César Ricardo Teixeira Tarley

Solid-phase extraction system for Pb (II) ions enrichment based on multiwall carbon nanotubes coupled on-line to flame atomic absorption spectrometry

The present paper proposes the application of multiwall carbon nanotubes (MWCNTs) as a solid sorbent for lead preconcentration using a flow system coupled to flame atomic absorption spectrometry. The method comprises the preconcentration of Pb (II) ions at a buffered solution (pH 4.7) onto 30mg of MWCNTs previously oxidized with concentrated HNO(3). The elution step is carried out with 1.0molL(-1) HNO(3). The effect of the experimental parameters, including sample pH, sampling flow rate, buffer and eluent concentrations were investigated by means of a 2(4) full factorial design, while for the final optimization a Doehlert design was employed. Under the best experimental conditions the preconcentration system provided detection and quantification limits of 2.6 and 8.6mugL(-1), respectively. A wide linear range varying from 8.6 up to 775mugL(-1) (r>0.999) and the respective precision (relative standard deviation) of 7.7 and 1.4% for the 15 and 200mugL(-1) levels were obtained. The characteristics obtained for the performance of the flow preconcentration system were a preconcentration factor of 44.2, preconcentration efficiency of 11min(-1), consumptive index of 0.45mL and sampling frequency estimated as 14h(-1). Preconcentration studies of Pb (II) ions in the presence of the majority foreign ions tested did not show interference, attesting the good performance of MWCNTs. The accuracy of the method was assessed from analysis of water samples (tap, mineral, physiological serum and synthetic seawater) and common medicinal herbs submitted to the acid decomposition (garlic and Ginkgo Biloba). The satisfactory recovery values obtained without using analyte addition method confirms the feasibility of this method for Pb (II) ions determination in different type of samples.

Highly improved sensitivity of TS-FF-AAS for Cd(II) determination at ng L−1 levels using a simple flow injection minicolumn preconcentration system with multiwall carbon nanotubes

A new method for cadmium determination at ng L−1 levels is described. The method is based on the on-line coupling of a flow preconcentration system using multiwall carbon nanotubes (MWCNT) as sorbent with TS-FF-AAS determination. Cadmium preconcentration was at pH 4.9 onto an MWCNT minicolumn (30 mg) for 2 min at a 5.0 mL min−1 flow rate. The elution step is performed by using 0.5 mol L−1 HNO3 and the cadmium desorbed is directly pumped to a TS-FF-AAS. All experimental parameters that play important roles in system performance were evaluated and optimized by means of fractional factorial designs and response surface methodology. The excellent characteristics of MWCNT as sorbent, mainly owing to its high surface area, make it possible to obtain a preconcentration factor of 51-fold, thus improving the detection and quantification limits in TS-FF-AAS, 11.4 and 38.1 ng L−1, respectively. When the flow preconcentration system, FI-TS-FF-AAS, was compared with FAAS alone, an increase in the sensitivity of 640-fold was obtained. The calibration graph was linear with a correlation coefficient higher than 0.999 from 38.1 to 1250 ng L−1. Repeatability of the measurements (n = 10), assessed as relative standard deviation (RSD), was found to be 6.5 and 2.1% for cadmium concentrations of 100 and 1000 ng L−1, respectively. Important parameters to characterize the flow preconcentration system were also evaluated, the consumption index being 0.196 mL, the concentration efficiency 25.5 min−1 and the sample throughput 20 samples per hour. In order to demonstrate the accuracy of the system, addition and recovery studies in water samples (mineral water, tap water and river water) and cigarette samples were carried out. Moreover, for the same purpose, cadmium was determined in certified biological materials (Bovine Liver and Rye Grass), giving an average result in close agreement with the certified value.

Exploiting micellar environment for simultaneous electrochemical determination of ascorbic acid and dopamine.

