Pedro de Magalhães Padilha

Copper determination in ethanol fuel by differential pulse anodic stripping voltammetry at a solid paraffin-based carbon paste electrode modified with 2-aminothiazole organofunctionalized silica.

Solid paraffin-based carbon paste electrodes modified with 2-aminothiazole organofunctionalized silica have been applied to the anodic stripping determination of copper ions in ethanol fuel samples without any sample treatment. The proposed method comprised four steps: (1) copper ions preconcentration at open circuit potential directly in the ethanol fuel sample; (2) exchange of the solution and immediate cathodic reduction of the absorbate at controlled potential; (3) differential pulse anodic stripping voltammetry; (4) electrochemical surface regeneration by applying a positive potential in acid media. Factors affecting the preconcentration, reduction and stripping steps were investigated and the optimum conditions were employed to develop the analytical procedure. Using a preconcentration time of 20min and reduction time of 120s at -0.3V versus Ag/AgCl(sat) a linear range from 7.5x10(-8) to 2.5x10(-6)mol L(-1) with detection limit of 3.1x10(-8)mol L(-1) was obtained. Interference studies have shown a decrease in the interference effect according to the sequence: Ni>Zn>Cd>Pb>Fe. However, the interference effects of these ions have not forbidden the application of the proposed method. Recovery values between 98.8 and 102.3% were obtained for synthetic samples spiked with known amounts of Cu(2+) and interfering metallic ions. The developed electrode was successfully applied to the determination of Cu(2+) in commercial ethanol fuel samples. The results were compared to those obtained by flame atomic absorption spectroscopy by using the F-test and t-test. Neither F-value nor t-value have exceeded the critical values at 95% confidence level, confirming that there are no significant differences between the results obtained by both methods.

Determination of Metal Ions in Natural Waters by Flame-AAS after Preconcentration on a 5-Amino-1,3,4-Thiadiazole-2-Thiol Modified Silica Gel.

ABSTRACT 5-amino-1,3,4-thiadiazole-2-thiol groups attached on a silica gel surface have been used for adsorption of Cd(II), Co(II), Cu(II), Fe(III), Ni(II), Pb(II) and Zn(II) from aqueous solutions. The adsorption capacities for each metal ion were (in mmol.g−1): Cd(II)= 0.35, Co(II)= 0.10, Cu(II)= 0.15, Fe(III)= 0.20, Hg(II)= 0.46, Ni(II)= 0.16, Pb(II)= 0.13 and Zn(II)= 0.15. The modified silica gel was applied in the preconcentration and quantification of trace level metal ions present in water samples (river, and bog water).

Preconcentration and determination of Cu(II) in a fresh water sample using modified silica gel as a solid-phase extraction adsorbent

A method was developed to attach 4-amino-2-mercaptopyrimidine (AMP) onto silica gel surface and to determine trace metals. The surface functionalization reaction was performed with a silylant agent, chloropropyltrimethoxysilane (Si-CPTS), and the product, Si-AMP, was characterized by FT-IR and elemental analysis to evaluate the surface modification. The functionalized silica was applied in the sorption of Cu(II) ions from an aqueous medium. The series of adsorption isotherms were adjusted to a modified Langmuir equation and the maximum number of moles of adsorbed copper was 0.447 mmol g(-1). The modified material was placed in a preconcentration system, where it reached an approximately 20-fold enrichment factor using 5mg of Si-AMP. The proposed method was applied in the preconcentration and determination of Cu(II) in a fresh water sample from the Paraná river and was validated through a comparative analysis of a standard reference material (1643e).

Determination of Metal Ions in Fuel Ethanol after Preconcentration on 5-Amino-1,3,4-Thiadiazole-2-Thiol Modified Silica Gel

This work describes the synthesis and characterization of 5-amino-1,3,4-thiadiazole-2-thiol modified silica gel (SiATT), and the results of a study of the adsorption and preconcentration (in batch, and in flow using a column technique) of Cd(II), Co(II), Cu(II), Fe(III), Ni(II), Pb(II) and Zn(II) in ethanol medium. The adsorption capacities for each metal ion were (in mmol g-1): Cd(II) = 0.11, Co(II) = 0.10, Cu(II) = 0.20, Fe(III) = 0.20, Ni(II) = 0.16, Pb(II) = 0.08 and Zn(II) = 0.12. The results obtained in the flow experiments, showed a recovery of ca. 100% of the metal ions adsorbed in a column packed with 2 g of SiATT, using 5 mL of 2.0 mol L-1 HCl solution as eluent. The sorption-desorption of the metal ions made possible the development of a preconcentration method and quantification by Flame AAS of metal ions at trace level in fuel ethanol.

Determination of Cu, Ni and Pb in aqueous medium by FAAS after pre-concentration on 2-aminothiazole modified silica gel

This work describes the synthesis and characterization of 2-aminothiazole modified silica gel (SiAT), and the results of a study of the adsorption and pre-concentration (in batch and using a flow-injection system coupled to an absorption atomic spectrometer) of Cu(II), Ni(II) and Pb(II) in aqueous medium. The adsorption capacities for each metal ions in mmol g-1 were: Cu(II)= 1.18, Ni(II)= 1.15 and Pb(II)= 1.10. The results obtained in the flow experiments showed a recovery of practically 100% of the metal ions adsorbed in a mini-column packed with 100 mg of SiAT, using 100 µL of 2.0 mol L-1 HCl solution as eluent. The sorption-desorption of the metal ions made possible the application of a flow-injection system for the pre-concentration and quantification by FAAS of metal ions at trace level in natural water samples digested and not digest by an oxidizing UV photolysis.

