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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Accreditation and quality assurance 2 (1997), S. 130-136 
    ISSN: 1432-0517
    Keywords: Key words Reference material ; Standard gas ; Standard solution ; Traceability ; Measurement Law
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract  Analytical instruments used for measurements of air and water pollution are calibrated by using reference materials such as standard gases and standard solutions. In Japan, since the middle of the 1970s, those reference materials which are traceable to the national standards maintained at national research institutes have been supplied to users by reference material producers. In order to establish the primary standards and to secure the traceability from the working standards to the national ones, various analytical methods such as coulometric, titrimetric and gravimetric analyses for purity determination and highly sensitive atomic spectrometry for trace analysis have been developed as the primary methods and reference methods. The Japanese Measurement Law, revised in 1992, has introduced a new traceability system in which a public organization, a "designated calibration body", can also prepare and maintain the national standards under the advice and instruction of national research institutes. The designated calibration body can provide calibration services to reference material producers (accredited calibration bodies) by using the national standards. The reference materials supplied in conformity with the traceability system include standard gases, pH standard solutions, metal standard solutions and non-metal ion standard solutions.
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    Journal of Mathematical Physics 36 (1995), S. 4571-4589 
    ISSN: 1089-7658
    Source: AIP Digital Archive
    Topics: Mathematics , Physics
    Notes: In the Fock–Bargmann space, the complete harmonic-oscillator basis for the three-cluster system is constructed. The indices of the reduction U(6)&supuline;U(2)×U(3) are chosen as the quantum numbers. The Pauli-forbidden states are eliminated by the orthogonal transformation of basis functions. The basis states are obtained in terms of hypergeometric functions and the spherical Wigner functions. Their simple form allows one to solve the problem of calculating the matrix elements of the microscopic Hamiltonian needed for the study of three-cluster systems within the algebraic version of RGM. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant breeding 118 (1999), S. 0 
    ISSN: 1439-0523
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: A homoeologous quantitative trait locus to that of eps5L on barley chromosome 5H was identified in a syntenic region of wheat chromosome 5A. Wheat single chromosome recombinant lines (SCRs) were developed from a cross between ‘Chinese Spring’(‘Cappelle-Desprez’ 5A) and ‘Chinese Spring’(Triticum spelta 5A), these were grown together with the parental controls under different vernalization and photoperiod regimes. The variation for ear emergence time accelerated heading induced by the T. spelta segment indicated an effect associated with the Xcdo412-Xbcd9 interval. Since no differences between the SCRs and controls in responses to vernalization and photoperiod treatments were detected, this effect was identified as an earliness per se gene, Q Eetocs-5 A.2, which may be homoeologous to the eps5L quantitative trait locus of barley. Xbcd926 has been found to be closely linked to the rice flowering time quantitative trait loci, QHd9a or FLTQ2, on chromosome 9, suggesting possible relationships among the quantitative trait loci across wheat, barley and rice genomes.
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 80 (1996), S. 6097-6098 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: LiClO4⋅3H2O has been found to be 90° phase-matchable for ultraviolet generation at 0.2660 μm at a crystal temperature of 30.6 °C. A peak power as high as 28 MW with an average power of 2.2 W was obtained in a 1.5-cm-long crystal. Sellmeier's equations and nonlinear constant of this crystal are reported. © 1996 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 52 (1996), S. 2836-2837 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 6
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 52 (1996), S. 303-313 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The complex (2-cyanoethyl)bis(dimethylglyoximato)(triphenylphosphine)cobalt(III), [Co(C4H7N2O2)2(C3H4N){P(C6H5)3}], when it was crystallized rapidly from an aqueous methanol solution, has four crystal forms, three of which were obtained separately from different solvents in large amounts. The crystal structures of the four forms were determined by X-rays. The molecular structures in the four forms have different conformations around the Co—C and Co—P bonds. The packing energy calculation indicated that the four forms have approximately the same energy. The 2-cyanoethyl group of this complex was isomerized to the 1-cyanoethyl group when the powdered sample of the complex was irradiated with a xenon lamp. For three crystal forms prepared separately, the solid-state photoisomerization rates were measured from the change in the IR spectra, assuming first-order kinetics. A quantitative relationship between the rate constant and the size of the reaction cavity for the 2-cyanoethyl group has been obtained for the three crystal forms.
