0000000000291436
AUTHOR
A. Vértes
showing 11 related works from this author
Conversion electron Mössbauer study of low carbon steel polarized in aqueous sulfate and sulfite containing sulfate solutions
1993
Abstract The passivation of low carbon steel was studied in aqueous solutions of 0.5 M Na 2 SO 4 (pH = 3.5 and 6.5) and of 0.5 M Na 2 SO 4 + 0.001 M NaHSO 3 (pH 3.5 and 6.5). The used conversion electron Mossbauer spectroscopy (CEMS) with the complementary electrochemical, microscopic and spectrophotometric investigations proved that the presence of sulfite ion induces pitting corrosion. The compositions and thichnesses of the passive films formed during the electrochemical treatments are determined from the conversion electron Mossbauer spectra. γ-FeOOH was found in each case as a major component. At pH = 3.5, the sextet belonging to Fe 3 C appears in the spectra in most cases, and also Fe…
Icems and dcems study of Fe layers evaporated onto Al and Si
1990
Thin layers of57Fe (2.5 nm, 10 nm and 70 nm thickness), vacuum evaporated onto Al and Si plates, have been investigated by conversion electron Mossbauer spectroscopy (CEMS). The measurements were performed employing both a proportional counter and a channeltron for conventional and ultrahigh-vacuum integral CEMS (UHV-ICEMS) studies, respectively, and a channeltron for depth-selective CEMS (DCEMS). The phase analysis of the layers on base of experimental results has indicated the presence of metallic iron and one or two iron compounds, ascribed to iron reaction products formed with the residual gas during evaporation. These products are most likely rather stable iron nitrides, are more or le…
A study of thin surface layers by multilayer Mössbauer spectroscopy /MMS/
1990
A stacking Mossbauer technique, MMS has been applied for studying thin surface layers. The surface layers formed on the57Fe film in aqueous solutions of corrosion inhibitors, such as zinc phosphate and barium metaborate, and in distilled water was studied by this method. It has been found that the corrosion is much slower in the presence of zinc phosphate and barium metaborate. XPS analysis suggests the formation of a mixed iron zinc phosphate on the surface of the57Fe film after corrosion in a zinc phosphate solution.
A Mössbauer study of the crystalline structure of the passive film formed on iron in aqueous sulfate solution containing sulfite in low concentration
1993
Electrochemically induced passivation of evaporated, enriched 57Fe in 0.5 mol dm−3 Na2SO4 + 0.001 mol dm−3 NaHSO3 aqueous solution (pH 6.5) was followed by conversion electron Mossbauer spectroscopy. The transformation of amorphous iron oxide or hydroxide into crystalline γ-FeOOH could be observed with the increase of the polarization time. The comparison of the original quantity of evaporated, enriched 57Fe layer on the surface of the samples with the dissolved iron, measured in the solutions after the polarization, proved the existence of pitting corrosion at this pH.
In-situ radiotracer studies of sorption processes in solutions containing (bi)sulfite ions—II. Low carbon steel
1997
Abstract In this paper, time, potential and pH dependence of SO42− and HSO3− accumulations measured by an in-situ radiotracer method on surface oxide layers of low carbon steel are presented and discussed. This work is a continuation of a research program[1–5] and deals with the characterization of the sorption behaviour of low carbon steel in solutions containing sulfate and bisulfite ions (as a possible model of acid rain). From the experimental results it can be stated that 1. (i) the presence of bisulfite ions in the solution phase accelerates the corrosion of low carbon steel; 2. (ii) at E > 0.40 V the electrooxidation of HSO3− ions presumably proceeds to yield a steel surface covered …
Influence of sulphite on the passivation of iron
1991
Abstract Mossbauer spectroscopy and electrochemical measurements were used to study the passivation of iron and steels in a sulphite containing solution. The potentiodynamic curves show that passivation occurs at −140 mV potential vs saturated calomel electrode ( sce ). The main phase of the passive layer was found to be γ-FeOOH, while FeSO 4 ·H 2 O on the surface and FeSO 3 ·3H 2 O inside the layer were identified as minor phases in the case of polarization in a solution of pH 3.37. Only γ-FeOOH was observed on the surface of samples polarized at pH 6.6.
