Ionenstrahlbasierte Oberflächenmodifizierung von TiAl-Werkstoffen

Abstract des Vortrages: Titanium aluminide (TiAl) alloys are attractive lightweight materials for mediumtemperature (500°-750°C) structural applications including components such as jet engine and industrial gas turbine blades, turbocharger rotors and automotive engine valves. However, envisaged service temperatures for future advanced applications will have to be in the range of 750° to 1000°C, over which these alloys suffer from both oxidation and oxygen embrittlement. Therefore, development of surfaceengineering techniques for preventing high-temperature environmental damage is critical in exploiting the advantages of TiAl alloys to their fullest extent. Two efficient approaches to protecting candidate TiAl alloys from high-temperature (>750°C) environmental degradation have been developed at HZDR. The first technique involves a single step, namely treating TiAl alloy components directly by plasma immersion ion implantation (PIII) of fluorine using a mixture of difluoromethane and argon (CH2F2 + 25% Ar) as the precursor gas. The oxidation performance of the fluorine-implanted alloys has been evaluated by thermal gravimetric analysis (TGA) over the temperature range of 750° to 1050°C under conditions of both isothermal and thermal cyclic oxidation in air, and for times as long as 6000 h. This type of surface modification has been shown to produce a stable, adherent and highly protective alumina scale. The second technique involves the fabrication of a durable protective coating in a two-step process, namely formation of a thin aluminum-rich TiAl layer (Ti-60Al) by chemical vapor deposition (CVD) employing a mixture of inorganic precursors, followed by PIII of fluorine. Subsequent long-term oxidation exposures to air at 900°C of a GE 4822 alloy (Ti-48Al-2Cr-2Nb; alloy composition qualified for aerospace applications) have shown that the coating so developed is able to successfully prevent oxidation damage to the base material while maintaining up to 90% of its initial mechanical properties (strength and ductility)

Fluor-schorl, a new member of the tourmaline supergroup, and new data on schorl from the cotype localities

Fluor-schorl, NaFe^(2+) _3Al_6Si_6O_(18)(BO_3)_3(OH)_3F, is a new mineral species of the tourmaline supergroup from alluvial tin deposits near Steinberg, Zschorlau, Erzgebirge (Saxonian Ore Mountains), Saxony, Germany, and from pegmatites near Grasstein (area from Mittewald to Sachsenklemme), Trentino, South Tyrol, Italy. Fluor-schorl was formed as a pneumatolytic phase and in high-temperature hydrothermal veins in granitic pegmatites. Crystals are black (pale brownish to pale greyish-bluish, if distance (r^2 = 0.93). This correlation indicates that Fe^(2+)-rich tourmalines from the investigated localities clearly tend to have a F-rich or F-dominant composition. A further strong positive correlation (r^2 = 0.82) exists between the refined F content and the Y–W (F,OH) distance, and the latter may be used to quickly estimate the F content

The MoS2 Nanotubes with Defect-Controlled Electric Properties

We describe a two-step synthesis of pure multiwall MoS2 nanotubes with a high degree of homogeneity in size. The Mo6S4I6 nanowires grown directly from elements under temperature gradient conditions in hedgehog-like assemblies were used as precursor material. Transformation in argon-H2S/H2 mixture leads to the MoS2 nanotubes still grouped in hedgehog-like morphology. The described method enables a large-scale production of MoS2 nanotubes and their size control. X-ray diffraction, optical absorption and Raman spectroscopy, scanning electron microscopy with wave dispersive analysis, and transmission electron microscopy were used to characterize the starting Mo6S4I6 nanowires and the MoS2 nanotubes. The unit cell parameters of the Mo6S4I6 phase are proposed. Blue shift in optical absorbance and metallic behavior of MoS2 nanotubes in two-probe measurement are explained by a high defect concentration

Spin-dependent transport in nanocomposite C:Co films

The magneto-transport properties of nanocomposite C:Co (15 and 40 at.% Co) thin films are investigated. The films were grown by ion beam co-sputtering on thermally oxidized silicon substrates in the temperature range from 200 to 500 degC. Two major effects are reported: (i) a large anomalous Hall effect amounting to 2 \mu ohm cm, and (ii) a negative magnetoresistance. Both the field-dependent resistivity and Hall resistivity curves coincide with the rescaled magnetization curves, a finding that is consistent with spin-dependent transport. These findings suggest that C:Co nanocomposites are promising candidates for carbon-based Hall sensors and spintronic devices.Comment: 13 pages, 7 figure