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  • 7
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 599-603 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The unit cell and space group of orthorhombic NaV6O11 (low-temperature form) are found by an X-ray single-crystal diffraction study at 300 K (hexagonal, P63/mmc), 100 K (hexagonal, P63mc) and 20 K (orthorhombic). The orthorhombic form (o) shows no superstructure and its unit cell is related to the hexagonal one (h): ao ∼ ah + bh, ao ∼ −ah + bh and co ∼ ch. Bijvoet-pair examination confirms that it crystallizes in the noncentrosymmetric space group Cmc21. The hexagonal (P63mc)-orthorhombic (Cmc21) structural phase transition is proved to be of second order.
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  • 8
    Electronic Resource
    Electronic Resource
    Chester : International Union of Crystallography (IUCr)
    Journal of synchrotron radiation 5 (1998), S. 1004-1006 
    ISSN: 1600-5775
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The results of Br K-edge X-ray absorption measurements of 1-bromonaphthalene dissolved in supercritical fluid Xe are reported. As the pressure of Xe confined in a high-pressure cell is increased, the absorption spectrum of bromonaphthalene gradually appears, showing that Xe in the supercritical fluid state solvates the bromonaphthalene molecule. The spectrum of the dissolved sample shows a remarkable difference from that of the pure liquid sample in the near-edge region of the X-ray absorption spectrum, reflecting the interaction of the solute material with solvent Xe. Ab initio full multiple-scattering calculations can reproduce the spectral features qualitatively. A large value of the Debye–Waller factor must be introduced to give the best fit, corresponding to a large degree of spatial disorder and violent thermal vibration of the Xe atoms around the Br atom.
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  • 9
    ISSN: 1573-482X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Precursors for layer-structured perovskite thin films of Sr2Bi2Ta3O12.5 or SBT223, and Sr2Bi2Nb3O12.5 or SBN223 were prepared by the reactions of Sr-Bi (2 : 2) double methoxyethoxide and Ta or Nb methoxyethoxide, followed by partial hydrolysis. By several analytical techniques, such as 1H-, 13C- and 93Nb-NMR (nuclear magnetic resonance) and FT-IR (Fourier transform infrared) the molecular structure of the precursors was found to be similar to the layer-structured perovskite crystal sub-lattice. As a result, the onset of crystallization in the sol-gel derived SBT223 thin films was at a low temperature of 550°C. By rapid thermal annealing in an oxygen atmosphere, the single-phase perovskite films exhibited preferred (1 1 7) orientation. In contrast to the SBT system, the observed number of the pseudo-perovskite layers of TaO6 octahedral units between Bi2O 2 2 + layers in the SBT223 was three. Despite the elongation of the unit cell along the c-axis, 700°C-heated SBT223 thin film did not exhibit a saturated hysteresis loop due to the small crystallite size.
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  • 10
    ISSN: 1432-0827
    Keywords: Fluoride ; Bone ; Defluoridation ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Abstract The aim of this work was to explore the reduction of fluoride concentrations in the skeleton after stopping experimental fluoride administration. Fluoride was administered to the rats at varying doses (0, 50, 100 ppm in drinking water) and for different lengths of time (4, 13, 25 weeks). A series of fluoride concentrations across the full thickness of humerus, parietal bone, and vertebra arch in rats were measured by means of an abrasive micro-sampling technique. The distribution profiles of fluoride from periosteal to endosteal surfaces, which were apparently related to the histological structure of these bones, were U shaped in the humerus, V shaped in the parietal bone, and W shaped in the vertebra arch. The average fluoride concentrations in the bones increased significantly with each increasing dose and length of fluoride administration. The relative increments were similar between the different regions or the different bones. After stopping fluoride administration, on the other hand, the relative reduction of the average fluoride concentrations in the bones were 30–100%. They were greatly related to the length after stopping fluoride administration and the dose and length of fluoride administration, but also dependent upon the type of bone and the region examined.
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