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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Numerische Mathematik 4 (1962), S. 330-335 
    ISSN: 0945-3245
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Numerische Mathematik 3 (1961), S. 169-173 
    ISSN: 0945-3245
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Genomics 19 (1994), S. 75-85 
    ISSN: 0888-7543
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography A 193 (1980), S. 476-479 
    ISSN: 0021-9673
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Fluorine Chemistry 3 (1973), S. 167-178 
    ISSN: 0022-1139
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Mineralogy and petrology 47 (1992), S. 87-101 
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung Ce- und La-Bastnäsite, sowie deren OH-Analoga wurden synthetisiert und ihre Stabilitätsbeziehunger beiP f = 1 kbar undT = 400 bis 900°C wurden im System (Ce,La)F-H-C-O bestimmt. Die anfänglichen Flüssigkeitszusammensetzungen waren so, daß $$P_{CO2} \approx \frac{1}{2}P_f $$ und die HF/(HF + H2O)-Verhältnisse 0–0.172 waren. Röntgenpulver- und Ultrarot-Untersuchungen zeigten, daß Bastnäsite, die mit anfänglich HF-armen Flüssigkeiten equilibriert wurden, alle an F angereichert sind. Hydroxilbastndsit-(La) ist bis 810°C und Fluorbastnäsit-(La) bis 860°C stabil. Ihre festen Zersetzungsprodukte sind La2O2O3, bzw. LaOF. Die Stabilität der Ce-Bastnäsite hängt etwas von $$f_{0_2 } $$ ab. Hydroxilbastnäsit-(Ce) ist bei $$f_{0_2 } $$ des Eisen-Quarz-Fayalit-Puffers bis 660°C stabil und mit Magnetit-Hämatit-Puffer bis 640°C. Das feste Zerfallsprodukt ist für das Hydroxil-Glied nur CeO2, für das Fluor-Glied eine Mischung aus CeO2, CeF3 und CeOF. Faktoren, welche die Stabilität der einzelnen Spezies beeinflussen, werden diskutiert, wie das Verhältnis OH zu F, $$f_{0_2 } $$ und die Gesamtzusammensetzung. Petrogenetische Folgerungen aus der vorliegenden Studie schließen ein, daß Bastnäsite von hydrothermalen bis zu magmatischen Bedingungen stabil sein können, daß sich an F angereicherte Glieder in relativ F-armer Umgebung bilden können, und daß OH-Glieder selten sind und nur unter Bildungsbedingungen niedriger Temperatur und weitgehender Abwesenheit von F auftreten.
    Notes: Summary Bastnaesites of Ce and La and their OH-analogs were synthesized and their stability relations were determined atPf = 1 kbar andT = 400 to 900°C in a part of the system (Ce,La)-F-H-C-0. The initial fluid compositions were such that $$P_{CO_2 } \approx \frac{1}{2}P_f $$ and HF/(HF + H2O) ratios were 0 to 0.172. XRD and IR studies indicate that bastnaesites equilibrated in initial fluids low in HF are all F-enriched. The hydroxylbastnaesite-(La) is stable up to 810°C and the fluorbastnaesite-(La) is stable up to 860°C. Their condensed breakdown products are La2O2CO3 and LaOF, respectively. The stability of Ce bastnaesites is slightly $$f_{0_2 } $$ dependent. The hydroxylbastnaesite-(Ce) is stable up to 660°C at the $$f_{0_2 } $$ defined by the IQF buffer and up to 640°C by the MH buffer. The fluorbastnaesite-(Ce) is stable up to 800°C at the $$f_{0_2 } $$ defined by the IQF and up to 760°C by the MH buffer. The condensed breakdown product for the hydroxyl end-member is simply CeO2 but for the fluorine one is a combination of CeO2, CeF3, and CeOF. Factors, such as OH vs F, $$f_{0_2 } $$ , and bulk composition, that affect the stability of individual species are discussed. Petrogenic implications resulting from the present study include that bastnaesites can be stable from hydrothermal to magmatic conditions, that F-enriched species can form in an environment relatively low in F content, and that OH-species are rare and occur only in low-temperature environments essentially devoid of F.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 112 (1992), S. 385-392 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The stability of merwinite (Mw) and its equivalent assemblages, akermanite (Ak)+calcite (Cc), diopside (Di)+calcite, and wollastonite (Wo)+monticellite (Mc)+calcite was determined at T=500–900° C and P f=0.5–2.0 kbar under H2O−CO2 fluid conditions with X CO 2=0.5, 0.1, 0.05, and 0.02. Merwinite is stable at P f=0.5 kbar with T〉700° C and X CO 2〈0.1. At P f=2.0 kbar, the assemblage Di+Cc replaces merwinite at all T and X CO 2 conditions. At intermediate P f=1 kbar, the assemblage Ak+Cc is stable above 707° C and Wo+Mc+Cc is stable below 707° C. The univariant curve for the reaction Di+Cc=Wo+Mc+CO2 is almost parallel to the T axis and shifts to low P f with increasing X CO 2, with the assemblage Di+Cc on the high-P f side. The implications of the experimental results in regard to contact metamorphism of limestone are discussed using the aureole at Crestmore, California as an example.