Mariana Gava Segatelli

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.

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.

Characterization and use of Moringa oleifera seeds as biosorbent for removing metal ions from aqueous effluents

Moringa oleifera seeds were investigated as a biosorbent for removing metal ions from aqueous effluents. The morphological characteristics as well as the chemical composition of M. oleifera seeds were evaluated using Fourier Transform Infrared (FT-IR) Spectroscopy, Thermogravimetric Analysis (TGA), X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The FT-IR spectra showed the presence of lipids and protein components. Scanning electron micrographs showed that Moringa seeds have an adequate morphological profile for the retention of metal ions. The results suggest that M. oleifera seeds have potential application in Cd(II), Pb(II), Co(II), Cu(II) and Ag(I) decontamination from aqueous effluents.

Grafting 3-mercaptopropyl trimethoxysilane on multi-walled carbon nanotubes surface for improving on-line cadmium(II) preconcentration from water samples.

In the present study, the performance of multi-walled carbon nanotubes (MWCNTs) grafted with 3-mercaptopropyltrimethoxysilane (3-MPTMS), used as a solid phase extractor for Cd(2+) preconcentration in a flow injection system coupled to flame atomic absorption spectrometry (FAAS), was evaluated. The procedure involved the preconcentration of 20.0 mL of Cd(2+) solution at pH 7.5 (0.1 mol L(-1) buffer phosphate) through 70 mg of 3-MPTMS-grafted MWCNTs packed into a minicolumn at 6.0 mL min(-1). The elution step was carried out with 1.0 mol L(-1) HCl. Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were used to estimate the extent of the MWCNT chemical modification. The 3-MPTMS-grafted MWCNTs provided a 1.68 times improvement in the sensitivity of the Cd(2+) FAAS determination compared to the unsilanized oxidized MWCNTs. The following parameters were obtained: preconcentration factor of 31.5, consumptive index of 0.635 mL, sample throughput of 14 h(-1), and concentration efficiency of 9.46 min(-1). The analytical curve was constructed in the range of 1.0-60.0 μg L(-1) (r=0.9988), and the detection and quantification limits were found to be 0.15 μg L(-1) and 0.62 μg L(-1), respectively. Different types of water samples and cigarette sample were successfully analyzed, and the results were compared using electrothermal atomic absorption spectrometry (ETAAS) as reference technique. In addition, the accuracy of proposed method was also checked by analysis of certified reference material NIST SRM 1573a (tomato leaves) and standard reference material NIST SRM 1643e (trace elements in natural waters).

Silica-alumina-niobia (SiO2/Al2O3/Nb2O5) matrix obtained by the sol-gel processing method: new material for online extraction of zinc ions

In the present work, a new material, SiO2/Al2O3/Nb2O5 (designated as SiAlNb), was evaluated as an adsorbent in a flow injection spectrophotometric method for online preconcentration and determination of trace amounts of Zn2+ ions. The preconcentration method is based on Zn2+ adsorption onto the surface of SiAlNb in alkaline medium (pH 9.0). The elution step is carried out using HNO3 solution, followed by reaction of the Zn2+ ions with 1-(2-piridylazo)-2-naphtol (pan) in ammoniacal buffer solution (pH 9.3) containing Tween-80. The [Zn(pan)2] complex formed is determined at 560 nm. The method presented a linear range between 7.6 and 180.0 µg L-1 (r = 0.9992) and limits of detection and quantification of 2.3 and 7.6 µg L-1, respectively. According to the Langmuir linear model, the maximum adsorption capacity was found to be 7.0 mg of Zn2+ g-1 of SiAlNb. The proposed method was successfully applied to the Zn2+ determination in water samples (lake, mineral, tap) and certified reference material (TORT-2 Lobster Hepatopancreas).

Preparation of new ion-selective cross-linked poly(vinylimidazole-co-ethylene glycol dimethacrylate) using a double-imprinting process for the preconcentration of Pb2+ ions

A new ion-selective cross-linked poly(vinylimidazole-co-ethylene glycol dimethacrylate) prepared via a double-imprinting process was developed for the recognition and preconcentration of Pb(2+) from water samples. The sorbent was characterized by FT-IR, SEM, TGA and textural data. The maximum dynamic sorption capacity of Pb(2+) was 42.04 mg Pb(2+) g(-1) of the double-imprinted polymer. The sorption kinetics data were described by a pseudo-second-order model. The double-imprinted polymer exhibited a higher sorption efficiency of Pb(2+) than the blank polymer (non-imprinted polymer). The preconcentration procedure involved the loading of a Pb(2+) solution at pH 7.25 through 40.0 mg of the double-imprinted polymer packed in a mini-column at 5.0 mL min(-1). The selective efficiency of proposed method for the Pb(2+) preconcentration was assured by competitive sorption using different proportions of Pb(2+)/cations and Pb(2+)/anions. An analytical curve was obtained in the range 0.0-300.0 μg L(-1) (r=0.999) and a limit of detection of 2.46 μg L(-1) was obtained. The preconcentration factor was found to be 21, the consumptive index 0.95 mL and the concentration efficiency 5.25 min(-1). The preconcentration method was successfully applied to the Pb(2+) ions determination in different kinds of water samples with high recovery values (91.3-108.9%).

Hybrid molecularly imprinted poly(methacrylic acid-TRIM)-silica chemically modified with (3-glycidyloxypropyl)trimethoxysilane for the extraction of folic acid in aqueous medium

In the present study a hybrid molecularly imprinted poly(methacrylic acid-trimethylolpropane trimethacrylate)-silica (MIP) was synthesized and modified with (3-glycidyloxypropyl)trimethoxysilane (GPTMS) with posterior opening of epoxy ring to provide hydrophilic properties of material in the extraction of folic acid from aqueous medium. The chemical and structural aggregates of hybrid material were characterized by means of Fourier Transform Infrared (FT-IR), Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Thermogravimetric analysis (TGA) and textural data. Selectivity data of MIP were compared to non-imprinted polymer (NIP) through competitive sorption studies in the presence of caffeine, paracetamol or 4-aminobenzamide yielding relative selectivity coefficients (k′) higher than one unit, thus confirming the selective character of MIP even in the presence of structurally smaller compounds than the folic acid. The lower hydrophobic sorption by bovine serum albumin (BSA) in the MIP as compared to unmodified MIP proves the hydrophilicity of polymer surface by using GPTMS with opening ring. Under acid medium(pH 1.5) the sorption of folic acid onto MIP from batch experiments was higher than the one achieved for NIP. Equilibrium sorption of folic acid was reached at 120 min for MIP, NIP and MIP without GPTMS and kinetic sorption data were well described by pseudo-second-order, Elovich and intraparticle diffusion models. Thus, these results indicate the existence of different binding energy sites in the polymers and a complex mechanism consisting of both surface sorption and intraparticle transport of folic acid within the pores of polymers.

Polímeros impressos com íons: fundamentos, estratégias de preparo e aplicações em química analítica

Chemical imprinting technology has been widely used as a valuable tool in selective recognition of a given target analyte (molecule or metal ion), yielding a notable advance in the development of new analytical protocols. Since their discovery, molecularly imprinted polymers (MIPs) have been extensively studied with excellent reviews published. However, studies involving ion imprinted polymers (IIPs), in which metal ions are recognized in the presence of closely related inorganic ions, remain scarce. Thus, this review involved a survey of different synthetic approaches for preparing ion imprinted adsorbents and their application for the development of solid phase extraction methods, metal ion sensors (electrodes and optodes) and selective membranes.