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  • 1
    Electronic Resource
    Electronic Resource
    Phase relations in the Fe-Ni-Cr-S system and the sulfidation of an austenitic stainless steel (1979)
    Springer
    Oxidation of metals 13 (1979), S. 25-55 
    Details
    ISSN: 1573-4889
    Keywords: thermochemical diagrams ; Fe-Cr-S system ; Fe-Ni-S system ; Ni-Cr-S system ; Fe-Ni-Cr-S system
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The stability fields of various sulfide phases that form on Fe-Cr, Fe-Ni, Ni-Cr, and Fe-Cr-Ni alloys have been developed as a function of temperature and the partial pressure of sulfur. The calculated stability fields in the ternary A-B-S system are displayed on plots of log $${\text{p}}_{S_2 } $$ vs. the conjugate extensive variable (nA/nA−nB), which provides a better framework for following the sulfidation of Fe-Cr-Ni alloys at high temperatures. Experimental and estimated thermodynamic data were used in developing the sulfur potential diagrams. Current models and correlations were employed to estimate the unknown thermodynamic behavior of solid solutions of sulfides and to supplement the incomplete phase-diagram data of geophysical literature. These constructed stability field diagrams are in excellent agreement with the sulfide phases and compositions determined experimentally during the sulfidation of SAE 310 stainless steel. The sulfur potential plots appear to be very useful in predicting and correlating the sulfidation of commercial alloys.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00715869
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  • 2
    Electronic Resource
    Electronic Resource
    T-maze phototaxis ofDrosophila melanogaster and several mutants in the visual systems (1977)
    Springer
    Journal of comparative physiology 116 (1977), S. 209-225 
    Details
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary T-maze phototaxis ofDrosophila melanogaster and several of its mutants was investigated as function of the light illuminating the mazes. For visible light the response curves of thewildtype are quite complex and nonmonotonic functions of the light intensity. The data are interpreted as a result of an interaction between visual subsystems: the system which receives inputs from receptor cells R1-R6 is inhibited by the system of receptor cells R7 and R8, probably by R8 alone.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00605403
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  • 3
    Electronic Resource
    Electronic Resource
    Phase relationships in the system Ni-W-O and thermodynamic properties of NiWO4 (1977)
    Springer
    Journal of materials science 12 (1977), S. 1647-1652 
    Details
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The phase diagram of the Ni-W-O system at 1200 K was established by metallographic and X-ray identification of the phases present after equilibration at controlled oxygen potentials. The oxygen partial pressures over the samples were fixed by metered streams of CO+CO2 gas mixtures. There was only one ternary oxide, nickel tungstate (NiWO4), in the Ni-W-O system at a total pressure of 1 atm, and this compound decomposed to a mixture of Ni+WO2.72 on lowering the oxygen potential. The Gibbs' free energy of formation of NiWO4 was determined from the measurement of the e.m.f. of the solid oxide galvanic cell, Pt, Ni+NiWO4+WO2.72/CaO-ZrO2/Ni+NiO, Pt and thermodynamic properties of tungsten and nickel oxides available in the literature. For the reaction, NiO(s)+WO3(s)→NiWO4(s) ΔG°=−10500−0.708 T (±250) cal mol−1.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00542815
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  • 4
    Electronic Resource
    Electronic Resource
    Ion-exchange equilibria between (Mn, Co)O solid solution and (Mn, Co) Cr2O4 and (Mn, Co) Al2O4 spinel solid solutions at 1100° C (1977)
    Springer
    Journal of materials science 12 (1977), S. 481-488 
    Details
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The compositions of the (Mn,Co)O solid solution with rock salt structure in equilibrium with (Mn,Co)Cr2O4 and (Mn,Co)Al2O4 spinel solid solutions have been determined by X-ray diffraction measurements at 1100° C and an oxygen partial pressure of 10−10 atm. The ion exchange equilibria are quantitatively analysed, using values for activities in the (Mn,Co)O solid solution available in the literature, in order to obtain activities in the spinel solid solutions. The MnAl2O4-CoAl2O4 solid solution exhibits negative deviations from Raoult's law, consistent with the estimated cation disorder in the solid solution, while the MnCr2O4-CoCr2O4 solid solution shows slightly positive deviations. The difference in the Gibbs free energy of formation of the two pure chromites and aluminates derived from the results of this study are in good agreement with recent results obtained from solid oxide galvanic cells and gas-equilibrium techniques.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00540270
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  • 5
    Electronic Resource
    Electronic Resource
    Neue gas-chromatographische Methode zur quantitativen Bestimmung von 3α-Ätiocholanolon aus dem Plasma mit dem Alkaliflammendetektor (1976)
    Springer
    Fresenius' Zeitschrift für analytische Chemie 279 (1976), S. 158-159 
    Details
    ISSN: 1618-2650
    Keywords: Best. von 3α-Ätiocholanolon in Plasma ; Chromatographie, Gas ; Alkaliflammendetektor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00440825
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  • 6
    Electronic Resource
    Electronic Resource
    Massenspektrometrische Untersuchungen an Phosphinsäureestern von Monohydroxysteroiden (1976)
    Springer
    Fresenius' Zeitschrift für analytische Chemie 279 (1976), S. 163-164 
    Details
    ISSN: 1618-2650
    Keywords: Untersuchung von Monohydroxysteroiden ; Massenspektrometrie ; Phosphinsäureester
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00440830
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  • 7
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindungen von Übergangsmetallen. XX. [1]. Zur Reaktion von NiCl2 · 2PR3 und CoCl2 · 2PR3 mit LiSn(CH2C6H5)3 (1976)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 151-154 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XX. On the Reaction of NiCl2 · 2 PR3 and CoCl2 · 2 PR3 with LiSn(CH2C6H5)3LiSn(CH2C6H5)3 reacts with NiCl2 · 2 P(n-C4H9)3 in tetrahydrofuran forming benzyl nickel chloride, which could be isolated in form of the bipyridyl complex C6H5CH2-NiCl · dipy. NiCl2 · 2 P(C6H5)3 and CoCl2 · 2 P(C6H5)3 are reduced to complexes of the formula MCl · 2 P(C6H5)3 · 3 THF (M = Ni, Co).
