75 nm).

Effect of variables on sorption and elution of cadmium ions

In order to establish the best conditions for sorption and desorption of cadmium, the influence of various variables such as pH, type, concentration and volume of eluent, sample and eluent flow rates, sample volume, and amount of adsorbent was studied and optimized.

Effect of pH

The reaction between cadmium ions and cadion reagent may be influenced by the pH of the sample solution. Therefore, the effect of the pH on the extraction efficiency of 10 ng Cd from 50 mL of solution was studied by varying the pH of solution in the range of 2.0-12.0. The pH was adjusted by adding either diluted hydrochloric acid or sodium hydroxide solution. As shown in Figure 5, the highest recoveries of Cd were obtained in the pH range 7.0-10.0. At pH greater than 10, recoveries of cadmium extremely decreased probably due to precipitation of cadmium as cadmium hydroxide. On the other hand, the gradual decrease in the recovery of analyte at pH lower than 7 is due to the competition between the proton and cadmium ions for the reaction with the ligand. Therefore, pH 8 was selected for the subsequent studies.

Effect of elution parameters

To ensure the quantitative elution of the cadmium ions from the modified TiO₂ NPs, the type, volume and concentration of the eluent were studied. Two milliliters of different eluents (3 mol L^-1) such as hydrochloric acid, nitric acid, acetic acid and ammonia solution were examined. The results revealed that hydrochloric acid was more effective than the others. The effect of hydrochloric acid concentration was then studied in the range of 0.5 to 3.0 mol L^-1. As shown in Figure 6, the recovery of the analyte increased with an increase in the hydrochloric acid concentration up to 2.5 mol L^-1 and then remained constant at higher concentration. Therefore, subsequent experiments were performed with hydrochloric acid at concentration of 2.5 mol L^-1. The influence of the eluent volume on the desorption of cadmium was also investigated in the range of 0.5-3.0 mL. The results showed that at a volume higher than 2 mL, the recovery of analyte was quantitative. Therefore, a volume of 2 mL was selected as the optimum volume of the eluent in further studies.

Effect of sample and eluent flow rates

The effect of the sample and eluent flow rates on the retention and elution of cadmium ions was also studied. The effect of sample flow rate, in the range of 2.0-9.0 mL min^-1 was investigated by passing 50.0 mL of sample solution containing 20 ng of cadmium through the microcolumn with a peristaltic pump. The results showed that the retention of cadmium is relatively fast and independent of flow rate up to 5.0 mL min^-1. Therefore, a sample flow rate of 5.0 mL min^-1 was selected for subsequent studies.

The effect of the eluent flow rate on the desorption of cadmium from the microcolumn was also studied in the range of 2.0-7.0 mL min^-1 and it was found that the recovery remained constant at the flow rates up to 3.0 mL min^-1. Thus, a flow rate of 3.0 mL min^-1 was selected for the eluent.

Effect of sample volume

To attain the maximum preconcentration factor, the influence of the sample volume on the recovery of cadmium was studied. An aliquot of 50-400 mL of aqueous solution containing 10 ng of cadmium was passed through the microcolumn under the optimum conditions. The recoveries were found to be quantitative and constant up to 250 mL (Figure 7). Therefore, the breakthrough volume for the method is 250 mL and a maximum preconcentration factor of 125 can be obtained based on consideration of the final eluent volume (2 mL) and the breakthrough volume (250 mL).

Effect of the amount of adsorbent

The amount of adsorbent is an important parameter affecting quantitative recovery. In order to estimate the optimum amount of sorbent, the recoveries of cadmium were investigated by varying the amounts of the modified sorbent from 10.0 to 120.0 mg. The results indicated that the quantitative recoveries of Cd were achieved when the amount of sorbent was greater than 60.0 mg. Therefore, 60 mg of the modified TiO₂ NPs were used in subsequent studies.