A simple and reliable method for simultaneous electrochemical determination of ascorbic acid (AA) and dopamine (DA) is presented in this work. It was based on the use of the cationic surfactant cetylpyridinium chloride (CPC) that enables the separation of the oxidation peaks potential of AA and DA. Cyclic voltammetry (CV) as well as pulse differential voltammetry (PDV) were used in order to verify the voltammetric behaviour in micellar media. In the cationic surfactant CPC, a remarkable electrostatic interaction is established with negatively charged AA, as a consequence, the oxidation peak potential shifted toward less positive potential and the peak current increased. On the other hand, the positively charged DA is repelled from the electrode surface and the oxidation peak potential shifts toward more positive potential in comparison to the bare electrode. Therefore, the common overlapped oxidation peaks of AA and DA can be circumventing by using CPC. Parameter that affects the E(pa) and I(pa) such as CPC concentration and pH were studied. Under optimised conditions, the method presented a linear response to AA and DA in the concentration range from 5 to 75 micromol L(-1) and 10 to 100 micromol L(-1), respectively. The proposed method was successfully applied to the simultaneous determination of AA and DA in dopamine hydrochloride injection (DHI) samples spiked with AA.

Simultaneous determination of zinc, cadmium and lead in environmental water samples by potentiometric stripping analysis (PSA) using multiwalled carbon nanotube electrode

The present paper has focused on the potential application of multiwalled carbon nanotube for the development of a new, simple and highly selective electrochemical method for simultaneous Zn (II), Cd (II) and Pb (II) monitoring in water samples (lake and effluent waters), by using potentiometric stripping analysis (PSA). The electrochemical method is based on simultaneous preconcentration/reduction of metal ions onto a multiwall carbon nanotube electrode at -1.3V (versus Ag/AgCl(sat)) in 0.3 mol L(-1) acetate solution containing 15 mg L(-1) Hg (II) ions during 180s, followed by subsequent chemical stripping. The analytical curve for all analytes covered the linear range varying from 58.4 up to 646.2 microg L(-1) with correlation coefficients higher than 0.981. The limits of detection for Zn (II), Cd (II) and Pb (II) were found to be 28.0, 8.4 and 6.6 microg L(-1), while the relative standard deviation (RSD) at 352 microg L(-1) was 5.6, 7.1 and 5.6% (n=5), respectively. The behavior of the simultaneous determination in the presence of following ions Co (II), Cr (III) and Cu (II) was affected by using the analyte:interferent ratio 1:10. Therefore, by using standard addition method, Zn (II), Cd (II) and Pb (II) ions in lake and effluent water samples were determined after the spiking procedure and the results were successfully compared with those obtained by atomic absorption spectrometry (AAS). The obtained results suggest that the proposed method can be applied as a simple and efficient alternative for the simultaneous monitoring of heavy metals in water samples, according to those established requirements from environmental organizations. In addition, this method demonstrates the powerful application of carbon nanotubes in the field of potentiometric stripping analysis.

Sorbent separation and enrichment method for cobalt ions determination by graphite furnace atomic absorption spectrometry in water and urine samples using multiwall carbon nanotubes

A new cobalt ions pre-concentration method, optimised by fractional factorial design, using multiwall carbon nanotubes (MWCNTs) with further Graphite Furnace Atomic Absorption Spectrometry (GFAAS) quantification is described. The method explores the high chemical and physical stability of MWCNTs for improving the detectability of GFAAS. It is based on off-line pre-concentration of 20.0 mL of sample previously buffered (pH 8.82) on MWCNTs at a flow rate of 10.0 mL min−1. After the pre-concentration procedure, the elution step was carried out with 500 µL of 0.524 mol L−1 HNO3 solution at a flow rate of 2.0 mL min−1. Fractional factorial designs and response surface methodology were employed for optimisation of all chemical parameters involved in the pre-concentration procedure, including pre-concentration flow rate, buffer and eluent concentration, sample pH and elution volume. The method provides a linear calibration range from 0.03 up to 7.00 µg L−1 with linear correlation coefficient higher than 0.9994 and limits of detection and quantification of 0.01 and 0.03 µg L−1, respectively. Repeatability of the six measurements was found to be 2.38 and 1.84% for 0.3 and 4.5 µg L−1 cobalt concentration, respectively. By pre-concentrating 20.0 mL of sample, a pre-concentration factor (PF) of 19.10-fold and a consumption index of 1.05 mL were obtained. The pre-concentration efficiency (PE) was found to be 9.55 min−1. The proposed method was successfully applied for the pre-concentration and determination of cobalt in water and urine samples with satisfactory recovery values.

