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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography B: Biomedical Sciences and Applications 414 (1987), S. 313-322 
    ISSN: 0378-4347
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography B: Biomedical Sciences and Applications 310 (1984), S. 188-192 
    ISSN: 0378-4347
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography B: Biomedical Sciences and Applications 309 (1984), S. 261-267 
    ISSN: 0378-4347
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Earth and Planetary Science Letters 62 (1983), S. 208-214 
    ISSN: 0012-821X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geosciences , Physics
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 8 (1975), S. 329-332 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Kyanite phases Al2SiO5 (I), Al2GeO5 (II) and Cr2GeO5 (III) were synthesized at 20 kb/1000°C (I, II) and at 1 atm/1150°C (III). Powder X-ray patterns for II and III are presented in comparison with that of I. Triclinic lattice constants are a0 = 7.127 (7.253, 7.422), b0 = 7.858 (8.011, 8.244), c0 = 5.570 (5.649, 5.815) Å, α = 89.99 (89.97, 90.58), β = 101.22 (101.23, 101.10), γ = 106.04 (106.05, 106.01)°, and V0 = 293.6 (308.9, 339.9) Å3 for the kyanite phases I (II, III, respectively). Infrared absorption spectra of I (II, III) were measured between 1400 and 200 cm−1. Band shifts produced by the isomorphous substitutions allow tentative band assignments of the Al2SiO5-kyanite spectrum: 1032, 1009, 940 cm−1 ν3 (SiO4); 898 cm−1 ν1 (SiO4); 720, 438 cm−1 ν4, ν2 (SiO4) ?; banes between 674 and 505 cm−1 and at 467 cm−1 are mainly due to octahedral Al–O vibrations.
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  • 6
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung Aus einer Granat (Gt)-Omphacit (Cpx)-Kyanit (Ky) Paragenese eines Eklogit Xenoliths aus dem Zagadochnaya Kimberlit, Jakutien (Grospydit Z13), wurden Einkristalle isoliert und mit polarisierter FTIR-Mikrospektrometrie im OH Valenzschwingungsbereich und mit der Elektronenstrahl-Mikrosonde untersucht. Die koexistierenden Minerale sind hinsichtlich ihrer Haupt- und Nebenelemente homogen und haben Zusammen setzungen von etwa Gross49Pyr26Alm20Uvar4 (Gt), Jad45Dio47Hed6Kos2 (Cpx) and Ky〉97 Einkristallspektren von Gt zeigen eine νOH-Bande bei 3630 cm−1) (Halbwerts breite ca. 100 cm−1) die wahrscheinlich von Schwingungen tetraedrischer (OH)4 4− Gruppen, die SiO4 4− Tetraeder ersetzen, herrührt. Cpx zeigt eine starke, aber schwach pleochroitische Bande bei 3464 cm−1 (Halbwertsbreite ca. 160 cm−1) and eine schwache, deutlich pleochroitische Satellitenbande bei 3620 cm−1) Ky OH Spektren zeigen zwei Gruppen von schwachen, scharfen pleochroitischen Banden, ein fur Hochdruck Ky charakteristisches Bandentriplett bei 3439, 3410, 3387 cm−1) and ein Bandendublett bei 3279, 3264 cm−1) (Halbwertsbreiten ca. 10 cm−1) Aus den integralen and linearen Extinktionen der nicht-polarisierten Spektren wurde der Defekt-Hydroxyl Gehalt der drei koexistierenden Minerale abgeleitet and mit O.OX Gew% H2O festgelegt. Das Verteilungsschema des Wasserstoffs kann in der Mineralparagenese mit cKy 〈 cCpx ≪ cGt angegeben werden.
