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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 2327-2331 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Silicon dioxide was deposited on a Pt/Pb(ZrxTi1−x)O3/Pt capacitor by the plasma-enhanced chemical-vapor deposition (PECVD) method. We have been investigated the mechanism of blister formation on the PECVD SiO2/Pt/PZT/Pt capacitor. The blisters were observed at the temperature of 325 °C in O2 atmosphere, while in N2 and Ar atmosphere blisters were not formed even at 500 °C. Hydrogen evolution analysis from the PECVD SiO2 layer showed a sharp peak near 320 °C. The results indicated that the accumulation of water-vapor pressure developed by chemical reaction between oxygen and hydrogen could be the dominant mechanism of blister formation in PECVD SiO2/Pt/PZT/Pt capacitors. © 2001 American Institute of Physics.
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 86 (1999), S. 6376-6381 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A wet cleaning solution was designed to specifically eliminate nonferroelectric phases, such as pyrochlore, PbO, and the etching damaged layer. Scanning electron microscopy pictures clearly showed that treatment with the cleaning solution completely removed these nonferroelectric phases. After removing the nonferroelectric phases, ferroelectric properties such as remnant polarization, coercive voltage, and leakage current, were remarkably improved. In addition, the wet cleaned ferroelectric capacitors yielded superior endurance against hydrogen-induced damage compared to those of the noncleaned capacitors. © 1999 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 75 (1999), S. 3811-3813 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Considerable increase in compressive stress was observed in silicon dioxide films upon prolonged exposure to atmospheric moisture. The compressive stress change upon exposure to atmosphere consisted of a reversible change and an irreversible change. The irreversible component was found to be due to structural changes in the Si–O–Si network. The reversible change in stress is due to water molecules absorbed on walls of the pores. © 1999 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Reactions between SiC and mullite in an Ar plasma were investigated using a model composite in which a free-standing CVD SiC coupon was imbedded in mullite cement. After treatment in a radio frequency (RF) plasma, the Si content of the mullite in contact with SiC was found to be less than that in the starting material, and deposits were found on the walls of the plasma chamber due to the reaction of mullite with SiC as follows: Al6Si2O13(s)+ SiC(s)= 3Al2O3(s)+ 3SiO(g)+ CO(g). This reaction, which is endothermic (1405 kJ/mol at 1500 K), absorbs thermal energy and consequently prevents the rapid sintering which is observed for single-phase mullite in similar environments. As a consequence, it is suggested that RF plasma sintering probably cannot be used to densify SiC-reinforced mullite-matrix composites because of the resulting energy consumption and damage to the SiC phase.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 51 (1999), S. 383-402 
    ISSN: 1573-4889
    Keywords: TITANIUM ; TANTALUM ; TITANIUM-TANTALUM ALLOYS ; OXIDATION MECHANISM ; OXIDATION KINETICS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation behavior of titanium-tantalumalloys was investigated with respective concentrationsof each element ranging from 0 to 100 wt.%. Alloys wereexposed to argon-20% oxygen at 800 to 1400°C. Theslowest oxidation rates were observed in alloys with5-20% Ta. The oxidation kinetics of alloys containingless than approximately 40% Ta were approximatelyparabolic. Pure Ta exhibited nearly linear kinetics. Alloys containing 50% or more Taexhibited paralinear kinetics. The activation energiesfor oxidation ranged between 232 kJ/mole for pure Ti and119 kJ/mole for pure Ta, with the activation energies of the alloys falling between these values andgenerally decreasing with increasing Ta content. Theactivation energies for oxidation of the end members, Tiand Ta, agree well with published values for the activation energies for diffusion of oxygenin α-Ti and Ta. Scale formation in the alloys wasfound to be complex exhibiting various layers of Ti-,Ta-, and TiTa-oxides. The outermost layer of the oxidized alloys was predominately rutile(TiO2). Beneath the TiO2 grew avariety of other oxides with the Ta content generallyincreasing with proximity to the metal-oxide interface.It was found that the most oxidation-resistant alloys hadcompositions falling between Ti5Ta andTi-15Ta. Although Ta stabilizes the β-phase of Ti,the kinetics of oxidation appeared to be rate limited byoxygen transport through the oxygen-stabilized α-phase.However, the kinetics are complicated by the formationof a complex oxide, which cracks periodically. Tantalumappears to increase the compositional range ofoxygen-stabilized α-phase and reduces both the solubilityof oxygen and diffusivity of Ti in the α- andβ-phases.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 807-815 