Short range ordering and phase separation in rapidly quenched Ni80 57Fe1P19 amorphous alloys solution treated at different temperatures
1990
Abstract Electrochemical measurements and Mossbauer spectroscopy were used to study a rapidly quenched Ni80 57Fe1P19 amorphous alloy solution treated between 920 and 1500 °C. Different short range orderings were shown in amorphous alloys solution treated at different temperatures. This finding can be associated with phase separation occurring in the liquid state. This phase separation can be inherited in slightly relaxed amorphous state.
Electrochemical and conversion electron mössbauer study of corrosion induced by acid rain
1993
Abstract The passivation of low carbon steel was studied in aqueous solution of 0.5M Na2SO4 +0.001M NaHSO3 (pH 3.5, 6.5 and 8.5) which can be considered as a model of acid rain. The used conversion electron Mossbauer spectroscopy (CEMS) with the complementary electrochemical investigations proved that the sulfite ions induce pitting corrosion at pH 3.5 and 6 5 while the measurements showed much weaker pitting at pH 8.5. The compositions and thicknesses of the passive films formed during the electrochemical treatments are determined from the CEM spectra. Only γ-FeOOH was found on the surface of the samples at pH 6.5 and 8.5. Nevertheless, at pH 3.5 the sextet belonging to Fe3C appears in the…
conversion electron Mössbauer study of low carbon steel polarized in aqueous sulfate solution containing sulfite in low concentration
1992
The passivation of low carbon steel was studied in aqueous solution of 0.5 M Na2SO4+0.001 M NaHSO3 at pH=3.5 and 6.5. The found major components at pH-3.5 were: γ-FeOOH and Fe3C, and also FeSO4.H2O could be identified on the surface of the low carbon steel as a minor component. At pH-6.5, the passive film contained only amorphous iron(III)-oxide or oxyhydroxide.
A study of electrochemically-induced corrosion of low carbon steel in a medium modelling acid rain
1994
Complementary electrochemical, spectrophotometric and electron microsopic investigations were made in addition to the conversion electron Mossbauer spectroscopic (CEMS) measurements to learn more about the mechanism of corrosion of low carbon steel samples in aqueous sulfate and sulfite containing sulfate solutions (pH 3.5, 6.5 and 8.5). Passivation of iron in pure sulfate solution was studied in detail in earlier papers. In the present work, we used a solution containing both sulfate and sulfite anions to obtain more information about the effect of acid rain on low carbon steel samples. The compositions and thicknesses of the passive films formed due to the electrochemical treatments were …
Dynamics of BF 4 - anion reorientation in the spin-crossover compound [Fe(1-n-propyl-1H-tetrazole) 6 ](BF 4 ) 2 and in its Zn II analogue
1999
19 F and 11 B spin-lattice relaxation times were measured in [ Zn ( ptz ) 6 ] ( BF 4 ) 2 and in the spin-crossover compound [ Fe ( ptz ) 6 ] ( BF 4 ) 2 . For both compounds BF 4 - anion reorientation is active above 50 K. For [ Zn ( ptz ) 6 ] ( BF 4 ) 2 , the anion-reorientation dynamics is different in the temperature regions of 50-90 K, 90-120 K, and above 150 K; between 120 and 150 K it changes rapidly reflecting a structural change. In [ Fe ( ptz ) 6 ] ( BF 4 ) 2 the mechanism for the paramagnetic relaxation involving the 19 F nuclei is found to be of the diffusion-limited type according to the theory of Lowe and Tse. The present results prove that the spin-crossover takes place in a dy…