Sorbent capacity

The maximum sorption capacity of cadion immobilized on SDS-coated TiO₂ NPs was examined in a batch experiment. One hundred milligrams of the sorbent were added to 50 mL of the solution containing 0.3 mg of Cd at pH 8 and the mixture was shaken for 30 min. It should be noted that the sorption of analyte to the sorbent increased with time up to 15 min and then levelled off, thus, in order to guarantee the achievement of equilibrium the mixture was shaken for 30 min. After centrifugation of the mixture, the amount of cadmium left in the solution was determined by flame atomic absorption spectrometry. The maximum sorption capacity of the modified TiO₂ NPs was calculated by the difference between the initial and final concentrations of analyte in the solution and was found to be 1590 ± 42 µg g^-1. This high capacity suggested high performance of the microcolumn even in the presence of competing cations.

Interference studies

The interference of common coexisting metal cations and anions on the solid phase extraction and determination of cadmium was investigated under the optimized conditions. For this purpose, 50 mL of solution containing 10 ng of cadmium and various amounts of coexisting ions were analyzed according to the recommended procedure. A relative error of less than 5% in the determination of cadmium was considered to be within the range of experimental error. As shown in Table 2, even at the presence of high concentration of foreign ions, the cadmium ions in binary mixtures were quantitatively retained on the modified TiO₂ NPs. Thus, the proposed method is selective for the determination of the analyte.

Analytical performance

Under the optimum conditions, for a sample volume of 200 mL, the calibration graph exhibited linearity over the range of 0.005-0.180 µg L^-1 of cadmium. The equation of the calibration graph was A = 2.7771C + 0.0245 (where A is the absorbance and C is the concentration of cadmium in µg L^-1) with a correlation coefficient (r²) of 0.9990. The limit of detection (LOD), defined as 3S_b / m (where S_b is standard deviation of 5 replicate measurements of the blank and m is the slope of the calibration graph) was 1.3 ng L^-1. The precision of the method was evaluated by passing 200 mL of solution containing cadmium through the microcolumn and repeating this procedure eight times. The relative standard deviation (RSD%) for eight replicate measurements of 50 ng L^-1 cadmium was 3.6%. The enhancement factor of 98.1 was obtained from the ratio between the slopes of the calibration graphs constructed with the preconcentrated samples and the ones not submitted to the preconcentration step. The closeness of the enhancement factor (98.1) to the preconcentration factor (100) further indicates the quantitative retention and elution of analyte by the sorbent. A single microcolumn was used up to 9 times in different days without a significant loss in its performance.

Application

The proposed method was applied to the determination of cadmium in well water, river water (taken from Karoon River) and seawater (taken from the Persian Gulf), cow milk, fish and rice samples. In order to validate the method, the recovery experiments were carried out by spiking the samples with a known amount of cadmium before treatment. The results are summarized in Tables 3 and 4. The recoveries are in the range of 95.0-98.8%, and indicate the applicability of the method for the determination of cadmium in different real samples. Furthermore, the accuracy of milk analysis was checked by independent analysis using electrothermal atomic absorption spectrometry. The results were found to be 473 ± 10 and 560 ± 12 for low fat and high fat milk, respectively, which is in agreement with the results obtained by the given procedure.

Comparison with other SPE methods

The figures of merit of the presented method were compared with some of the previously reported solid phase extraction methods for the separation and determination of cadmium and the results are shown in Table 5. As it can be seen, the preconcentration factor (PF) of the proposed method is larger than the other CVAAS techniques and the detection limit is better than the other SPE methods.

Conclusions

Cadion immobilized on sodium dodecyl sulfate-coated TiO₂ NPs has been successfully applied as a novel sorbent for the separation and preconcentration of ultratrace levels of cadmium prior to its determination by cold vapor atomic absorption spectrometry. The method is simple, convenient, inexpensive and environmentally friendly. The method has good sensitivity, high selectivity and relative high preconcentration factor. The proposed method allows determination of cadmium in different real samples with good accuracy and reproducibility.

Submitted: June 1, 2014

Published online: August 1, 2014

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Publication Dates

• Publication in this collection
  13 Nov 2014
• Date of issue
  Nov 2014

History

• Received
  01 June 2014
• Accepted
  01 Aug 2014