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Organisationseinheit der BAM
Eingeladener Vortrag
- nein (10)
Radical species like CO-2,CO-3, SO-2, and SO-3 can be created by exposing natural and synthetic calcium carbonates to sunlight or to the light of a Hg(Xe) lamp. This poses as a risk for ESR dating of these materials, because the radicals formed by light exposure cannot be distinguished from those generated by radioactivity. Furthermore, paramagnetic centers like SO-2, electrons trapped near Zn2+ or Cd2+ ions, surface defects, and radicals with g?=2.0040, can be bleached in ?-irradiated samples by light and show conversion effects.
Radiation defects in alkaline earth silicate glasses are studied by means of ESR and optical spectroscopies. Previously undiscovered relations between findings of both methods are deduced using four different experimental tools: (i) variation of chemical glass composition; (ii) isochronal annealing of ggr-irradiated samples; (iii) optical bleaching of ggr-irradiated samples; (iv) variation of the ggr-dose. Oxygen hole centres are mainly responsible for the radiation induced absorption in the visible part of the optical spectrum. Previously undescribed electron centres with broad and asymmetric ESR resonances (gprime=1·955) contribute to the optical spectra (2002000 nm) in a small way. It is suggested they are electrons trapped on small aggregates of alkaline earth ions. The radiation induced recharging of incorporated Fe3+ ions is also evidenced by optical and ESR spectroscopies. Fe3+ ions react as electron traps forming not only Fe2+ but also {Fe3+}- species which might be responsible for an absorption band at 300 nm. A correlation was found between the changes of intensity with those of the ESR spectroscopically detected Fe3+ content of the samples.
Direct coupling of an excimer laser to the cavity of an X-band ESR spectrometer enabled in situ observation of ultraviolet irradiation (248 nm) induced effects in aluminosilicate glasses. Under these conditions the radiation was absorbed by iron traces present in the glasses and finally electron/hole pairs were formed. The trapping and detrapping of electrons and holes, e.g. generation and decay of paramagnetic defects, could be followed in dependence on repetition rate of the laser (120 Hz), temperature during irradiations (4·2300 K) and composition of the glasses. The holes were trapped at SiO and AlOSi sites. Zn2+ and Cd2+ ions (likely as parts of ZnO or CdO aggregates) as well as Fe3+ ions served as effective electron traps. Additionally, changes of the dielectric properties of the samples during and after ultraviolet irradiations could be monitored directly. These are large if relatively mobile ions (e.g. Na+) are present in the sample. Comparison of ultraviolet to -irradiated samples shows that the type of traps present in the samples mainly depends on the glass composition. However, the relative amounts of stabilised holes and electrons essentially depend on the conditions and parameters of irradiation.
Glasses in the systems Li2OB2O3V2O5 and ZnOB2O3V2O5 as well as crystalline reference substances were investigated by V-K-EXAFS. The glasses have a high modifier content ([Li2O, ZnO]/[B2O3] ratio>1) and contain 1050 mol% V2O5. The VO interatomic distance, coordination number and DebyeWaller factor were determined from the analysis of the measured absorption spectra. In the glasses investigated (and in binary lithium or zinc vanadate glasses too) VO4 tetrahedra are the predominant coordination polyhedra for the vanadium ions. The symmetry of the tetrahedra is more or less distorted in comparison to crystalline substances. The VO4 tetrahedra can be either directly connected to each other or incorporated into borate BO3/BO4 groupings. Structural elements which are comparable to those in crystalline substances can be discussed. In glasses of the metaborate composition, vanadium can be incorporated in chain or ring [BØ2O-]n metaborate groupings. With increasing V2O5 content the vanadium ions can extensively replace boron ions and form distorted tetrahedra in VØ2O2- metavanadate groups. In glasses of high modifier content and low vanadium amount the vanadium ions create nearly regular tetrahedra of isolated VO43- ortho- or V2ØO64- pyrovanadate groups in the presence of B2ØO44- pyroborate, BO33- orthoborate and BØ4- groups.
Electron paramagnetic resonance (EPR) of Fe3+ ions in Al2O3 is studied in powder samples prepared by different routes and/or modified by thermal or mechanical treatments, with different doping levels and grain sizes. The measurements are performed in various frequency bands (S, X, K, Q and W) and with bimodal detection in X-band. Simulations of the spectra are achieved with a code designed for computing EPR powder spectra described by any spin Hamiltonian including second-, fourth-and sixth-order ZFS terms (S ? 7/2). The linewidths, intensities and lineshapes are accounted for. The lineshape is Gaussian at low Fe3+ concentration whereas it is Lorentzian for higher concentration. The linewidths are interpreted as the superimposition of three main contributions: intrinsic linewidth, dipolar broadening and broadening due to lattice imperfections. The latter is tentatively interpreted in terms of quadrupolar spin Hamiltonian parameter distributions treated using first-order perturbation theory. Whatever the sample, only the b22 spin Hamiltonian parameter is found to be distributed around a mean zero value which corresponds to rhombic distortions. Angle and bond length distributions are tentatively extracted from the b22 distributions which gives some insight into the local order around the spin probe in relation to the preparation and treatment of the samples.