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 71 (1980), S. 407-415 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The phase relations in the system grossular-spessartine-H2O were investigated at 2.0 Kb aqueous fluid pressure and at subsolidus temperatures down to 420 ° C. Despite metastable persistence of a compositional gap found in some intermediate members, a complete solid solution between grossular and spessartine exists. Linear relations between the unit cell edge, a 0, and composition were readily observed down to 620 ° C with a 0=11.849(2) Å and 11.613(2) Å for grossular and spessartine, respectively. Hydrated garnets began to appear at higher temperature for the Ca-rich members. Grossular and spessartine formed at 420 ° C have a 0=11.901(2) Å and 11.632(2) Å, indicating the presence of 0.6 and 0.2 mol H2O, respectively. Intermediate members show varying degrees of hydration. Infrared spectra of the more hydrated members show a major and minor absorption bands at 3,620 cm−1 and 3,660 cm−1, respectively, in addition to a broad band around 3,430 cm−1. All the hydrogarnets formed at 420 ° C were proven to be metastable. The rare occurrence of the intermediate grossular-spessartine garnets may be attributed to the lack of appropriate bulk chemistry of the rock rather than to the P-T conditions to which the rock is subjected. There may be a stability field for hydrogrossular below 420 ° C at 2 Kb, but not for hydrospessartine. Any occurrence of hydrogarnet may be used as a temperature indicator setting the maximum of formation for the hydrogarnet-bearing assemblage below 420 ° C at 2 Kb.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 118 (1994), S. 314-320 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The rare mineral cymrite, BaAl2Si2O8·H2O, was discovered in Nevada in a Cambrian bedded barite sequence that exhibits low-grade metamorphism. The mineral occurs exclusively in thin-bedded siliceous rock containing anhedral pyrite crystals up to 1 cm. Cymrite forms rectangular grains ca 40 μm across, distributed throughout the chalcedonic quartz matrix. An SEM image of one such blocky grain shows that it is filled by tiny aggregates, instead of a single crystal of cymrite. This cymrite may have replaced a pre-existing rectangular mineral, most likely barite. The Nevada occurrence of cymrite prompted a restudy of its stability relations. Conventional hydrothermal techniques were adopted in the experimental work with run durations up to 7 months. The univariant curve for the dehydration reaction: BaA12Si2O8· H2O -BaA12Si2O8 +H2O passes the following reversed brackets: 300–315° C at 3 kbar, 290–300° C at a 2 kbar, 270–285° C at 1 kbar, and 240–270° C at 0.5 kbar. These results indicate that cymrite can be stable at much lower pressures than those previously reported. The replacement of barite by cymrite was experimentally demonstrated with an alkaline solution as depicted by the reaction: BaSO4+2OH-+A12O3-2SiO2=BaA12Si2O8·H2O+SO 4 2 Such replacement failed to take place when an acidic solution was used instead.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    BIT 30 (1990), S. 114-125 
    ISSN: 1572-9125
    Keywords: Oscillatory integral ; Asymptotic expansion ; Compound precision ; Gauss-Laguerre quadrature ; Markov numerical differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract A constructive process is presented which leads to a class of quadrature formulas with any preassigned compound precision for the numerical integration of rapidly oscillating functions on (0, ∞) of the forme −x F(x, λx), whereλ is a large parameter andF(·,y) is periodic of period unity iny. 1980 Mathematics Subject Classification, Primary 41A55, Scondary 41A60
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