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Determination of hydrogen peroxide based on a metal dispersed sol-gel derived ceramic-graphite composite electrode.

A new copper dispersed ceramic-graphite composite electrode was fabricated by the initial mixing of copper nitrate and (3-mercaptopropyl)trimethoxy silane (MPS) followed by stirring with graphite powder. The combination of the metal catalysis and the advantages of the ceramic composite favored the electrocatalytic reduction of hydrogen peroxide (H2O2) at a reduced overpotential of -0.2 V with good sensitivity, stability and reproducibility. The sensor showed a good linear response to H2O2 in the range from 8.3 x 10(-6) M to 2.0 x 10(-3) M with a correlation coefficient of 0.9989 and the detection limit was 6.2 x 10(-6) M (S/N =3).

Journal Article↗

Freon (CHF3)-assisted atomization for the determination of titanium using ultrasonic slurry sampling-graphite furnace atomic absorption spectrometry (USS-GFAAS): a simple and advantageous method for solid samples.

A simple and advantageous method for the determination of titanium using graphite furnace atomic absorption spectrometry with slurry sampling has been developed. Titanium is one of the refractory elements that form thermally stable carbides in the graphite tube, which leads to severe memory effects. Trifluoromethane (Freon-23) was applied in the purge gas during the atomization step or alternatively just prior to the atomization to successfully eliminate the problems of carbide formation and increase the lifetime of the furnace tube which could be used for more than 600 heating cycles. A flow rate of 40 mL min(-1) (5% of Freon in argon) was used to obtain symmetrical peaks with no tailing. However, when the gas flow rate was too high (250 mL min(-1)) the peak-tailing and memory effects reappeared. Ti was determined in various materials covering a wide range of concentrations, from 2.8 microg g(-1) to 12% (m/m) Ti. The accuracy of the method was confirmed by analyzing certified reference materials (CRMs) or by comparing the results with those obtained using inductively coupled plasma-atomic emission spectrometry (ICP-AES) after decomposition of the samples. The materials analyzed were soil, plant, human hair, coal, urban particulate matters, toothpaste, and powdered paint.

Journal Article↗

Analytical application of 2f-wavelength modulation for isotope selective diode laser graphite furnace atomic absorption spectroscopy.

Experiences in the analytical application of the 2f-wavelength modulation technique for isotope selective atomic absorption spectroscopy in a graphite furnace are reported. Experimental as well as calculated results are presented, mainly for the natural lithium isotopes. Sensitivity, linearity, and (isotope) selectivity are studied by intensity modulation and wavelength modulation. High selectivities can be attained, however, on the cost of detection power. It is shown that the method enables the measurement of lithium isotope ratios larger than 2000 by absorption in a low-pressure graphite tube atomizer.

Journal Article↗

Determination of Al, Cu, Li and Mn in spruce seeds and plant reference materials by slurry sampling graphite furnace atomic absorption spectrometry.

An ultrasonic slurry sampling graphite furnace AAS method was developed for the determination of Al, Cu, Li and Mn in spruce seeds, NBS SRM 1575 pine needles and GBW CRM 07602 bush branches and leaves. The only sample preparation was grinding in a Mixer Mill before preparing a slurry by adding 0.14 mol/L nitric acid to a small sample aliquot. Cryogenic grinding was used for the spruce seeds to solve the problem of agglomerating during grinding at room temperature. A modified sample tray was applied allowing the use of both the commercial 1.5 mL vials and home-made 15 mL vials. With optimal conditions for ultrasonic agitation the homogeneity and particle size distributions in the slurries prepared in the two different vials were similar. Several aspects of the slurry sampling approach are discussed and data of important parameters are given, including the total number of particles injected into the graphite furnace, densities of the materials and percentage of analyte extracted into the liquid phase of the slurry. The density of the materials was determined by two methods; by using a Coulter particle analyser and by using a gravimetric method. The two methods gave similar accuracy and precision. The concentration ranges of the elements (in microg g(-1)) were: 80-2100 for Al, 3-15 for Cu, 0.06-2.5 for Li and 50-700 for Mn. External calibration with aqueous standards was employed. Chemical modifiers were not found to be necessary. The relative standard deviations were in the range 1.7-7%. Analyses of the two certified plant reference materials confirmed the accuracy of the method. In addition no significant difference was found for analyses of digested and slurried spruce seeds. The detection limit was 10 ng g(-1) for Li and 170 ng g(-1) for Cu. The characteristic mass (area measurements) was 4.4 pg for Li and 11 pg for Cu. For Al and Mn less sensitive wavelengths were used.