    Notes: LiSn(CH2C6H5)3 reagiert mit NiCl2 · 2 P(n-C4H9)3 in Tetrahydrofuran zu Benzylnickelchlorid, das als Dipyridylkomplex isoliert werden konnte. Bei Einsatz von NiCl2 · 2 P(C6H5)3 und CoCl2 · 2 P(C6H5)3 erfolgt dagegen eine Reduktion zu Komplexen der Zusammensetzung MCl · 2 P(C6H5)3 · 3 THF (M = Ni, Co).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19764250209
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  • 8
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindugen von Übergangsmetallen. XXIX. Dibenzylmangan - Darstellung und Reaktionen (1979)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 455 (1979), S. 3-12 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXIX. Dibenzyl Manganese - Preparation and ReactionsManganese(II) acetylacetonate reacts with tribenzyl aluminium and dibenzyl magnesium forming the yellow complexes 3(C6H5CH2)2Mn · Al(acac)3 and (C6H5CH2)2Mn · Mg(acac)2 Dibenzyl manganese is also formed at the reaction of dibenzyl magnesium or benzyl magnesium chloride with MnCl2 · 1.5 THF and was separated as the dioxan complex (C6H5CH2)2Mn · 2C4H8O2, the ligands of which can be removed to a great extent in vacuum.Dibenzyl manganese reacts with CO2, CS2 and SO2 with insertion into the Mn-C-bonds. The corresponding manganese compounds were isolated and furtherly characterized.
    Notes: Mangan(II)-acetylacetonat reagiert mit Tribenzylaluminium bzw. Dibenzylmagnesium zu den gelben Komplexen 3(C6H5CH2)2Mn · Al(acac)3 bzw. (C6H5CH2)2Mn Mg(acac)2. Dibenzylmangan entsteht auch bei Einwirkung von Dibenzylmagnesium oder Benzyl magnesiumchlorid auf MnCl2 · 1,5 THF; eine Abtrennung von den Magnesiumsalzen gelingt in Form des 1,4-Dioxankomplexes (C6H5CH2)2Mn · 2C4H8O2, dessen Ligandenmoleküle im Vakuum weit gehend entfernt werden können.Dibenzylmangan reagiert mit CO2, CS2 und SO2 unter Insertion in die Mn-C-Bindungen. Die entsprechenden Mangansalze wurden isoliert und näher charakterisiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19794550101
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  • 9
    Electronic Resource
    Electronic Resource
    An experimental-numerical hybrid technique for three dimensional stress analysis (1977)
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 11 (1977), S. 1845-1863 
    Details
    ISSN: 0029-5981
    Keywords: Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: The paper describes a numerical method for determining the stress distribution in the interior of a three-dimensional body using experimentally determined surface stresses, and the interior displacements from surface displacements. The normal and shear stresses inside the body are obtained by solving Laplace's equation in terms of sum of normal stresses together with the three-dimensional compatibility equations in terms of stresses, using the finite difference technique, when the stresses on the surface of the body are known. On the other hand if surface displacements are known (from which strain components could be determined) then displacement components in the interior of a body can be determined by solving Laplace's equation in terms of sum of normal strains together with the three-dimensional equilibrium equations in terms of displacements. It is shown that axi-symmetric problems can also be solved in an identical way by transforming the equations into cylindrical co-ordinates. The application of the method has been illustrated through several examples.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/nme.1620111208
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  • 10
    Electronic Resource
    Electronic Resource
    Steroid phosphorus compounds. V - mass spectrometry of phosphinic esters of monohydroxy steroidsAbbreviations: E1 = estrone; A = androsterone; 3αEt = 3α-etiocholanolone; 3βEt = 3β-etiocholanolone; DHEA = dehydroepiandrosterone; DHT = 5α-dihydrotestosterone: T = testosterone: PO, PS and P = the dimethylphosphinic, dimethylthiophosphinic and dimethylphosphinous ester groups of the corresponding hydroxy steroid, respectively. (1976)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1976), S. 64-70 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of the dimethylphosphinic, dimethylthiophosphinic and dimethylphosphinous ester derivatives of several monohydroxy steroids are reported. The fragmentations of the derivatized steroids largely depend on the nature of the the phosphorus-containing ester group. Phenolic ester derivatives exhibit the base peak at the molecular ion, whereas the spectra of the secondary phosphinic esters are dominated by very intense protonated phosphinic acid ions [Me2 P(XH)(OH)]+ at m/e 95 (X = O) or at m/e 111 (X = S). The present results also indicate the low ionization potential for the phosphinic ester group. Due to their good gas chromatographic properties, these steroid derivatives appear to be particularly suitable for gas chromatographic mass spectrometric analysis of biochemical materials.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200030205
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