We have carried out some laboratory experiments to establish possibilities to melt 16Na2O*10CaO*74SiO2 glasses from consisting of mainly quarz sands of Buir nuur lake. When the sands used directly, the formed glasses had slight blue colour, the origin of which may be connected with aluminium and iron impurities in the sands. Presence of these impurities is confirmed by chemical analyse and ESR study data. Allso have been studied liquid gas extraction phenomena in the sands and melted glass samples and determined some physical properties of them.
The transformation of doped or seeded pseudoboehmite to corundum was studied by combining thermal analysis, X-ray diffraction, transmission electron microscopy, and electron paramagnetic resonance spectroscopy. The temperature of phase transformation to corundum was lowered by about 130 °C when Fe3+ or corundum seeds were added to the sols. Action of Fe3+ ions depends on the actual degree of thermally induced transformation of pseudoboehmite via transition aluminas to corundum and the ability of these alumina phases to incorporate Fe3+ ions. These ions tend to aggregate with increasing iron concentration of the alumina phases and can work as nucleation centers. Small (not, vert, similar20 nm) corundum particles act as active nucleation sites whereas larger grains (200400 nm) also present in the samples are less effective. For the first time trapping and stabilization of NO2 molecules in transition aluminas formed by a solgel route was shown.
The role of Fe3+ ions in the transformations from boehmites and pseudoboehmite xerogels via transition aluminas to corundum was studied here. Especially, the active iron species responsible for the decrease of the temperature of transformation to corundum were looked for. To enable the formation of various Fe3+
and Fe2+ species, samples were subjected to thermal treatments in different atmospheres as well as mechanically activated. Thermal analysis and ESR spectroscopy served to follow the processes and to characterise the resulting products. It was found that (i) isolated Fe3+ ions can indicate local structural changes but have (almost) no influence on the temperature of corundum formation, (ii) the temperature of corundum formation decreases in the result of action of small
α-Fe2O3 particles and (iii) during thermal treatments Fe3+ ions are distributed between different phases or precursors thereof: transition aluminas, corundum, Fe2O3, and a Fe3+ pool.
Preparation and properties of sol-gel alumina coatings on metals for high temperature applications
(2012)
Future coal power plants will in case of oxyfuel combustion be operated with altered atmospheres. Hence, corrosion attack might become more severe and steels have to be protected. An alumina-sol was used to coat X20CrMoV12-1 (X20) with alumina to test the protection. Testing was performed at 600 °C in flowing H2O–CO2–O2 and static laboratory air for 1000 h. Oxidation under air is minor compared to exposure in oxyfuel atmosphere. In both cases a multilayered oxide (hematite, magnetite, spinel) was formed on uncoated steels. Carburization appeared on uncoated X20 in H2O–CO2–O2. The coating demonstrates a high protection.
Up to ~ 3 µm thick alumina coatings on corundum ceramic, sodalimesilica glass and Inconel718 were produced from mixtures of boehmite sols and corundum suspensions.
Transmission electron micrographs in combination with electron diffraction and energy dispersive X-ray spectroscopy served to identify crystallographic phases and to characterize the microstructure of the coatings. Using corundum ceramic as substrate the initially deposited boehmite transforms via transition aluminas to corundum while heating to 1200 °C. In the cases of glass and Inconel718 thermal treatments up to 520 °C and 1100 °C, respectively, cause diffusion of ions from the substrates into the coatings. Thus additional oxide phases were formed.
All coatings are free of cracks or delaminations and do not show any directed crystal growth.
Modified Yoldas sols can be used to prepare crack-free well adherent layers on different substrate materials such as sodalime glass, corundum and metal (IN-718). These layers having thicknesses of 0.6 µm are strain tolerant and withstand thermal cycling between 810 °C and room temperature. Introducing alpha-Al2O3 filler particles into modified Yoldas sols allows the preparation of thicker layers of 1.6 µm, which as well can be thermally cycled without noticeable delaminations. Chemical bonding seems to be the predominant layer bonding mechanism.
Aluminas resulting from sols prepared via a modified Yoldas procedure were studied with differential thermal analysis (DTA), differential thermal gravimetrie (DTG), 27Al nuclear magnetic resonance (27Al MAS NMR) and X-ray diffraction (XRD) concerning their thermal properties, aluminum speciation and phase content.
Hydrolysis of aluminum-sec-butoxide in aluminum nitrate solutions allowed to prepare stable sols with varying NO3-/Al molar ratios, solids contents and pH values. Resulting sols contained different aluminum species including also Al13 polycations. Sol preparation conditions also determined aluminum speciation in solid products obtained after thermal treatments of gels obtained from these sols. Al13 polycations and AlO5 species were found to play an important role for thermally induced transformation from amorphous products via eta-Al2O3 to alpha-Al2O3. Intermediately formed eta-Al2O3 promotes the phase transformation to alpha-Al2O3.
