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  • 1995-1999  (26)
  • 1980-1984  (43)
  • 1960-1964  (7)
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  • 1
    Digitale Medien
    Digitale Medien
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Maschinenbau , Physik
    Notizen: A composition-graded solid electrolyte has been used to determine the standard Gibbs free energy of formation of lanthanum zirconate (La2Zr2O7) from the component oxides lanthana (La2O3) (A-rare earth) and zirconia (ZrO2) (monoclinic) in the temperature range of 870–1240 K. The cell used for measurement can be represented as Pt, O2, CaO + CaF2∥ CaF2| (LaF3)x(CaF2)1-x∥LaF3+ La2Zr2O7+ ZrO2, O2, Pt x=0 x=0.32 A composition-graded electrolyte has been introduced to compensate the solubility effects of the electrode material (lanthanum fluoride, LaF3) in the solid electrolyte (calcium fluoride, CaF2). The ability of the graded electrolyte to gen-erate a Nernstian response is demonstrated, using electrodes with known fluorine chemical potentials. For the reaction La2O3 (A-rare earth) + 2ZrO2 (monoclinic) → La2Zr2O7 (pyrochlore), the Gibbs free energy change (ΔG°f,ox) is given by the formula −133800 −10.32T (±4500) (in units of J/mol). The enthalpy and entropy of formation of La2Zr2O7 obtained in this study are in good agreement with calorimetric data. The “third-law” enthalpy of formation of La2Zr2O7, from the component oxides at 298.15 K, is −133.8 ± 5 kJ/mol.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Maschinenbau , Physik
    Notizen: Solid-state miscibility gap in the pseudo-binary calcium oxide-strontium oxide (CaO-SrO) system is delineated by X-ray diffractometry studies on samples equilibrated either under vacuum or in a flowing inert-gas atmosphere at temperatures of 973-1273 K. For the CaxSr1−xO solid solution, an asymmetric phase boundary that is characterized by a critical temperature of 1173 (±3) K and a composition of x= 0.53 (±0.01) is obtained. The excess Gibbs energy of mixing of the solid solution, which is derived from the experimental phase-boundary compositions and temperatures, can be represented by the expression ΔGE=x (1−x)[(27040 − 5.82 T) x+ (24915 − 5.34 T)(1 −x)] (in units of J/mol). It is necessary to include excess entropy terms to obtain a good fit to the experimental data. The chemical spinodal curve is computed from the thermodynamic parameters. The results obtained in this study are compared with phase-diagram and calorimetric information that is available in the literature.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Maschinenbau , Physik
    Notizen: The standard Gibbs energy of formation of the spinel MgAl2O4 from component oxides, MgO and α-Al2O3, has been determined in the temperature range 900 to 1250 K using a solid-state cell incorporating single-crystal CaF2 as the solid electrolyte. The cell can be represented as—Pt,O2,MgO+MgF2|CaF2|MgF2+MgAl2O4+α-Al2O3,O2,Pt—The standard Gibbs energy of formation from binary oxides, computed from the reversible emf, can be represented by the expression—capdeltaG°f,ox=−23600 − 5.91T(±150) J/mol—The ‘second-law’ enthalpy of formation of MgAl2O4 obtained in this study is in good agreement with high-temperature solution calorimetric studies reported in the literature.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 192 (1961), S. 288-289 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] From a selection of X-ray-irradiated progenies of 70,000 r. treatment of the X, generation of Gor-ohorua olitorius (i7.nO 632) in 1960, seven variants were found from a culture of healthy, vigorously growing normal plants. These plants with comparatively slender stom and small leaves were very ...
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Journal of applied electrochemistry 13 (1983), S. 55-67 
    ISSN: 1572-8838
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Elektrotechnik, Elektronik, Nachrichtentechnik
    Notizen: Abstract The open circuit potentials of the galvanic cell,Pt (or Au)¦(Ar + H2S + H2)′∥CaS + ZrO2(CaO)∥ (Ar + H2S+ H2)″£t (or Au) has been measured in the temperature range 1000 to 1660 K and PH2S:PH 2 ratios from 1.73×10−5 to 2.65×10−1. The solid electrolyte consists of a dispersion of calcium sulphide in a matrix of calcia-stabilized zirconia. The surface of the electrolyte is coated with a thin layer of calcium sulphide to prevent the formation of water vapour by reaction of hydrogen sulphide with calcium oxide or zirconia present in the electrolyte. The use of a ‘point electrode’ with a catalytically active tip was necessary to obtain steady emfs. At low temperatures and high sulphur potentials the emfs agreed with the Nernst equation. Deviations were observed at high temperatures and low sulphur potentials, probably due to the onset of significant electronic conduction in the oxide matrix of the electrolyte. The values of oxygen and sulphur potentials at which the electronic conductivity is equal to ionic conductivity in the two-phase electrolyte have been evaluated from the emf response of the cell. The sulphide-oxide electrolyte is unsuitable for sulphur potential measurements in atmospheres with high oxygen potentials, where oxidation of calcium sulphide may be expected.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Journal of applied electrochemistry 13 (1983), S. 469-472 
    ISSN: 1572-8838
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Elektrotechnik, Elektronik, Nachrichtentechnik
    Notizen: Abstract Single phase sodiumβ-alumina solid electrolyte was found to undergo isothermal phase separation in electrochemical cells, where a large oxygen potential gradient was imposed across the electrolyte and electrodes, not reversible to sodium ions, were short circuited. The experimental conditions and evidence of decomposition are outlined and a thermodynamic explanation for the phenomenon is given. This finding may lead to new methods for making multi-layered ceramic materials involving ionic conductors.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Monatshefte für Chemie 128 (1997), S. 337-351 
    ISSN: 1434-4475
    Schlagwort(e): Vanadium ; Thallium ; Heterobimetallic ; 2-(Dimethylaminomethyl)ferrocenyl ; Orthometallation ; Electron transfer ; Möβbauer spectroscopy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Summary Syntheses and properties of 2-(dimethylaminomethyl)ferrocenylderivatives of the composition (FcN) n VCl3−n (FcN=2-(dimethylaminomethyl)ferrocenyl;n=1 (1), 2 (2), 3 (3)), which are formed from VCl3·3THF and (FcN) Li (I), are reported. WhereasCp 2VCl2 (Cp=C5H5) reacts withI under formation ofCp 2V(FcN) (4), VO(acac)2 (acac=anion of acetylacetonate, C5H7O2) can be transformed into the 2-(dimethylaminomethyl)-ferrocenyl compound of tetravalent vanadium (FcN)VO(acac),5). However, when VOCl2·2THF reacts withI, the organovanadium(III)-derivative Li[(FcN)2V(O)Cl] (6) is formed. Reactions of VCl4·2THF,Cp 2VCl2, VOCl3, andCpVOCl2 with (FcN)3Tl (II) lead to thermally instable vanadiumorganic compounds under formation of (FcN)2TlCl (7). A detailed characterization of1–7 was carried out by elementary analysis, determination of effective magnetic moments, IR, mass and1H NMR spectroscopy as well as — especially referring to the formation of possible chelate structures — by UV/Vis andMöβbauer spectroscopy.
