A. C. Spinola Costa

Nickel determination in saline matrices by ICP-AES after sorption on Amberlite XAD-2 loaded with PAN.

In the present paper, a solid phase extraction system for separation and preconcentration of nickel (ng g(-1)) in saline matrices is proposed. It is based on the adsorption of nickel(II) ions onto an Amberlite XAD-2 resin loaded with 1-(2-pyridylazo)-2-naphthol (PAN) reagent. Parameters such as the pH effect on the nickel extraction, the effect of flow rate and sample volume on the extraction, the sorption capacity of the loaded resin, the nickel desorption from the resin and the analytical characteristics of the procedure were studied. The results demonstrate that nickel(II) ions, in the concentration range 0.10-275 microg l(-1), and pH 6.0-11.5, contained in a sample volume of 25-250 ml, can be extracted by using 1 g Amberlite XAD-2 resin loaded with PAN reagent. The adsorbed nickel was eluted from the resin by using 5 ml 1 M hydrochloric acid solution. The extractor system has a sorption capacity of 1.87 mumol nickel per g of Amberlite XAD-2 resin loaded with PAN. The precision of the method, evaluated as the R.S.D. obtained after analyzing a series of seven replicates, was 3.9% for nickel in a concentration of 0.20 microg ml(-1). The proposed procedure was used for nickel determination in alkaline salts of analytical grade and table salt, using an inductively coupled plasma atomic emission spectroscopy technique (ICP-AES). The standard addition technique was used and the recoveries obtained revealed that the proposed procedure shows good accuracy.

Copper determination in natural water samples by using FAAS after preconcentration onto amberlite XAD-2 loaded with calmagite.

A procedure for separation and preconcentration of trace amounts of copper in natural water samples, has been proposed. It is based on the adsorption of copper(II) ions onto a column of Amberlite XAD-2 resin loaded with calmagite reagent. This way amounts of copper within the range from 0.0125 to 25.0 microg, in a sample volume of 25 to 250 ml, and pH from 3.7 to 10.0 was concentrated as calmagite complex in a column of 0.50 g of Amberlite XAD-2 resin. Copper (II) ion was desorpted by using 5.0 ml of 2 mol l(-1) hydrochloric acid. Detection and determination limits of the proposed procedure for 250 ml sample volume were 0.15 and 0.50 microg l(-1), respectively. Selectivity test showed that (in the indicated concentration), calcium(II) (500 mg l(-1)), magnesium(II) (500 mg l(-1)), strontium(II) (50 mg l(-1)), iron(III) (10 mg l(-1)), nickel(II) (10 mg l(-1)), cobalt(II) (10 mg l(-1)), cadmium(II) (10 mg l(-1)) and lead(II) (10 mg l(-1)) did not interfere in copper determination by this procedure. Precision of the method, evaluated as the relative standard deviation by analyzing a series of seven replicates, was 2.42% for a copper mass of 1.0 microg in a sample volume of 100 ml. The accuracy of the proposed procedure was evaluated by means of copper determination in reference biological samples. The achieved results were in good agreement with certified values. The extractor system had a sorption capacity of 1.59 mumol of copper per gram of resin loaded with calmagite. The proposed procedure was applied for copper determination by FAAS in natural water samples. Samples were collected from different places of Salvador city, Bahia, Brazil. The achieved recovery, measured by the standard addition technique, showed that the proposed procedure had good accuracy. A good enrichment factor (50x) and simplicity are the main advantages in this analytical procedure.