Oxigênio dissolvido (OD), demanda bioquímica de oxigênio (DBO) e demanda química de oxigênio (DQO) como parâmetros de poluição no ribeirão Lavapés/Botucatu - SP

To evaluate the depuration capacity of the Lavapes brook, which crosses Botucatu - SP, it was used dissolved oxygen (DO), biochemical oxygen demand (BOD) and chemical oxygen demand (COD) as pollution parameters. The organic pollution profile was evaluated, the depuration zone identified and hourly 24-hour collection made, the last making it possible to correlate the organic pollution with household chores. Chemical oxygen demand (COD) showed itself to be the best technique to evaluate the organic pollution profile, to identify the depuration zones and to evaluate the organic pollution punctually in this water course. Characterizing a biodegradable sewage and indicating there that is no practical addition of industrial effluents, the average relation COD/BOD was 3.4, thus making it possible to estimate the BOD by the COD. At the clean water sections, source and mouth, where de COD was below 5 mg L-1 O2 it was used the consumed oxygen values (permanganate method), which did not invalidate the depuration zones identification. However, it is necessary researches to develop the method dichromate for low levels (below 5 mg L-1 ) in order to evaluate the water stream recuperation better.

GFAAS determination of mercury in muscle samples of fish from Amazon, Brazil

In the present study, a simple, rapid and sensitive method was developed for the determination of mercury concentrations in the muscle tissue of fish from the Brazilian Amazon using graphite furnace atomic absorption spectrometry (GFAAS) following acid mineralization of the samples in an ultrasonic cold water bath. Using copper nitrate as a chemical modifier in solution and sodium tungstate as permanent modifier, we were able to attain thermal stabilization of the mercury up to the atomisation temperature of 1600 °C in the GFAAS assay. The calculated limits of detection (LOD) and quantification (LOQ) were 0.014 and 0.047 mg kg(-1), respectively.

Aplicação e modificação química da sílica gel obtida de areia

The silica gel was obtained from sand and its surface was modified with POCl3 to produce Si-Cl bonds on the silica surface. Ethylenediamine was covalently bonded onto the chlorinated silica surface. The adsorption of the chlorides of divalent cobalt, nickel and copper was qualitatively studied to show that the bonding of ethylenediamine onto the silica gel surface produces a solid base capable of chelating metal ions from solution. The experiments illustrate the extraction of silica gel, its reactivity, the development of modified surfaces and its application in removing metal ions from water and are deigned for undergraduate inorganic chemistry laboratories.

Analytical approach to the metallomic of Nile tilapia (Oreochromis niloticus) liver tissue by SRXRF and FAAS after 2D-PAGE separation: Preliminary results

An investigation was made into calcium, iron and zinc in protein spots in samples of Nile tilapia (Oreochromis niloticus) liver tissue obtained after protein separation by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and subsequent qualitative and quantitative evaluation by synchrotron radiation X-ray fluorescence (SRXRF) and Flame Atomic Absorption Spectrometry (FAAS). An analysis of the fluorescence spectra indicated the presence of calcium, iron and zinc in 12, 6 and 8 liver protein spots, respectively. The metal ions found were distributed mainly in proteins with a molar mass of less than 40.00 kDa and more than 12.00 kDa, with pI in the range of 4.70-9.40. The only exception was a spot presenting protein with a molar mass of 10.10 kDa. In addition to calcium, iron and zinc, sulfur and phosphorus - which are non-metals that may be part of the protein structure, were also detected. After microwave-assisted acid mineralization of the proteins spots, a FAAS estimation of the concentration of calcium, iron and zinc ions bound to these proteins indicated a range of 1.08-5.80 mg g(-1), 2.02-8.03 mg g(-1) and 1.60-8.55 mg g(-1), respectively.

Contribuição da cidade de Botucatu - SP com nutrientes (fósforo e nitrogênio) na eutrofização da represa de Barra Bonita

It was compared the level content of nutrients (phosphorus and nitrogen) at the Lavapes brook with level content at source an cross-tow (domestic sewage discharge) and also with the level/ content at source and mouth the Capivari river. The head-waters of the Capivari river, as well as those of the Lavapes brook, are on the highlands (at the top the sierra/ mountain-range) and its waters flow into the Barra Bonita dan on the Tiete river (Figure 1). One of its sources is near a Lavapes source and their mouths are close to each other at the Barra Bonita dam. Along the banks of both streams the use of land and the types of soil are alike, which implies in a similar rural pollution; so, what makes the difference in water quality between them is the urban pollution affecting the Lavapes brook in Botucatu. Therefore it was evaluated the contribution of nutrients (phosphorus and nitrogen) to the Barra Bonita Dam of the Capivari river and the Lavapes brook. Taking into account the domestic sewage carried into the Lavapes brrok in Botucatu, it was estimated the nutrient load of its silt (kept in its silt) and the one discharged into the Barra Bonita dam. The study- was conducted during drought, without overflows, which made it possible to measure the near-mouth-flow and to evaluate the nutrient load daily discharged into the dam. It was also evaluated the dissolved oxygen, the chemical oxygen demand and the electrical conductivity. Although the results are estimated and variabel in time we can conclude that pollution of the Lavapes brook waters with domestic sewage in Botucatu, besides making the use of its waters not viable and causing other (environmental) damage (financial losses), contributes to aggravating the eutrophication at the Barra Bonita dam.