Limitations of Fe^(2+) and Mn^(2+) site occupancy in tourmaline: Evidence from Fe^(2+)- and Mn^(2+)-rich tourmaline

Fe^(2+)- and Mn^(2+)-rich tourmalines were used to test whether Fe^(2+) and Mn^(2+) substitute on the Z site of tourmaline to a detectable degree. Fe-rich tourmaline from a pegmatite from Lower Austria was characterized by crystal-structure refinement, chemical analyses, and Mössbauer and optical spectroscopy. The sample has large amounts of Fe^(2+) (~2.3 apfu), and substantial amounts of Fe^(3+) (~1.0 apfu). On basis of the collected data, the structural refinement and the spectroscopic data, an initial formula was determined by assigning the entire amount of Fe^(3+) (no delocalized electrons) and Ti^(4+) to the Z site and the amount of Fe^(2+) and Fe^(3+) from delocalized electrons to the Y-Z ED doublet (delocalized electrons between Y-Z and Y-Y): X(Na_(0.9)Ca_(0.1)) ^Y(Fe^(2+)_(2.0)Al_(0.4)Mn^(2+)_(0.3)Fe^(3+)_(0.2)) ^Z(Al_(4.8)Fe^(3+)_(0.8)Fe^(2+)_(0.2)Ti^(4+)_(0.1)) ^T(Si_(5.9)Al_(0.1))O_(18) (BO_3)_3^V(OH)_3 ^W[O_(0.5)F_(0.3)(OH)_(0.2)] with α = 16.039(1) and c = 7.254(1) Å. This formula is consistent with lack of Fe^(2+) at the Z site, apart from that occupancy connected with delocalization of a hopping electron. The formula was further modified by considering two ED doublets to yield: ^X(Na_(0.9)Ca_(0.1)) ^Y(Fe^(2+)_(1.8)Al_(0.5)Mn^(2+)_(0.3)Fe^(3+)_(0.3)) ^Z(Al_(4.8)Fe^(3+)_(0.7)Fe^(2+)_(0.4)Ti^(4+)_(0.1)) ^T(Si_(5.9_Al_(0.1))O_(18) (BO_3)_3 ^V(OH)_3 ^W[O_(0.5)F_(0.3)(OH)_(0.2)]. This formula requires some Fe^(2+) (~0.3 apfu) at the Z site, apart from that connected with delocalization of a hopping electron. Optical spectra were recorded from this sample as well as from two other Fe^(2+)-rich tourmalines to determine if there is any evidence for Fe^(2+) at Y and Z sites. If Fe^(2+) were to occupy two different 6-coordinated sites in significant amounts and if these polyhedra have different geometries or metal-oxygen distances, bands from each site should be observed. However, even in high-quality spectra we see no evidence for such a doubling of the bands. We conclude that there is no ultimate proof for Fe^(2+) at the Z site, apart from that occupancy connected with delocalization of hopping electrons involving Fe cations at the Y and Z sites. A very Mn-rich tourmaline from a pegmatite on Elba Island, Italy, was characterized by crystal-structure determination, chemical analyses, and optical spectroscopy. The optimized structural formula is ^X(Na_(0.6)□_(0.4)) ^Y(Mn^(2+)_(1.3)Al_(1.2)Li_(0.5)) ^ZAl_6 ^TSi_6O_(18) (BO_3)_3 ^V(OH)_3 ^W[F_(0.5)O_(0.5)], with α = 15.951(2) and c = 7.138(1) Å. Within a 3σ error there is no evidence for Mn occupancy at the Z site by refinement of Al ↔ Mn, and, thus, no final proof for Mn^(2+) at the Z site, either. Oxidation of these tourmalines at 700–750 °C and 1 bar for 10–72 h converted Fe^(2+) to Fe^(3+) and Mn^(2+) to Mn^(3+) with concomitant exchange with Al of the Z site. The refined ^ZFe content in the Fe-rich tourmaline increased by ~40% relative to its initial occupancy. The refined YFe content was smaller and the distance was significantly reduced relative to the unoxidized sample. A similar effect was observed for the oxidized Mn^(2+)-rich tourmaline. Simultaneously, H and F were expelled from both samples as indicated by structural refinements, and H expulsion was indicated by infrared spectroscopy. The final species after oxidizing the Fe^(2+)-rich tourmaline is buergerite. Its color had changed from blackish to brown-red. After oxidizing the Mn^(2+)-rich tourmaline, the previously dark yellow sample was very dark brown-red, as expected for the oxidation of Mn^(2+) to Mn^(3+). The unit-cell parameter α decreased during oxidation whereas the c parameter showed a slight increase

