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  • Chemistry  (8)
  • Engineering General  (1)
  • Massenspektrometrie  (1)
  • thermochemical diagrams  (1)
  • 1975-1979  (11)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 13 (1979), S. 25-55 
    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.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 11 (1977), S. 1845-1863 
    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.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 279 (1976), S. 163-164 
    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
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  • 4
    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.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1978), S. 302-311 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of 20 differently substituted dimethylthiophosphinic esters of aromatic hydroxy compounds are presented. Fragmentation routes were investigated using high resolution mass measurements, decoupled metastable determinations and deuterium labelling. All compounds exhibited abundant molecular ions and typical phosphorus-containing ions. Characteristic elimination processes strongly dependent upon the respective type of substitution were observed. Due to their high stability, their great ease of formation and their good gas chromatographic properties these new types of derivatives are of special interest for establishing gas chromatography mass spectrometry profiles of acidic catecholamine metabolites.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 151-154 
    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.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 447 (1978), S. 136-142 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contribution to the Chemistry of Transition Metal Alkyl Compounds. XXVIII. Benzylation of the Trivalent Titanium, Vanadium, and Chromium AcetylacetonatesBzCr(acac)2, 2Bz(Vacac)2 · Mg(acac)2 and 3BzV(acac)2 · Al(acac)3 were obtained in definite form by reaction of Cr(acac)3 and V(acac)3 with Bz3Al, Bz2Mg, and BzMgCl. Ti(acac)3, reacts with Bz2Mg and BzLi forming deep green Bz3Ti, which could'nt be isolated free of impurities (Bz = C6H5CH2, acacH = acetylacetone).
    Notes: Bei Reaktionen von Cr (acac)3 und V(acac)3 mit Bz3Al, Bz2Mg und BzMgCl wurden als definierte Verbindungen BzCr(acac)2, 2BzV(acac)2 · Mg(acac)2 und 3BzV(acac)2, Al(acac)3 erhalten. Aus Ti(acac)3 und Bz2Mg bzw. BzLi entsteht tiefgrünes Bz3Ti, das jedoch nicht frei von Verunreinigungen erhalten werden konnte. (Bz = C6H5CH2, acacH = Acetylaceton).
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 455 (1979), S. 3-12 
    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.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 415 (1975), S. 109-114 
    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. XVI. On the Existence and Synthesis of Benzyl Nickel CompoundsIt is reported on experiments for benzylating nickel chloride and its triaryl and trialkylphosphine complexes by means of benzyl magnesium halides. Attempts for preparation of simple “binary” nickel benzyls failed, but it was possible to synthesize some o-substituted benzyl nickel compounds stabilized by trialkyl phosphines of the type
    Notes: Es wird über Versuche zur Benzylierung von Nickelchlorid und dessen Triaryl- und Trialkylphosphinkomplexen mittels Benzylmagnesiumhalogeniden berichtet. Während Versuche zur Gewinnung einfacher „binärer“ Nickelbenzyle fehlschlugen, gelang die Synthese einiger trialkylphosphinstabilisierter Benzylnickelderivate mit o-ständigen Substituenten in den Benzolringen vom Typ
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 421 (1976), S. 129-134 
    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. XVIII. On the Preparation and Properties of Tetrabenzyl Vanadium and Benzyl Tantalum ChloridesPure tetrabenzyl vanadium was isolated and characterized by elementary analyses, EPR and 1H-NMR spectra, by hydrolysis and thermal decomposition.  -  Experiments for the preparation of tetra or pentabenzyl compounds of niobium and tantalum failed, but we could prepare C6H5CH2TaCl4, (C6H5CH2)2TaCl3, and (C6H5CH2)3TaCl2, the last two in form of bipyridyl complexes.
    Notes: Vanadintetrabenzyl wurde in definierter Form isoliert und durch Elementaranalyse, ESR- und 1H-NMR-Spektrum sowie durch die hydrolytische und thermische Spaltung charakterisiert.  -  Versuche zur Gewinnung von Tetra- und Pentabenzylverbindungen des Niobs und Tantals blieben erfolglos. Es gelang jedoch, die Verbindungen C6H5CH2—TaCl4, (C6H5CH2)2TaCl3 und (C6H5CH2)3TaCl2, zum Teil in Form von Dipyridylkomplexen, zu gewinnen.
    Additional Material: 2 Ill.
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