    Notes: Summary Single crystals of paragenetic garnet (gt), omphacite (cpx) and kyanite (ky) were isolated from an eclogite xenolith from the Zagadochnaya kimberlite, Yakutia (grospydite Z13) and studied by polarized FTIR-microspectrometry in the OH valence vibrational region and by microprobe analyses. The coexisting minerals are homogeneous with respect to major and minor elements and have compositions near gross49pyr26alm20uvar4 (gt), jad45dio47hed6kos2 (cpx) and ky〉97. Single crystal spectra show one νOH-band for gt at 3630 cm−1 (halfwidth ca. 100 cm−1) which is very likely caused by vibrations of tetrahedral (OH)4-4− clusters replacing SiO4 4− tetrahedra. Cpx shows one strong, but weakly pleochroic band at 3464 cm−1 (halfwidth ca. 160 cm−1) and a weak satellite band centered at 3620 cm−1) with a distinct pleochroism. Ky OH spectra exhibit two sets of weak sharp pleochroic bands, a triplet, characteristic for high pressure ky, at 3439, 3410, 3387 cm−1) and a doublet at 3279, 3264 cm−1) (halfwidths ca. 10 cm−1) From integral and linear absorbances in the unpolarized spectra defect-hydroxyl contents in the three coexisting minerals were estimated and found near O.OX wt% H2O. The distribution scheme of hydrogen in the paragenetic minerals was evaluated to be cky 〈 ccpx ≪〈 cgt.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 56 (1976), S. 27-34 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Orthorhombic amphiboles with excess OH, which can be schematically deduced from anthophyllite by the combined substitutions Mg2+ + O2−→Li++OH− and Mg2+→2 Li+, were synthesized at 750–875° C/1 kbar $$P_{{\text{H}}_{\text{2}} {\text{O}}}$$ in the system Li2O-MgO-SiO2-H2O. Their phase relations are presented for 800° C/1 kbar $$P_{{\text{H}}_{\text{2}} {\text{O}}}$$ . An amphibole with the analytical composition 2.70 wt% Li2O, 31.1 wt% MgO, 63.0 wt% SiO2, and 3.29 wt% H2O has lattice constants a 0 18.588 (11), b 0 17.966 (10), c 0 5.262 (3) Å, V 0 1,757.2 (1.5) Å3 (referred to Space Group Pnma). The OH-valence vibrational spectrum of this amphibole showed v OH bands at 3,667, 3,708, and 3,725 (shoulder) cm−1, which are ascribed to OH in the configurations (MgMgMg)-OH, (MgMgMg)-OH-Li (Li in the A-site) of the pseudotrigonal (M1M1M3)-OH arrangement in the amphibole structure, and to Si-OH, respectively. No explanation can at present be offered for an additional shoulder at 3,695 cm−1. The proposed structural formula is (Li0.27 □0.73)(Li1.11 Mg0.89)· (Mg5)(Si8.01O21.20(OH)0.80)(OH)2.00.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 7 (1974), S. 659-662 
    ISSN: 1612-1112
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung 6 polare und 8 unpolare PTH-Aminosäuren wurden an einem “reversed phase”-System aus Corasil C18 und zwei Wasser/Acetonitril/Isopropanol-Gemischen, die sich lediglich im Wassergehalt unterscheiden, flüssig-chromatographisch getrennt. Bei Anwendung eines Stufengradienten aus beiden Elutionsmischphasen gelang die Trennung der 14 PTH-Derivate in einem Durchlauf in weniger als 40 Minuten. Die Vorteile des angewandten Systems liegen in der guten Reproduzierbarkeit der Retentionswerte, die eine sichere Identifizierung der einzelnen PTH-Aminosäuren zuläßt.
    Notes: Summary 6 polar and 8 nonpolar PTH-amino acids have been separated using a “reversed phase” liquid chromatographic system with Corasil C18 and two water/acetonitrile/isopropanol mixtures, differing only in the water content, as mobile phases. Employing a stepped gradient of these two mobile phases, the elution of 14 PTH derivatives was accomplished in one run in less than 40 minutes. This system has the advantage of giving retention parameters of high reproducibility for the unambiguous identification of the different PTH-amino acid derivatives.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 28 (1970), S. 9-18 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The pseudobinary section Al2SiO5-“Cr2SiO5” of the system Al2O3-Cr2O3-SiO2 has been investigated at 20 and 30 kb pressure in the temperature range 1,000–1,600° C. The solubility of “Cr2SiO5” in kyanite (Al2SiO5) extends up to 24 mole % “Cr2SiO5” at 20 kb and 31 mole % at 30 kb. The extent of this solid solution is not notably dependent on temperature in the range studied. The stability of kyanite is increased by the substitution Cr ⇌ Al by about 80° C at 20 kb as compared to Cr-free kyanite. Cr-poor sillimanite and Cr-rich kyanite can stably coexist in a temperature interval of up to 80° C at 20 kb and about 150° C at 25 kb.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 41 (1973), S. 31-46 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Iron- and vanadium-bearing kyanites have been synthesized at 900 and 1100° C/20 kb in a piston-cylinder apparatus using Mn2O3/Mn3O4- and MnO/Mn-mixtures, respectively, as oxygen buffers. Solid solubility on the pseudobinary section Al2SiO5-“Fe2SiO5”(-“V2SiO5”) of the system Al2O3-Fe2O3(V2O3)-SiO2 extends up to 6.5 mole% (14mole %) of the theoretical end member “FeSiO5”(“V2SiO5”) at 900°C/20 kb. For bulk compositions with higher “Fe2SiO5” (“V2SiO5”) contents the corundum type phases M2O3(M = Fe3+, V3+) are found to coexist with the Fe3+(V3+)-saturated kyanite solid solution plus quartz. The extent of solid solubility on the join Al2SiO5-“Fe2SiO5” at 1 100°C was not found to be significantly higher than at 900° C. Microprobe analyses of iron bearing kyanites gave no significant indication of ternary solid solubility in these mixed crystals. Lattice constants a 0, b 0, c 0, and V0 of the kyanite solid solutions increase with increasing “Fe2SiO5”- and “V2SiO5”-contents proportionally to the ionic radii of Fe3+ and V3+, respectively, the triclinic angles α,β,γ remain constant. Iron kyanites are light yellowish-green, vanadium kyanites are light green. Iron kyanites, (Al1.87 Fe 0.13 3+ )SiO5, were obtained as crystals up to 700 μm in length.
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