Metals↗

PbO2-based graphite-epoxy electrode for potentiometric determination of acids and bases in aqueous and aqueous-ethanolic media.

The construction and analytical evaluation of a PbO2-based graphite-epoxy electrode sensitive to H3O+, based on incorporation of lead(IV) oxide in a graphite-epoxy matrix, are described. The data obtained from a variety of acid-base titrations in aqueous and aqueous-ethanolic media were compared with those obtained by use of a glass electrode under the same conditions. The proposed electrode provides a linear response in the pH range from 1 to 11 with a slope of -58.7+/-0.3 mV pH(-1) and -60.8+/-0.2 mV pH(-1) in aqueous and ethanolic media, respectively. The response time was less than 15 s and the lifetime of the electrode was at least eight months (ca. 5000 determinations) and its performance is good in pH determination and end-point detection in potentiometric acid-base titrations in both aqueous and aqueous-ethanolic media.

Journal Article↗

Direct determination of silicon in powdered aluminium oxide by use of slurry sampling with in situ fusion graphite-furnace atomic-absorption spectrometry.

A direct method for determination of silicon in powdered high-purity aluminium oxide samples, by slurry sampling with in situ fusion graphite-furnace atomic-absorption spectrometry (GF-AAS), has been established. A slurry sample was prepared by 10-min ultrasonication of a powdered sample in an aqueous solution containing both sodium carbonate and boric acid as a mixed flux. An appropriate portion of the slurry was introduced into a pyrolytic graphite furnace equipped with a platform. Silicon compounds to be determined and aluminium oxide were fused by the in situ fusion process with the flux in the furnace under optimized heating conditions, and the silicon absorbance was then measured directly. The calibration curve was prepared by use of a silicon standard solution containing the same concentration of the flux as the slurry sample. The accuracy of the proposed method was confirmed by analysis of certified reference materials. The proposed method gave statistically accurate values at the 95% confidence level. The detection limit was 3.3 microg g(-1) in solid samples, when 300 mg/20 mL slurry was prepared and a 10 microL portion of the slurry was measured. The precision of the determination (RSD for more than four separate determinations) was 14% and 2%, respectively, for levels of 10 and 100 microg g(-1) silicon in aluminium oxide.

Aluminum Oxide↗

Emission of M2X+ cluster ions in thermal ionization mass spectrometry in the presence of graphite.

The emission of M2X+ cluster ions in thermal ionization mass spectrometry when graphite is loaded on the heating filaments was studied. The emission model of non-reductive thermal ionization of graphite was preliminarily discussed and factors influencing the thermal emission of M2X+ ions were investigated. The results show that the intensities of M2X+ cluster ions are related to ionic radius and crystal lattice energy, and possibly also to the solvation energies of ions. The intensities of M2Cl+ (M stands for K, Rb, and Cs) cluster ions, the M2Cl+/M+ ratios, and the 37Cl/35Cl ratios determined from M2Cl+ ion measurement usually increase with measurement time. The variation of the 37Cl/35Cl ratios determined from Cs2Cl+ ion measurement is lower than those based on K2Cl+ and Rb2Cl+ ion measurement, indicating the lowest isotopic fractionation.

