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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Mineralium deposita 1 (1967), S. 278-306 
    ISSN: 1432-1866
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung Die Phasenbeziehungen in den Systemen Ag-Bi-S, Bi-Pb-S und Ag-Pb-S wurden durch Versuche in evakuierten Quarzglasröhrchen bestimmt. Die Auswertung aller experimentellen Daten gestattete eine Extrapolation der Phasenbeziehungen im quaternären System Ag-Bi-Pb-S. — Im System Ag-Bi-S besteht ein Zwei-Schemlzenfeld im metallreichen Teil über 597±3°C und im schwefelreichen Teil über 563±3°C. Die ternären Phasen entsprechen den Mineralien Schapbachit (AgBiS2) und Pavonit (AgBi3S5). Zwischen 802±2°C und 343±2°C ist die Paragenese Silberglanz (Ag2S) + Bi-reiche Schmelze stabil; unterhalb 343°C wird sie jedoch ersetzt durch die Paragenese Silber + Schapbachit. — Fünf ternäre Phasen sind stabil im Schnitt PbS-Bi2S3 oberhalb von 400°C: Phase II (18 Mol-% Bi2S3), Phase III (27 Mol-% Bi2S3), „Cosalite“ (33.3 Mol-% Bi2S3), Phase IV (51 Mol-% Bi2S3) und Phase V (65 Mol-% Bi2S3). Phase IV entspricht dem Mineral Galenobismutit und ist stabil unterhalb 750±3°C. Die Phasen II, III und V kommen zwar nicht in der Natur vor, jedoch weisen typische myrmekitische und lamellare Gefüge, die man häufig in Pb-Bi-Sulfosalzen und deren Verwachsungen mit Bleiglanz beobachtet, auf die ehemalige Existenz solcher Phasen in diesen Erzen hin. Die Phasen II und III sind stabil von 829±6°C bzw. 816±6°C bis unter 200°C. Die Phase V, die im reinen System Bi-Pb-S zwischen 730±5°C und 680±5°C auftritt, wird in Gegenwart von 2% Ag2S stabilisiert bis herab zu 625±5°C. Versuche mit natürlichen Cosaliten lassen darauf schließen, daß diese Phase nur unterhalb 425±25°C in Gegenwart einer Gasphase stabil ist. — Im System Ag-Pb-S ist die Paragenese Silber-Bleiglanz unterhalb von 784±2°C stabil, die Paragenese Silberglanz-Bleiglanz dagegen unterhalb 605±5°C. — Die Mischkristallreihe von Schapbachit und Bleiglanz ist vollständig oberhalb 215±15°C; unterhalb dieser Temperatur entstehen charakteristische Entmischungsgefüge ähnlich den Widmannstättenschen Figuren. Für das quaternäre System werden schematische Phasenbeziehungen für 1050°C, 400°C und eine noch tiefere Temperatur gegeben.
    Notes: Abstract Phase relations within the Ag-Bi-S, Bi-Pb-S, and Ag-Pb-S systems have been determined in evacuated silica tube experiments. Integration of experimental data from these systems has permitted examination and extrapolation of phase relations within the Ag-Bi-Pb-S quaternary system. — In the Ag-Bi-S system liquid immiscibility fields exist in the metal-rich portion above 597±3°C and in the sulfur-rich portion above 563±3°C. Ternary phases present correspond to matildite (AgBiS2) and pavonite (AgBi3S5). Throughout the temperature range 802±2°C to 343±2°C the assemblage argentite (Ag2S) + bismuth-rich liquid is stable; below 343°C this assemblage is replaced by the assemblage silver + matildite. — Five ternary phases are stable on the PbS-Bi2S3 join above 400°C — phase II (18 mol-% Bi2S3), phase III (27 mol-% Bi2S3), “cosalite” (33.3 mol-% Bi2S3), phase IV (51 mol-% Bi2S3), and phase V (65 mol-% Bi2S3). Phase IV corresponds to the mineral galenobismutite and is stable below 750±3°C. Phases II, III, and V do not occur as minerals, but typical lamellar and myrmekitic textures commonly observed among the Pb-Bi sulfosalts and galena evidence their previous existence in ores. Phase II and III are stable from 829±6°C and 816±6°C, respectively, to below 200°C; Phase V, stable only between 730±5°C and 680±5°C in the pure Bi-Pb-S system is stabilized to 625±5°C by the presence of 2% Ag2S. Experiments conducted with natural cosalites suggest that this phase is stable only below 425±25°C in the presence of vapor. — In the Ag-Pb-S system the silver-galena assemblage is stable below 784±2°C, whereas the argentite + galena mineral pair is stable below 605±5°C. — Solid solution between matildite and galena is complete above 215±15°C; below this temperature characteristic Widmanstätten structure-like textures are formed through exsolution. Schematic phase relations within the quaternary system are presented at 1050°C, at 400°C, and at low temperature.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing, Ltd.
    The @international journal of nautical archaeology 34 (2005), S. 0 
    ISSN: 1095-9270
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Archaeology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 4 (1979), S. 317-339 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Systematic trends in the geometry of 149 oxide and 80 sulfide binary and ternary spinels have been examined from the standpoint of ionic radius and electronegativity. The mean ionic radii of the octahedral and tetrahedral cations, taken together, account for 96.9 and 90.5% of the variation in the unit cell parameter, a, of the oxides and sulfides, respectively, with the octahedral cation exerting by far the dominant influence in sulfides. The mean electronegativity of the octahedral cation exerts an additional, but small, influence on the cell edge of the sulfides. The equation a=(8/3√d)d tet+(8/3)d oct, where d tet and d oct are the tetrahedral and octahedral bond lengths obained from the sum of the ionic radii, accounts for 96.7 and 83.2% of the variation in a in the oxides and sulfides, respectively, again testifying to the applicability of the hard-sphere ionic model in the case of the spinel structure. Comparison of observed and calculated u values for 94 spinels indicates that up to 40% of the experimentally measured anion coordinates may be significantly in error. In addition to these compounds, u values are given for 52 spinels for which no data have previously been determined. Diagrams are presented for the rapid interpretation of the internal consistency of published data and the prediction of the structural parameters of hypothetical or partially studied spinels.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-9915
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Ethnic Sciences
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Research in higher education 5 (1976), S. 83-94 
    ISSN: 1573-188X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Nature of Science, Research, Systems of Higher Education, Museum Science
    Notes: Abstract The object of this paper is to analyze some of the factors underlying differing levels of morale in university departments. Morale is conceived to be primarily a product of perceived department-head performance, although it is also suggested that environmental and satisfaction variables may be important. Morale is seen as a potential symptomatic attribute which might be used in diagnosing organizational difficulties. The authors did indeed find, using multiple discriminant analysis on departmentally aggregated data, that the perceived performance of department heads was more important in predicting levels of morale. In addition, department size was also found to be useful. The conclusions drawn were that morale could be used as a symptom of departmental (or organizational) well being and that such data could be useful to those managing department heads both in the selection of department heads and in their ongoing supervision.
    Type of Medium: Electronic Resource
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