    ISSN: 0887-6266
    Keywords: moisture effect ; glass transition ; low temperature relaxations ; semiaromatic amorphous polyamides ; hydrogen bonding ; molecular analysis ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of moisture absorption on the primary (glass) transition (Ta or Tg) and the low temperature relaxations of semiaromatic amorphous polyamides synthesized by isomeric aliphatic diamine and metha or para oriented phthalicdiacids has been investigated by means of differential scanning calorimeter (DSC) and dynamic mechanical thermal analyser (DMTA). The glass transition of semiaromatic polyamides was lowered due to the water absorption, and the β and the γ relaxations were as well. From the observed Tg and the difference in the heat capacity, the calculated Tg depression per 1 wt % water content was 12.3 K and the result was in good agreement with the experimental data. The depression of the glass transition may be expressed by the same manner as the plasticization of nylon 6 by water. The depressed β relaxation observed in the specimen containing a few percent of moisture was splitted into two transitions due to the reduction of water content, of which one was the elevation of the Tβ and another was the simultaneous appearance of the Tγ, and then the single Tγ solely was observed for the completely dried specimen. The Tγ seemed to be merged into or not to be observed by the large and broad Tβ transition when the sample was governed by a few percent of water, then it was emerged from the Tβ due to water desorption. Thus, the Tβ is believed to arise from the intermolecular hydrogen bonding between water molecules or between water and amide groups in wet polyamides. In addition, the γ relaxation originated from the peptide groups is attributable to the inter- and intramolecular hydrogen bonding between amide groups. © 1997 John Wiley & Sons, Inc. J Polyn Sci B: Polym Phys 35: 807-815, 1997
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1981-1986 
    ISSN: 0887-6266
    Keywords: polystyrene ; poly(2,6-dimethyl-1,4-phenylene oxide) ; blend ; molecular relaxation ; low temperature relaxations ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular relaxation behavior in terms of the α, β, and γ transitions of miscible PS/PPO blends has been studied by means of DMTA and preliminary work has been carried out using DSC. From DSC and DMTA (by tan δ), the observed α relaxation (Tα or Tg) of PS, PPO, and the blends, which are intermediate between the constituents, are in good agreement with earlier reports by others. In addition, the β transition (Tβ) of PS at 0.03 Hz and 1 Hz is observed at -30 and 20°C, respectively, while the γ relaxation (Tγ) is not observed at either frequency. The Tβ of PPO is 30°C at 0.03 Hz and is not observed at 1 Hz, while the Tγ is -85°C at 0.03 Hz and -70°C at 1 Hz. On the other hand, blend composition-independent β or γ relaxation observed in the blends may be a consequence of the absence of intra- or intermolecular interaction between the constituents at low temperature. Thus it is suggested that at low temperature, the β relaxation of PS be influenced solely by the local motion of the phenylene ring, and that the β or γ relaxation of PPO be predominated by the local cooperative motions of several monomer units or the rotational motion of the methyl group in PPO. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1981-1986, 1998
    Additional Material: 6 Ill.
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  • 8
    Publication Date: 2016-03-28
    Print ISSN: 2470-0010
    Electronic ISSN: 2470-0029
    Topics: Physics
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  • 9
    Publication Date: 2020-09-01
    Description: We propose a new intuitive metric for evaluating the tension between two experiments, and apply it to several data sets. While our metric is non-optimal, if evidence of tension is detected, this evidence is robust and easy to interpret. Assuming a flat ΛCDM cosmological model, we find that there is a modest 2.2σ tension between the DES Year 1 results and the Planck measurements of the Cosmic Microwave Background (CMB). This tension is driven by the difference between the amount of structure observed in the late-time Universe and that predicted from fitting the Planck data, and appears to be unrelated to the tension between Planck and local estimates of the Hubble rate. In particular, combining DES, Baryon Acoustic Oscillations (BAO), Big-Bang Nucleosynthesis (BBN), and supernovae (SNe) measurements recovers a Hubble constant and sound horizon consistent with Planck, and in tension with local distance-ladder measurements. If the tension between these various data sets persists, it is likely that reconciling all current data will require breaking the flat ΛCDM model in at least two different ways: one involving new physics in the early Universe, and one involving new late-time Universe physics.
    Print ISSN: 0035-8711
    Electronic ISSN: 1365-2966
    Topics: Physics
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  • 10
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