Journal Article↗

Determination of cadmium and copper with ET-AAS after electrochemical deposition on a graphite electrode.

The electrodeposition of cadmium and copper on a special graphite disk electrode has been performed at controlled potential. The electrode with the deposit has been inserted into the graphite atomizer HGA-400 by an adapted automatic sampler for the final determination by ET-ASS. The sensitivity of determination has been 0.371 (microg l(-1))(-1) for cadmium and 0.025 (microg l(-1))(-1) for copper for 2 min electrodeposition and increased linearly with the time of deposition. The limit of detection (3s(bl)) has been 7.9 ng l(-1) Cd(2+) and 0.11 microg l(-1) Cu(2+) for 2 min deposition and it has been improved with increased time of electrodeposition. The technique has been applied to the determination of both metals in seawater and to speciation in the presence of EDTA complexing agent.

Journal Article↗

Atomic-focuser Imaging by Graphite Crystals in Carbon Nanoshells.

One of the atomic-focuser modes for ultra-high resolution electron microscopy is described theoretically and illustrated by the observation of images formed within the diffraction spots of nanodiffraction patterns of carbon nanoshells. In this mode, the specimen is illuminated by the focused probe of a scanning transmission electron microscope and is followed by a thin crystal at a Fourier-image distance. The theory shows that each diffraction spot of the crystal contains a magnified image of the illuminated area of the specimen, having a resolution depending on the width of the intensity peak of electrons channeled along atomic rows in the crystal. A thin graphite crystal, contained within one wall of a carbon nanoshell, can act as an atomic focuser to image part of the other wall of the nanoshell, or tungsten atoms deposited on this wall. Simulations of the transmission of electrons through graphite crystals show that the images formed should have a resolution of about 0.06 nm. Experimental images suggest that this resolution has been attained in the imaging of tungsten atoms or clusters of tungsten atoms.

Journal Article↗

Solid-phase extraction of polar pesticides from environmental water samples on graphitized carbon and Empore-activated carbon disks and on-line coupling to octadecyl-bonded silica analytical columns.

The suitability of Empore-activated carbon disks (EACD), Envi-Carb graphitized carbon black (GCB) and CPP-50 graphitized carbon for the trace enrichment of polar pesticides from water samples was studied by means of off-line and on-line solid-phase extraction (SPE). In the off-line procedure, 0.5-2 l samples spiked with a test mixture of oxamyl, methomyl and aldicarb sulfoxide were enriched on EnviCarb SPE cartridges or 47 mm diameter EACD and eluted with dichloromethane-methanol. After evaporation, a sample was injected onto a C18-bonded silica column and analysed by liquid chromatography with ultraviolet (LC-UV) detection. EACD performed better than EnviCarb cartridges in terms of breakthrough volumes (> 2 l for all test analytes), reproducibility (R.S.D. of recoveries, 4-8%, n = 3) and sampling speed (100 ml/min); detection limits in drinking water were 0.05-0.16 microgram/l. In the on-line experiments, 4.6 mm diameter pieces cut from original EACD and stacked onto each other in a 9 mm long precolumn, and EnviCarb and CPP-50 packed in 10 x 2.0 mm I.D. precolumn, were tested, and 50-200 ml spiked water samples were preconcentrated. Because of the peak broadening caused by the strong sorption of the analytes on carbon, the carbon-packed precolumns were eluted by a separate stream of 0.1 ml/min acetonitrile which was mixed with the gradient LC eluent in front of the C18 analytical column. The final on-line procedure was also applied for the less polar propoxur, carbaryl and methiocarb. EnviCarb could not be used due to its poor pressure resistance. CPP-50 provided less peak broadening than EACD: peak widths were 0.1-0.3 min and R.S.D. of peak heights 4-14% (n = 3). In terms of analyte trapping efficiency on-line SPE-LC-UV with a CPP-50 precolumn also showed better performance than when Bondesil C18/OH or polymeric PLRP-S was used, but chromatographic resolution was similar. With the CPP-50-based system, detection limits of the test compounds were 0.05-1 microgram/l in surface water.

