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  • 1
    Monograph available for loan
    Monograph available for loan
    Brussel : Commission of the European Communities
    Call number: PIK N 076-01-0147
    Type of Medium: Monograph available for loan
    Pages: 453 p.
    ISBN: 2872630317
    Series Statement: Water Pollution Research Report 13
    Location: A 18 - must be ordered
    Branch Library: PIK Library
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 30 (1958), S. 1005-1006 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 26 (1954), S. 1886-1889 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 43 (1987), S. 927-928 
    ISSN: 1420-9071
    Keywords: Purkinje cells ; cerebellar ontogeny ; giant mitochondria ; reptiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Giant mitochondria were observed in the perikarya and dendrites of Purkinje cells in the developing cerebellar cortex of the lizardGallotia galloti at sevral stages previous to hatching. Such mitochondria are absent from the adult cerebellum.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1866
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The strata-bound fluorite-(barite-)Pb-Zn ore deposits occurring within the more than 3,000 m thick Alpujárride Carbonate Formation of the Betic Cordillera, southern Spain, are linked to two defined stratigraphic positions (within the Anisian and at the Ladinian-Carnian transition) and to definite sedimentary contexts. These are highly restricted lagoons isolated from the open sea by calcarenitic barriers with noticeable development of algal mats in their inner margins. Preevaporitic deposition conditions are usually recognized. The ore-bearing horizons are located either at the transition from evaporitic to normal marine deposition (as in the case of the Anisian ore-bearing horizon) or at the transition from normal marine to evaporite deposition (as in the case of the uppermost Ladinian to lowermost Carnian ore-bearing horizon). These vertical facies changes correspond also to the transitions from predominantly terrigenous (continental and/or coastal) sedimentation to marine carbonate sedimentation (Anisian ore deposits) and vice versa (upper Ladinian-lower Carnian). It is proposed that the ore deposits in the Triassic Alpujárride Formation are controlled by certain facies associations in the lagoonal environment. The depositional environment determines the hydrologic regimes responsible for early diagenetic formation of fluorite and of the related ore minerals in a way similar to that of early-diagenetic dolomite. This hypothesis is consistent with field and petrographic observations and with available geochemical and itotopic data reported in other works. The present investigation intends to underline the role played by surface-linked ore formation processes, i.e., by ore-forming processes essentially linked to the environments in which sedimentation and early diagenesis takes place, in the genesis of numerous strata-bound Zn-Pb-(F-Ba) ore deposits in carbonate rocks.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 57 (1996), S. 532 -535 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 4425-4426 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dissociation energy of boron hydride has been calculated ab initio using a very accurate theoretical model, with an expected accuracy of ±0.2 kcal mol−1. The values of 85.7 and 82.4 kcal mol−1 for De and D0, respectively, confirm the conclusion of Curtiss and Pople [J. Chem. Phys. 90, 2522 (1989)], that the predissociation limit of 82.6±0.4 kcal mol−1 might be close to the actual dissociation energy, and that an earlier proposed De of 78.9 kcal mol−1 is in error.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6655-6667 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The spectroscopic properties of the three lowest-lying states X 3Π, A 3∑−, and a 1∑+ of SiC have been computed accurately using augmented coupled cluster methods and different basis sets. Partition functions have been set up, accounting for anharmonicity, rotation–vibration coupling, centrifugal distortion, and isotope effects. Thermodynamic properties are tabulated in JANAF style from 100 to 6000 K. A critical analysis of the effects of the various contributions is made, as well as an error analysis.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 6469-6485 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: For a number of different structures and states of B3, B2N, BN2, and N3, optimum geometries and harmonic spectra were obtained at the HF/6-31G* level. The relative stability of the isomers was determined using full fourth-order Møller–Plesset theory, both with and without spin projection, as well as coupled cluster methods. Estimates for the dissociation energies are based on scaled CCD+ST(CCD) binding energies. Koopmans' vertical ionization potentials and Mulliken charge distributions, both at the UHF/6-31G* level, are quoted for the most stable isomers. B3 is found to be an equilateral triangle in its 2A'1 ground state. B2N has a symmetric linear arrangement in its 2Σ+u ground state with an extremely low bending frequency (73 cm−1), and an unusually low vertical ionization potential (6.75 eV). Its asymmetric stretching (2021 cm−1) is found to be extremely intense (8782 km mol−1). BN2 has four rather closely spaced states, of which an isosceles triangle is the absolute minimum (2A1 state). However, at high temperatures, an asymmetric linear arrangement (2Π state) is found to have equal importance, whereas a 4Σ− state plays a role there too. The same theoretical methods correctly predict for N3 a symmetric linear arrangement in the 2Πg ground state; the spectroscopic constants are found to be in reasonable agreement with experiment. Estimated dissociation energies (expected accuracy ±4 kcal mol−1) are: B3 197.9, B2N 265.0, BN2 224.9, N3 210.1 kcal mol−1. From a statistical thermodynamical analysis, B3 is stable against dissociation to B2 and B up to very high temperatures, B2N is extraordinarily stable, whereas BN2 and N3 dissociate spontaneously to B+N2 and N+N2 at all temperatures. From these results, the presence of B2N+ and B+3, the high abundance of B2N+, as well as the absence of BN+2 and N+3 in laser mass spectra of boron nitride is explained.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 7633-7645 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The anharmonic potential energy surface of water has been computed ab initio using an augmented coupled cluster method and various basis sets. Whereas the Pople 6–311 G family is manifestly unsatisfactory, Huzinaga–Dunning basis sets perform quite well. The [5s4p2d1f,3s2p] surface reproduces harmonic frequencies and anharmonicity constants to better than about 2 and 1 cm−1, respectively. For quantitative agreement with experiment, both f functions on oxygen and inclusion of core correlation seem to be prerequisite. Comparison with various experimentally derived force fields reveals that the ab initio force field is of comparable quality. From the best computed force field, a set of spectroscopic constants has been derived for all important isotopomers of water. Using a hybrid analytic/direct summation method recently developed by the present authors, the thermodynamic functions gef(T), hcf(T), S0, and Cp are computed including exact account of anharmonicity and rovibrational coupling, and very good analytical approximations to centrifugal distortion and quantum rotation effects. The computed functions substantially revise previous literature results at high temperatures. Differences between thermodynamic functions from various computed force fields are an order of magnitude smaller than these errors. Thermodynamic tables in JANAF style from 100 to 3000 K, as well as a full set of rovibrational spectroscopic constants, are presented. It is concluded that obtaining force fields of near-spectroscopic accuracy, and thermodynamic tables of very high accuracy, is presently feasible for small polyatomic molecules.
    Type of Medium: Electronic Resource
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