Synthesis and application of a peroxidase-like molecularly imprinted polymer based on hemin for selective determination of serotonin in blood serum

This work reports the preparation of a molecularly imprinted polymer (MIP) for selective catalytic detection of serotonin (5-hydroxytryptamine, 5-HT). The process is based on the synthesis of polymers with hemin introduced as the catalytic center to mimic the active site of peroxidase. The copolymer MIP, containing artificial recognition sites for 5-HT, has been prepared by bulk polymerization using methacrylic acid (MAA) and hemin as the functional monomers, and ethylene glycol dimethacrylate (EGDMA) as the cross-linker. For the determination of 5-HT, a flow injection analysis system coupled to an amperometric detector was optimized using multivariate analysis. The effects of different parameters, such as pH, buffer flow rate, buffer nature, peroxide concentration and sample volume were evaluated. After optimizing the experimental conditions, a linear response range from 1.0 up to 1000.0 micromolL(-1) was obtained with a sensitivity of 0.4nA/ micromolL(-1). The detection limit was found to be 0.30 micromolL(-1), while the precision values (n=6) evaluated by relative standard deviation (R.S.D.) were, respectively, 1.3 and 1.7% for solutions of 50 and 750 micromolL(-1) of 5-HT. No interference was observed by structurally similar compounds (including epinephrine, dopamine and norepinephrine), thus validating the good performance of the imprinted polymer. The method was applied for the determination of 5-HT in spiked blood serum samples.

Factorial Design and Doehlert Matrix in Optimization of Flow System for Preconcentration of Copper on Polyurethane Foam Loaded with 4‐(2‐Pyridylazo)‐resorcinol

Abstract The present paper describes a flow preconcentration system for copper determination by flame atomic absorption spectrometry (FAAS) based on the sorption of Cu(II) ions onto a mini‐column of polyurethane foam (PUF) loaded with a chromogenic reagent [4‐(2‐pyridylazo)‐resorcinol (PAR)]. The variables associated with flow preconcentration system performance, such as pH, buffer concentration (BC), and sampling flow rate (SF), were optimised using a full factorial (23) design plus a central point and Doehlert matrix. The results obtained, based on the Pareto chart and analysis of variance (ANOVA), demonstrated that pH and BC, as well as the interaction (pH × BC) are statistically significant at the 95% confidence level. By using 20 mL of sampling volume the proposed method, under conditions optimised by the Doehlert matrix (formation of Cu(II)‐PAR (1:2) complex at pH 6.4, 0.017 mol L−1 phosphate BC, and 10 mL min−1 SF), allows to determine Cu(II) ions with a detection limit of 0.35 µg L−1 and precision (n = 8) as relative standard deviation (RSD) of 3.2 and 1.1 for copper solutions containing 10 and 30 µg L−1, respectively. Also, a satisfactory linear range (1.2–40 µg L−1), an enrichment factor of 105 and a sample throughput of 28 hr−1 were achieved. Interference studies showed that the PUF‐PAR mini‐column retains Cu(II) ions in the presence of several transition and alkali metals without presenting interferences. The method was applied for copper determination in water samples (mineral and tap water) and high salt aqueous samples (physiological serum containing 0.9% (m/v) NaCl). The validation of the method was checked by analysing the Cu(II) content in the samples, as well as from analyte addition. The recoveries ranged from 91.0% to 101.1%.

Novel on-line sequential preconcentration system of Cr(III) and Cr(VI) hyphenated with flame atomic absorption spectrometry exploiting sorbents based on chemically modified silica.