    Notizen: Zusammenfassung Synthesen und Eigenschaften von 2-(Dimethylaminomethyl)ferrocenyl-Derivaten der Formel (FcN) n VCl3−n (FcN=2-(Dimethylaminomethyl)ferrocenyl;n=1 (1), 2 (2), 3 (3)), die aus VCl3·3THF und (FcN) Li (I) entstehen, werden mitgeteilt. WährendCp 2VCl2 (Cp=C5H5) mitI unter Bildung vonCp 2 V(FcN) (4) reagiert, läßt sich VO (acac)2 (acac=Anion des Acetylacetonates, C5H7O2) in die 2-(Dimethylaminomethyl)ferrocenyl-Verbindung des vierwertigen Vanadiums (FcN)VO(acac),5) überführen. Dagegen entsteht bei Umsetzungen von VOCl2·2THF mitI das Organovanadium (III)-Derivat Li [(FcN)2V(O)Cl] (6). Reaktionen von VCl4·2THF,Cp 2VCl2, VOCl3 undCpVOCl2 mit (FcN)3Tl (II) führen unter Bildung von (FcN)2TlCl (7) zu thermisch instabilen vanadiumorganischen Verbindungen. Eine eingehende Charakterisierung von1–7 erfolgte durch Elementaranalysen, Ermittlung der effektiven magnetischen Momente, IR-, Massen- und NMR-Spektroskopie sowie, insbesondere hinsichtlich der Ausbildung möglicher Chelatstrukturen, durch UV/Vis und Mößbauer-Spektroskopie.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    ISSN: 1434-4475
    Schlagwort(e): Organolanthanides ; Heterobimetallic complexes ; Ferrocene ; Mößbauer spectroscopy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary Reactions of 2-(dimethylaminomethyl)ferrocenyl-lithium ((FcN)Li,1) with various cerium(IV) precursors lead to the formation of heterobimetallic organocerium(III) complexes. The compounds Li3[(FcN)2CeF4(THF)3] (2), (FcN)2CeF(DME)2 (3), Li4[(FcN)CeCl6] (4), and Li[(FcN)CeCl3(DME)] (5) have been isolated by redox reactions. Similar treatment of (C5Me5)2 Ce(μ-Cl)2K(THF)2 with one equivalent of1 affords the neutral species (C5Me5)Ce(FcN)Cl (6)via displacement of one C5Me5 ligand. Complexes of the type (C5Me5)Ln(FcN)Cl have also been isolated forLn=Pr (7), Nd (8), and Sm (9). These and related heterobimetallic lanthanideFcN complexes have been studied by Mößbauer spectroscopy.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    Archive of applied mechanics 32 (1963), S. 51-65 
    ISSN: 1432-0681
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    International journal of earth sciences 85 (1996), S. 29-37 
    ISSN: 1437-3262
    Schlagwort(e): Banded mineralization ; Harz mountains ; Self-organization ; Iron, manganese, ferrihydrite, birnessite ; Time-series analysis ; Aquatic systems ; Iron bacteria ; Ostwald ripening
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie
    Notizen: Abstract A recent early diagenetic banded iron-manganese mud has been forming underground in a closed lead-zinc mine for approximately 40 years. The processes leading to the banded structure of the precipitate were studied during a period of 2 years. Therefore, 19 physical and chemical parameters were measured regularly in short intervals. The resulting time series were analysed with respect to the data sets of the monthly chemical analyses of the descendent mine water, the daily rainfall and the mineral content. The results reveal that the precipitated material undergoes internal self-organization due to interaction of redox, colloid-chemical, microbial, electrical and ripening processes, and not exclusively produced by seasonal fluctuations of material input. Thus, the primary banding of the material, caused by externally forced fluctuations of the redox conditions within the mine water, is reorganized after a short time. The finally observed bands are controlled by non-linear coupling of reaction and transport processes within the mud. A genetic model for the banded mineralization was developed and verified by numerical simulation.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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