Ion Beam Synthesis of Cobalt Silicide Layers in Si(111)

Thin CoSi2 layers are formed by 195 keV Co ion implantation in Si(111) substrates to a dose of 2 × 1017 Co+/cm2 at room temperature (RT) followed by annealing in N2 atmosphere at different temperatures during 1 h are investigated. The characterizations of the as-implanted and annealed samples are performed using Rutherford backscattering spectrometry (RBS) and X-ray diffraction (XRD). Also the obtained samples have been characterized by means of Raman spectroscopy. The results show that the CoSi2 phase is polycrystalline with a random crystallographic orientation

Ionenstrahlbasierte Oberflächenmodifizierung von TiAl-Werkstoffen

Abstract des Vortrages: Titanium aluminide (TiAl) alloys are attractive lightweight materials for mediumtemperature (500°-750°C) structural applications including components such as jet engine and industrial gas turbine blades, turbocharger rotors and automotive engine valves. However, envisaged service temperatures for future advanced applications will have to be in the range of 750° to 1000°C, over which these alloys suffer from both oxidation and oxygen embrittlement. Therefore, development of surfaceengineering techniques for preventing high-temperature environmental damage is critical in exploiting the advantages of TiAl alloys to their fullest extent. Two efficient approaches to protecting candidate TiAl alloys from high-temperature (>750°C) environmental degradation have been developed at HZDR. The first technique involves a single step, namely treating TiAl alloy components directly by plasma immersion ion implantation (PIII) of fluorine using a mixture of difluoromethane and argon (CH2F2 + 25% Ar) as the precursor gas. The oxidation performance of the fluorine-implanted alloys has been evaluated by thermal gravimetric analysis (TGA) over the temperature range of 750° to 1050°C under conditions of both isothermal and thermal cyclic oxidation in air, and for times as long as 6000 h. This type of surface modification has been shown to produce a stable, adherent and highly protective alumina scale. The second technique involves the fabrication of a durable protective coating in a two-step process, namely formation of a thin aluminum-rich TiAl layer (Ti-60Al) by chemical vapor deposition (CVD) employing a mixture of inorganic precursors, followed by PIII of fluorine. Subsequent long-term oxidation exposures to air at 900°C of a GE 4822 alloy (Ti-48Al-2Cr-2Nb; alloy composition qualified for aerospace applications) have shown that the coating so developed is able to successfully prevent oxidation damage to the base material while maintaining up to 90% of its initial mechanical properties (strength and ductility)

Ionenstrahlbasierte Oberflächenmodifizierung von TiAl-Werkstoffen

Abstract des Vortrages: Titanium aluminide (TiAl) alloys are attractive lightweight materials for mediumtemperature (500°-750°C) structural applications including components such as jet engine and industrial gas turbine blades, turbocharger rotors and automotive engine valves. However, envisaged service temperatures for future advanced applications will have to be in the range of 750° to 1000°C, over which these alloys suffer from both oxidation and oxygen embrittlement. Therefore, development of surfaceengineering techniques for preventing high-temperature environmental damage is critical in exploiting the advantages of TiAl alloys to their fullest extent. Two efficient approaches to protecting candidate TiAl alloys from high-temperature (>750°C) environmental degradation have been developed at HZDR. The first technique involves a single step, namely treating TiAl alloy components directly by plasma immersion ion implantation (PIII) of fluorine using a mixture of difluoromethane and argon (CH2F2 + 25% Ar) as the precursor gas. The oxidation performance of the fluorine-implanted alloys has been evaluated by thermal gravimetric analysis (TGA) over the temperature range of 750° to 1050°C under conditions of both isothermal and thermal cyclic oxidation in air, and for times as long as 6000 h. This type of surface modification has been shown to produce a stable, adherent and highly protective alumina scale. The second technique involves the fabrication of a durable protective coating in a two-step process, namely formation of a thin aluminum-rich TiAl layer (Ti-60Al) by chemical vapor deposition (CVD) employing a mixture of inorganic precursors, followed by PIII of fluorine. Subsequent long-term oxidation exposures to air at 900°C of a GE 4822 alloy (Ti-48Al-2Cr-2Nb; alloy composition qualified for aerospace applications) have shown that the coating so developed is able to successfully prevent oxidation damage to the base material while maintaining up to 90% of its initial mechanical properties (strength and ductility)