Derivative spectrophotometric determination of nickel using Br-PADAP

A major problem with spectrophotometric methods for nickel is cobalt interference, because many of the reagents for nickel also react with cobalt. In this work, the interference of cobalt in the determination of nickel using 2-(5-bromo-2-pyridylaxo)-5-diethylaminophenol (Br-PADAP) was eliminated by the use of derivative spectrophotometry, using the zero-crossing method for evaluation of the derivative signal. Br-PADAP reacts with nickel(II) in the presence of Triton X-100 to form a red complex with absorption maxima at 530 and 562 nm. The reactions parameters and the conditions for the measurements of the first-derivative signal were studied and the results demonstrated that using the derivative technique, Br-PADAP can be used for nickel determination with a selectivity higher than that of ordinary spectrophotometry and with a limit of detection of 0.2 ng ml(-1). The pH should be in the range 5.0-6.0 using an acetate buffer. The determination of nickel in the presence of cobalt was performed with conventional and derivative procedures, and the results demonstrated that only the derivative method should be used and, of the methods used for evaluation of the derivative signal, the zero-crossing method is the best. The proposed procedure was used for nickel determination in steels standards. The results demonstrated that the procedure has satisfactory accuracy and precision. Cobalt interference can be also eliminated by using dual-wave-length spectroscopy.

Simultaneous spectrophotometric determination of nickel and iron in copper-base alloy with bromo-PADAP

The reaction of nickel (II) with Br-PADAP, in the presence of tergitol NPX surfactant, forms a complex with absorption peaks at 520 and 560 nm. The iron(II)-Br-PADAP system at the same conditions forms a chelate with absorption peaks at 560 and 748 nm. This allows the simultaneous spectrophotometric determination of nickel and iron by measuring the absorbance at 560 and 748 nm. The proposed method, at ph 4.0-5.7, shows a molar absorptivity of 1.22 x 10(5)l . mole(-1) . cm(-1) for nickel at 560 nm and 8.20 x 10(4)l . mole(-1) . cm(-1) at 560 nm and 3.35 x 10(4)l . mole(-1) . cm(-1) at 748 nm for iron(II). Beers law is obeyed up to 0.40 mu/ml of nickel(II) and up to 0.65 mu/ml of iron(II). Thiosulphate as masking agent allows the simultaneous determination of iron and nickel in the presence of high concentrations of copper. The ethylene glycol 2-(2-amino-ethyl) tetracetic acid provides the elimination of many other interferences. The method has been applied successfully to the simultaneous determination of nickel and iron in reference samples.

Line Selection and Determination of Trace Amounts of Elements in High-Purity Iron by Inductively Coupled Plasma Atomic Emission Spectrometry

Abstract The iron matrix effect on the determination of trace amounts of Zn, Pb, Mn, Cd, Cr, Cu, and Co was studied. An analytical profile of 21 spectral lines of these elements were made, in order to inspect the spectral interference and to study the background in the region of each line using iron solutions of different concentrations. Interference free spectral lines, for some elements, have been recommended to be used for analysis. Recoveries from the iron commercial product spiked with 0.100 μg each of seven analytes are reported. For determination of trace metal a removal of iron by solvent extraction technique prior to the instrumental measurements was required.

Spectrophotometric determination of vanadium(IV) in the presence of vanadium(V) using Br-PADAP

In the present paper, a simple and sensitive method is proposed for vanadium(IV) determination in the presence of vanadium(V). This is based on the oxidation of vanadium(IV) present in the sample to vanadium(V) by addition of iron(III) cation, followed by a complexation reaction of iron(II) with the spectrophotometric reagent 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (Br-PADAP). The iron(II) reacts with Br-PADAP immediately, forming a stable complex with a large molar absorptivity. The vanadium(IV) determination is possible, with a calibration sensitivity of 0.549 μg ml−1, for an analytical curve of 18.8 ng ml−1 to 2.40 μg ml−1, molar absorptivity of 2.80 × 104 1 mole−1 cm−1 and a detection limit of 5.5 ng ml−1. Selectivity was increased with the use of EDTA as a masking agent. The proposed method was applied for the vanadium(IV) determination in the presence of several amounts of vanadium(V). The results revealed that 200 μg of vanadium(V) do not interfere with determination of 5.00 μg of vanadium(IV). The precision and the accuracy obtained were satisfactory (R. S. D.<2%).