Adsorption↗

Electrochemical behaviour of proteins at graphite electrodes. II. Electrooxidation of amino acids.

Electrochemical oxidation of L,alpha-amino acids at a paraffin-wax impregnated spectroscopic graphite electrode (WISGE) was studied by means of linear sweep, cyclic, phase-sensitive alternating current and differential pulse voltammetric techniques. It was found that out of the amino acids usually occurring in proteins only tyrosine, tryptophan, histidine, cystine, cysteine and methionine were oxidized at the WISGE. At relatively low concentrations of amino acids (up to ca. 2 x 10(-4) M) the electrode process in which the amino acids are oxidized at the WISGE has the characteristics of an irreversible reaction controlled by diffusion. Coulometric measurements showed that oxidation of tyrosine and tryptophan at the WISGE, i.e. of amino acids which are responsible for the oxidizability of proteins at graphite electrodes, is a two-electron process. At higher concentrations of tyrosine-and tryptophan (above ca. 2 x 10(-4) M) adsorption of the oxidation product of these amino adds was demonstrated.

Journal Article↗

Determination of organosilicon oxide polymers in tissue by atomic absorption spectroscopy using HGA graphite furnace.

A simple method of extraction and determination of organosilicon oxide polymers (silicones) in 0.1-0.5 g of formalin fixed tissue by atomic absorption spectroscopy is described. Before the tissue is extracted with n-heptane, it is dried in a desiccator containing concentrated sulphuric acid. The graphite tubes in the HGA graphite furnace are tubes with L'vov platform. The evaporation of n-heptane and a part of the charing of the tissue extract in the tube are done in the presence of oxygen (air). The significance of the employment of L'vov platform and the presence of oxygen are discussed. The methods detection limit (2 X S.D.) is about 0.009 microgram silicon/ml tissue extract which corresponds to about 0.5 microgram polydimethylsiloxane/g tissue.

Dimethylpolysiloxanes↗

Preparation and physicochemical and electrochemical characterization of exfoliated graphite oxide.

Exfoliated graphite oxide (EGO) is prepared by oxidizing exfoliated graphite (EG) using a mixture of KMnO(4)/H(2)SO(4). The physicochemical characterization of the EGO has been carried out using FT-Raman, FT-IR, XPS, NMR, and diffraction techniques. Colloidal form of EGO is subsequently prepared by ultrasonicating EGO in water. Thin films of EGO on a glassy carbon/gold surface are formed and the electrochemical and ion exchange properties have been studied using various redox systems such as K(4)[Fe(CN)(6)], ascorbic acid, and dopamine. The charge-based adsorption properties can be made use of, to either suppress or catalyze ascorbic acid oxidation. Adsorption and preconcentration of dopamine on the EGO film has been shown to electrocatalyze the oxidation of NADH.

Journal Article↗

Determination of silver in biological samples using graphite furnace atomic absorption spectrometry based on Zeeman effect background correction and matrix modification.

A method for the determination of silver in human body fluids and biological material is described. The silver in an acid digest of biological samples and diluted body fluids is quantified using Zeeman graphite furnace atomic absorption spectrometry (ZGFAAS). The effects of NH4H2PO4 as matrix modifier and standard addition are discussed. Atomization from the graphite tube wall and from the pyrolytical tube with platform is also discussed and the peak height and the peak area are compared. The best results were achieved by using matrix modification, stabilized temperature platform furnace, integrated absorbance and standard addition technique. The calibration was linear up to 15 micrograms X L-1; the between-run precision was 5.9% at 40 micrograms X kg-1 of silver.

Animals↗

Determination of surface heterogeneity profiles on graphite by finite concentration inverse gas chromatography.