Alumina sols were prepared using a modified
Yoldas procedure, thus resulting in sols with high solids
content, excellent long term stability and small particle size.
PH-value ranged between 3.7 and 0.6. Sols were characterised
using rheological, UV-vis transmission and particle
size measurements. Depending on NO3-/Al molar ratio as
well as solids content, sols vary. Analysis of reduced viscosities
indicate the formation of chainlike polymeric species
above a critical solids fraction.
Influence of polyvinylpyrrolidone (PVP) on alumina sols prepared by a modified Yoldas procedure
(2008)
Al13 polycations containing alumina sols, prepared by a modified Yoldas procedure were mixed with polyvinylpyrrolidone (PVP). Although Al speciation in freshly prepared sols was not affected by PVP addition the decay rate of Al13 polycations was slightly decreased in PVP-containing sols. PVP does not show any influence on particle size and particle growth. The influence of PVP addition on viscosity and flow behavior of modified Yoldas sols depends on their solids content and NO3-/Al molar ratio.
Alumina coatings with differing phase compositions were deposited on Inconel-718 (IN-718) Ni-base
superalloy substrates using solgel processing. Mass gain measurements served for studying the oxidation
behavior of coated metal surfaces if exposed to 800°C and 900°C for up to 4000 h in static air. Itwas found, that
alumina coatings significantly reduce the oxidation related mass gain of IN-718 even after heating to 900°C
for 4000 h. Transmission electron microscopy (TEM) studies revealed diffusion of elements from the metal
substrate (IN-718) into the alumina coatings and to a much lower degree from the coating into the
substrate. These diffusion processes are greatly influenced by the phase composition of the coatings, especially
by the presence of alpha-alumina.
Incorporation of a tailor-made size-restricted dithia-aza-oxa macrocycle, 1-oxa-4,10-dithia-7-aza-cyclododecane, via a phenyl linker into two fluorescent sensor molecules with electronically decoupled, rigidly fixed, and sterically preoriented architectures, a 1,3,5-triaryl-2-pyrazoline and a meso-substituted boron-dipyrromethene (BDP), yields amplified fluorescence in the red-visible spectral range upon binding of FeIII ions. The response to FeIII and potentially interfering metal ions is studied in highly polar aprotic and protic solvents for both probes as well as in neat and buffered aqueous solution for one of the sensor molecules, the BDP derivative. In organic solvents, the fluorescence of both indicators is quenched by an intramolecular charge or electron transfer in the excited state and coordination of FeIII leads to a revival of their fluorescence without pronounced spectral shifts. Most remarkably, the unbound BDP derivative shows dual emission in water and can be employed for the selective ratiometric signaling of FeIII in buffered aqueous solutions.
A new method of preparing concentrated alumo-sols, the hydrolysis of Al-tri-sec-butylate in acidic aqueous media at 85°C, was studied in detail by varying the H2O/Al- and NO3 -/Al-ratios in wide ranges. The components of the sols were characterized by 27Al NMR spectroscopy. The pH-value depends on both the chosen H2O/Al- and NO3 -/Al-ratio and on the aging time of the sols and reflects the composition of the sols. Al13 polycations were detected in sols with a pH-value between 3.0 and 3.7. As a new result its presence was shown by NMR below 3.4. The Al13 content of the sols increased with pH and the maximum fraction of Al13 polycations was detected in the sol with the highest pH (3.7). Nearly 65% of the entire aluminium content of this solution is bound in the Al13 polycations. Hence, a new synthetic method for the preparation of Al13 ions containing sols was developed.
Aging studies of the sols showed, that the Al13 polycations were more stable in solutions with higher pH-value. Al13 polycations were detected after an aging time of four months only in sols with a pH-value of 3.7. Tempering the aged sols at 40° to 80°C caused formation of Al13 and also of Al30 polycations.
Zn-K transmission EXAFS measurements were performed on vitrified ashes from municipal waste incinerator facilities, which contain low amounts of Zn (up to 3 wt%) and sulphur (up to 0.5 wt%) in a ZnS phase. From the Fourier transform it can be concluded that the zinc ions are fourfold co-ordinated by oxygen or sulphur ions. The amount of zinc ions of sulphur environment, e.g. the concentration of ZnS, was determined by Fourier filtering and subsequent parameter fitting. A quantitative analysis of low ZnS concentrations up to 1 wt% has been performed for samples with a molar ratio Zn/S < 5.
Alumosols in combination with well dispersed corundum were successfully used to form up to 2.5 ìm thick coatings on the Ni-base alloy SC16. These coatings withstood heat treatments at 700 °C in a water vapour containing atmosphere. The heat treatment caused formation of delta-alumina in the coating and diffusion of chromium and titanium into the coating.