Determination of iron in alkaline salts by ICP-AES using 1-(2-Thiazolylazo)-p-cresol (TAC) for preconcentration and separation

The present paper describes the use of 1-(2-thiazolylazo)-p-cresol (TAC) for separation, preconcentration and determination of iron traces (ng g-1) in alkaline salts by the ICP-AES technique. The proposed method is based on the liquid-liquid extraction of the complex formed between iron(III) and 1-(2-thiazolylazo)-p-cresol (TAC). Parameters such as: TAC amount, pH effect, influence of the organic solvent on the extraction, back extraction and mineralization of the organic phase were studied. The results show that the iron(III)-TAC complex, formed in the pH range from 4.0 to 10.0, can be quantitatively extracted from saline solutions (up to 30% NaCl) using isoamyl alcohol, carbon tetrachloride, chloroform or methyl isobutyl ketone as extracting solvent. The solution for the iron determination can be obtained by a back extraction using 1 mol/L hydrochloric acid or 1 mol/L nitric acid solutions or also by mineralization of the organic phase, which was accomplished by evaporation of the organic solvent and digestion of the residue with concentrated nitric acid. The procedure was used for iron determination in several alkaline salt samples. The standard addition technique was applied and the recoveries obtained revealed that the proposed procedure has a good accuracy.

2-(2-Thiazolylazo)-pcresol (TAC) as a reagent for the spectrophotometric determination of titanium (IV)

The reaction between titanium(IV) and 2-(2-thiazolylazo)-p-cresol-(TAC) in aqueous methanol media at apparent pH 4.0–5.6 results in a intensely coloured complex that is stable for at least 2 h. The combining ratio is 1 ∶ 1 cation ∶ TAC. Beers law is obeyed up to 5.0 μg/ml titanium(IV) at 580 nm. The apparent molar absorptivity at 580 nm is 9.82.103 l.mole−1.cm−1 and the detection limit obtained was 5 ng/ml titanium (IV). A spectrophotometric method for the simultaneous determination of titanium and iron with TAC is proposed.

Spectrophotometric and inductively coupled plasma atomic emission spectrometric determination of titanium in ilmenites after rapid dissolution with phosphoric acid

The use of 85% phosphoric acid in borosilicate conical flasks for the dissolution of ilmenites at 230 +/- 10 degrees C is reported. The samples were quantitatively dissolved in less than 13 min. Titanium was determined by both spectrophotometry and inductively coupled plasma atomic emission spectrometry ICP-AES. Vanadium and iron were determined by ICP-AES. In several samples of ilmenites analyzed, the TiO(2) concentration was in the range 10.6-57.5% and those of FeO and V(2)O(5) were in the ranges 31.6-51.4% and 0.39-1.32%, respectively. In the spectrophotometric method, vanadium interference occurs only when the Ti V concentration ratio is <4. In all samples analyzed this ratio was around 12, resulting in no interferences due to vanadium. Hence the ilmenite dissolution procedure using phosphoric acid was compatible with titanium quantification by both spectrophotometry and ICP-AES.

Determination of Nickel in Alkaline Salts by Inductively Coupled Plasma Atomic Emission Spectroscopy Using 1-(2-Thiazolylazo)-p-Cresol for Preconcentration and Separation

Abstract The present paper describes the use of 1-(2-thiazolylazo)-p-cresol (TAC) for separation, preconcentration and determination of nickel (ng g−1) in alkaline salts using Inductively Coupled Plasma Atomic Emission Spectroscopy technique (ICP-AES). The method proposed is based on the liquid-liquid extraction of the complex formed between nickel(II) cation and 1-(2-thiazolylazo)-p-cresol (TAC). Parameters such as: TAC concentration, effect of pH, influence of the organic solvent on the extraction, back extraction and mineralisation of the organic phase were studied. The results demonstrated that nickel in the form of nickel(II)-TAC complex, in the pH range of 5.0 to 12.0, can be quantitatively extracted from saline solutions (up to 30% NaCl) using the following solvents: isoamyl alcohol, carbon tetrachloride, chloroform, xylene, hexane, butyl acetate or methyl isobutyl ketone. The solution for the nickel determination can be obtained by a back extraction using 5 ml of a 1M hydrochloric acid solution or...