Inverse gas chromatography (IGC) is an established tool in the determination of the adsorption potential distribution function. This function reflects the energetic heterogeneity profile of a surface and therefore provides interesting information on the nature and population of different surface sites. IGC is shown to be a fast and accurate technique for the determination of the adsorption potential distribution function of two different graphite samples. In this paper the adsorption of acidic and basic organic vapours is studied. Unlike heterogeneity profiles determined by nitrogen measurements, experiments with polar vapours can provide additional information on the adsorption mechanism and polar sorption sites. The heterogeneity profiles of all probes used are significantly different from one another and allow discreet energy levels to be distinguished. Chemically different probes reveal different adsorption mechanisms for the graphite surface.

Adsorption↗

Liquid chromatography analysis of phosphonic acids on porous graphitic carbon stationary phase with evaporative light-scattering and mass spectrometry detection.

The analysis of several phosphonic acids has been investigated by liquid chromatography (LC), using porous graphitic carbon as stationary phase with mass spectrometry (MS) or evaporative light-scattering detection (ELSD). In both detection modes (MS and ELSD), the mobile phase must be volatile and, due to the porous graphitic carbon (PGC) properties, should promote electronic interactions. Among the various hydrogeno- and perfluorocarboxylic acids tested, trifluoroacetic acid (0.1%, v/v) was selected as electronic competitor for solute retention. The baseline resolution of a phosphonic acids mixture required a trifluoroacetic-acetonitrile gradient elution. This methodology was then applied to the identification of phosphonic acids in a spiked tap water sample. Quantitative analyses are successfully achieved with a good correlation coefficient.

Carbon↗

Determination of trace lithium in biological fluids using graphite furnace atomic absorption spectrophotometry: variability of urine matrices circumvented by cation exchange solid phase extraction.

A graphite furnace atomic absorption spectrometry method has been developed for the quantitative determination of submicromolar endogenous concentration of lithium in human plasma and urine using pyrolitically-coated graphite tubes in combination with ammonium nitrate matrix modification. This latter treatment could not completely abolish the interferences caused by the matrix, notably in urine samples. The variability of the urinary matrices required an additional standardization procedure by solid-phase extraction on strongly acidic cation exchange cartridges. Matrix-matched samples were used for the establishment of calibration curves with the addition-calibration method. Calibration curves were linear up to 0.72 mumol/l (1.0 > r2 > 0.99). The described method enables accurate measurements of trace-lithium in biological samples at concentrations down to 0.03 mumol/l with intra- and inter-day variabilities < 10%. The method was applied to the determination of trace-lithium levels in urine and plasma samples from healthy individuals enabling the calculation of its fractional excretion (FeLi) (median range 17.3%), a value which reflects the functional capacity of the kidney to reabsorb sodium and water at the proximal tubular portion of the nephron. This sensitive method can thus be used as an investigative and diagnostic tool in various renal pathophysiological conditions, in clinical research, and may also be applied to studies on the trace-lithium status of population in connection with psycho-affective disorders.

Cations↗

Microwave excitation of ultrasound in graphite-fiber reinforced composite plates.

In this paper is demonstrated the effect of microwave beam polarization on the thermal generation of acoustic waves in continuous fiber-reinforced composite laminates. It is found that beam polarization strongly influences the dielectric interaction that leads to thermal losses, bulk expansion, and acoustic wave generation. The oriented graphite fibers in the composite laminate effectively short the microwave fields and reduce the generation efficiency nearly to zero. Ultrasonic waves at several hundred kHz generated in the composite are detected by air-coupled acoustic transducers located on the opposite side of the plate specimen from the 9.41 GHz incident microwave beam. With some averaging signal-to-noise ratios of better than 26 dB are obtained. Applying a conventional model of electromagnetic wave scattering in anisotropic media to this experiment yields good agreement between calculations and measured data. Implications for microwave-acoustic testing of graphite-reinforced composites are also discussed.

Journal Article↗