Search results for "nitric acid"
showing 10 items of 49 documents
Atomic Absorption Spectrophotometric Determination of Cobalt in Foods
1985
A method is reported for determination of chromium in foodstuffs. Organic matter is digested with nitric acid, followed by oxidation to Cr(VI) and extraction with methyl isobutyl ketone (MIBK) after HCl addition. Chromium determinations are performed by flame absorption spectroscopy. Absence of interferences is verified and recovery tests are performed on food samples. Quantitation limit (3.8 ng/mL), accuracy (NBS Standard Reference Material 1,573 Tomato Leaves, 4,500 +/- 500 ng/g, found 3,860 +/- 409 ng/g), and precision (CV for vegetable matrix = 9.05%, CV for animal matrix = 14.95%) of the procedure are evaluated.
Removal of trivalent chromium from tannery waste waters using bone charcoal
2002
International audience; The ability of bone charcoal to remove Cr(III) from aqueous solutions by adsorption has been investigated. The adsorbent used was first characterised and then the adsorption was studied as a function of time and amount of charcoal. Tests were carried out with synthetic solutions whose Cr concentrations (500 mg L-1) were similar to those found in some effluents of Moroccan tannery industries. Cr removal efficiencies higher than 90% were obtained at pH 3.5 using 3 g of bone charcoal and a stirring time of about 30 min. Results of Cr removal by all sieved fractions of bone charcoal had shown the same interesting capabilities for Cr(III) retention. The cross interference…
Raman investigation of single oxidized carbon nanotubes
2001
The oxidation process of single-walled carbon nanotubes via nitric acid treatment was followed by IR-, UV-Vis-NIR, and single bundle Raman spectroscopy. The introduction of functional, oxygen-containing groups is revealed by an additional absorption band at 1725 cm−1, characteristic of carbonyl stretch vibrations. No significant shift of the optical absorption bands could be detected after oxidation. The combination of atomic force microscopy and confocal scanning resonance-enhanced Raman microscopy was used to investigate thin bundles and, eventually, individual nanotubes in detail. These experiments enabled determination of the dependence of the Raman intensity of the G-line (around 1590 …
Detection of reactive nitrogen containing particles in the tropopause region? Evidence for a tropical nitric acid trihydrage (NAT) belt
2008
The detection of nitric acid trihydrate (NAT, HNO<sub>3</sub>&times;3H<sub>2</sub>O) particles in the tropical transition layer (TTL) harmonizes our understanding of polar stratospheric cloud formation. Large reactive nitrogen (NO<sub>y</sub>) containing particles were observed on 8 August 2006 by instruments onboard the high altitude research aircraft M55-Geophysica near and below the tropical tropopause. The particles, most likely NAT, have diameters less than 6 &mu;m and concentrations below 10<sup>-4</sup> cm<sup>&minus;3</sup>. The NAT particle layer was repeatedly detected at altitudes between 15.1 and 17.5 km ove…
Nanostructure Formation on ZnSe Crystal Surface by Electrochemical Etching
2021
The article describes a simple method for nanostructuring the surface of monocrystalline zinc selenide. It is shown that the traditional electrochemical etching of n-ZnSe (111) samples in a concentrated solution of nitric acid leads to the appearance of massive etching pits and small pores on the surface. The dynamics of the process and stages of crystal dissolution has been studied. It is assumed that the porous zinc selenide obtained in this way can be used in optoelectronic structures, as well as as buffer layers for growing zinc oxide.
Determination of carbonates in waters by on-line vapor generation FTIR
1998
Abstract An electrically heated gas-permeation unit (GPU) has been employed for the vapor-generation Fourier transform infrared (FTIR) determination of total carbonate in waters. The developed method is based on the simultaneous injection of 100 μ l sample and 100 μ l nitric acid in a two-channel manifold with a merging zone, which provides the generation of CO 2 through the GPU, heated at 90°C, from which CO 2 is swept by a stream of N 2 to a long-path infrared gas cell. Absorbance measurements were made in the range from 2500 to 2150 cm −1 and the corresponding flow injection recordings were obtained as a function of time. The areas of these peaks are interpolated in a calibration equatio…
Atomic absorption spectrometric determination of molybdenum in lubricating oils with use of emulsions
1985
Abstract Samples (0.1 g) containing molybdenum disulphide are digested with aqua regia or with a (1 + 1) hydrofluoric/nitric acid mixture, without complete destruction of the matrix, and the molybdenum is determined in an air/acetylene flame, after emulsification with a non-ionic surfactant (Nemol K-39). The detection limit is ca. 30 μg Mo g−1, and the r.s.d. is 2.9% for 6 analyses of a sample containing 6.5 mg Mo g−1.
Direct determination of lead in human milk by electrothermal atomic absorption spectrometry
1999
Abstract Infants are particularly sensitive to the toxic effects of lead. Since milk is their only or main food it is important to know the contribution of milk to lead intake. The purpose of this study was to develop a direct method for determining the lead content of human milk by electrothermal atomic absorption spectrometry when a deuterium lamp is the only background correction available. The optimum conditions for lead determination in breast milk: sample dilution in Triton ×-100, modifier (75 μg of palladium) and nitric acid contents (2%) and the graphite furnace program (mineralization: 1100°C; atomization: 2300°C) were selected. The analytical parameters are: linearity (20–300 ng m…
Chemiluminometric photo-induced determination of Strychnine in a Multicommutation flow assembly
2007
This paper deals on the determination of Strychnine, a potent and dangerous pesticide and the analytical procedure is based on the photo-induced chemiluminescence of the pesticide by means of the Multicommutation continuous-flow methodology. Small segments of the pesticide solution were sequentially alternated with segments of the solution for adjusting the suitable medium for the photodegradation. The required time of UV irradiation was obtained by stopped-flow during 150 s; then, the resulting solution formed alternated segments with the oxidizing solution containing 5 × 10−3 mol l−1 Ce(IV) in 0.6 mol l−1 nitric acid. The calibration range, from 2 μg l−1 to 50 mg l−1, resulted in a linear…
Chemiluminometric determination of the pesticide 3-indolyl acetic acid by a flow injection analysis assembly
2005
Abstract A new method is proposed for the chemiluminescent determination of the pesticide 3-indolyl acetic acid by means of an flow injection analysis system. The chemiluminescence emission is obtained by oxidation of the analyte with Ce (IV) in nitric acid and presence of β-cyclodextrine. The continuous-flow method allows the determination of 159 samples h−1 of 3-indolyl acetic acid in an interval of concentrations over the range 0.5–15.0 mg l−1. The limit of detection was 0.1 μg l−1 and the R.S.D. (n, 17) at 2.0 mg l−1 of the pesticide level was 2.7%. The method was applied to water samples.