In the present study, a flow injection system using dual mini-columns, SiO(2)/Al(2)O(3)/TiO(2) and silica gel functionalized with [3-(2-aminoethylamino)propyl] trimethoxysilane (SiO(2)/AAPTMS) for the sequential preconcentration of Cr(III) and Cr(VI), respectively, from water samples with FAAS detection was proposed. A two-level full factorial design (2(4)) and desirability function were employed for the optimization of variables related to the system performance. The detection limits of 0.66 and 0.27 μg L(-1) for Cr(III) and Cr(IV), respectively, were obtained under the optimized preconcentration conditions (flow rate of 7.0 mL min(-1)), pH 5.0, buffer concentration (acetate buffer) of 0.01 mol L(-1), and eluent (2.5 mol L(-1) HCl) flow rate of 5.0 mL min(-1). The other parameters including preconcentration factor (PF), consumptive index (CI), and concentration efficiency (CE) were found to be 17.62/32.98, 1.13/0.6 mL, and 6.2/11.54 min(-1) for Cr(III)/Cr(VI), respectively. The developed method was applied to the Cr(III) and Cr(VI) determination in water samples [tap, lake and mineral water, artificial saliva and parenteral solutions (physiological serum, water for injection, and glucose physiological solution)]. The method accuracy was checked by the analysis of standard reference materials (trace elements in water).

Amperometric determination of chloroguaiacol at submicromolar levels after on-line preconcentration with molecularly imprinted polymers

In this study, a sorbent flow preconcentration system coupled to amperometric detector for the chloroguaiacol (4-chloro-2-methoxyphenol) determination at submicromolar levels is described. The satisfactory selectivity of the proposed method was attained by means of the use of a chloroguaiacol-imprinted polymer, whose the synthesis was carried out by bulk polymerization. Flow and chemical parameters associated to the preconcentration system, such as sample pH, preconcentration and elution flow rates, concentration of the carrier solution (KCl) and eluent volume were investigated through multivariate analysis. The flow preconcentration of chloroguaiacol was not affect by equimolar presence of structurally similar phenolic compounds including catechol, 4-chloro-3-methylphenol, 4-aminophenol and 2-cresol, thus showing the good performance of the imprinted polymer. Under the best experimental conditions, it was obtained a preconcentration factor of 110-fold and low detection and quantification limits of 27 and 78 nmol L(-1), respectively. The analytical curve covered a wide linear range from 0.05 up to 5.0 micromol L(-1) (r>0.999) and satisfactory precision (n=8) evaluated by relative standard deviation (R.S.D.) were respectively, 5.5 and 4.2%, for solutions of 1.0 and 5.0 micromol L(-1) chloroguaiacol. Other parameters related to the performance of the flow system were also evaluated including concentration efficiency of 27.5 min(-1) and consumptive index of 0.09 mL. Recoveries varying from 93 up to 112% for water samples (tap water and river water) spiked with chloroguaiacol concentration were achieved, thus assuring the accuracy of the proposed flow preconcentration system.

Improved selective cholesterol adsorption by molecularly imprinted poly(methacrylic acid)/silica (PMAA–SiO2) hybrid material synthesized with different molar ratios

The present paper describes the synthesis of molecularly imprinted polymer - poly(methacrylic acid)/silica and reports its performance feasibility with desired adsorption capacity and selectivity for cholesterol extraction. Two imprinted hybrid materials were synthesized at different methacrylic acid (MAA)/tetraethoxysilane (TEOS) molar ratios (6:1 and 1:5) and characterized by FT-IR, TGA, SEM and textural data. Cholesterol adsorption on hybrid materials took place preferably in apolar solvent medium, especially in chloroform. From the kinetic data, the equilibrium time was reached quickly, being 12 and 20 min for the polymers synthesized at MAA/TEOS molar ratio of 6:1 and 1:5, respectively. The pseudo-second-order model provided the best fit for cholesterol adsorption on polymers, confirming the chemical nature of the adsorption process, while the dual-site Langmuir-Freundlich equation presented the best fit to the experimental data, suggesting the existence of two kinds of adsorption sites on both polymers. The maximum adsorption capacities obtained for the polymers synthesized at MAA/TEOS molar ratios of 6:1 and 1:5 were found to be 214.8 and 166.4 mg g(-1), respectively. The results from isotherm data also indicated higher adsorption capacity for both imprinted polymers regarding to corresponding non-imprinted polymers. Nevertheless, taking into account the retention parameters and selectivity of cholesterol in the presence of structurally analogue compounds (5-α-cholestane and 7-dehydrocholesterol), it was observed that the polymer synthesized at the MAA/TEOS molar ratio of 6:1 was much more selective for cholesterol than the one prepared at the ratio of 1:5, thus suggesting that selective binding sites ascribed to the carboxyl group from MAA play a central role in the imprinting effect created on MIP.