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  • 1
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    In:  Nature, Luxembourg, Inst. Electrical & Electronics Engineers, vol. 395, no. 6697, pp. 62-65, pp. B06303, (ISSN: 1340-4202)
    Publication Date: 1998
    Keywords: Seismology ; hot ; spot ; Plate tectonics ; Surface waves ; Tomography ; Dispersion
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  • 2
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    In:  Earth planet. Sci. Lett., Luxembourg, Inst. Electrical & Electronics Engineers, vol. 197, no. 3-4, pp. 261-272, pp. B06303, (ISSN: 1340-4202)
    Publication Date: 2002
    Keywords: GeodesyY ; ConvolutionE ; hot ; spot ; Seismology ; EPSL
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  • 3
    Publication Date: 2016-12-21
    Description: We revisit the problem of coseismic rupture of the 2008 M w 7.9 Wenchuan earthquake. Precise determination of the fault structure and slip distribution provides critical information about the mechanical behaviour of the fault system and earthquake rupture. We use all the geodetic data available, craft a more realistic Earth structure and fault model compared to previous studies, and employ a nonlinear inversion scheme to optimally solve for the fault geometry and slip distribution. Compared to a homogeneous elastic half-space model and laterally uniform layered models, adopting separate layered elastic structure models on both sides of the Beichuan fault significantly improved data fitting. Our results reveal that: (1) The Beichuan fault is listric in shape, with near surface fault dip angles increasing from ~36° at the southwest end to ~83° at the northeast end of the rupture. (2) The fault rupture style changes from predominantly thrust at the southwest end to dextral at the northeast end of the fault rupture. (3) Fault slip peaks near the surface for most parts of the fault, with ~8.4 m thrust and ~5 m dextral slip near Hongkou and ~6 m thrust and ~8.4 m dextral slip near Beichuan, respectively. (4) The peak slips are located around fault geometric complexities, suggesting that earthquake style and rupture propagation were determined by fault zone geometric barriers. Such barriers exist primarily along restraining left stepping discontinuities of the dextral-compressional fault system. (5) The seismic moment released on the fault above 20 km depth is 8.2 x 10 21  N m, corresponding to an M w 7.9 event. The seismic moments released on the local slip concentrations are equivalent to events of M w 7.5 at Yingxiu-Hongkou, M w 7.3 at Beichuan-Pingtong, M w 7.2 near Qingping, M w 7.1 near Qingchuan, and M w 6.7 near Nanba, respectively. (6) The fault geometry and kinematics are consistent with a model in which crustal deformation at the eastern margin of the Tibetan plateau is decoupled by differential motion across a decollement in the mid crust, above which deformation is dominated by brittle reverse faulting and below which deformation occurs by viscous horizontal shortening and vertical thickening.
    Keywords: Seismology
    Print ISSN: 0956-540X
    Electronic ISSN: 1365-246X
    Topics: Geosciences
    Published by Oxford University Press on behalf of The Deutsche Geophysikalische Gesellschaft (DGG) and the Royal Astronomical Society (RAS).
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  • 4
    Publication Date: 2015-09-06
    Description: Recently constructed models of crustal structure across Tibet based on surface wave data display a prominent mid-crustal low velocity zone (LVZ) but are vertically smooth in the crust. Using six months of broad-band seismic data recorded at 22 stations arrayed approximately linearly over a 440 km observation profile across northeastern Tibet (from the Songpan–Ganzi block, through the Qaidam block, into the Qilian block), we perform a Bayesian Monte Carlo joint inversion of receiver function data with surface wave dispersion to address whether crustal layering is needed to fit both data sets simultaneously. On some intervals a vertically smooth crust is consistent with both data sets, but across most of the observation profile two types of layering are required: a discrete LVZ or high velocity zone (HVZ) formed by two discontinuities in the middle crust and a doublet Moho formed by two discontinuities from 45–50 km to 60–65 km depth connected by a linear velocity gradient in the lowermost crust. The final model possesses (1) a mid-crustal LVZ that extends from the Songpan–Ganzi block through the Kunlun suture into the Qaidam block consistent with partial melt and ductile flow and (2) a mid-crustal HVZ bracketing the south Qilian suture coincident with ultrahigh pressure metamorphic rocks at the surface. (3) Additionally, the model possesses a doublet Moho extending from the Qaidam to the Qilian blocks which probably reflects increased mafic content with depth in the lowermost crust perhaps caused by a vertical gradient of ecologitization. (4) Crustal thickness is consistent with a step-Moho that jumps discontinuously by 6 km from 63.8 km (±1.8 km) south of 35° to 57.8 km (±1.4 km) north of this point coincident with the northern terminus of the mid-crustal LVZ. These results are presented as a guide to future joint inversions across a much larger region of Tibet.
    Keywords: Seismology
    Print ISSN: 0956-540X
    Electronic ISSN: 1365-246X
    Topics: Geosciences
    Published by Oxford University Press on behalf of The Deutsche Geophysikalische Gesellschaft (DGG) and the Royal Astronomical Society (RAS).
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  • 5
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Supercritical fluid chromatography ; Solvating gas chromatography ; Polybutadiene coated zirconia ; CO2 mobile phase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In this paper, practical considerations of column efficiency, separation speed, thermal stability, and column polarity of capillary columns packed with polybutadiene-coated zirconia were investigated under solvating gas chromatography (SGC) conditions using carbon dioxide as mobile phase. When compared with results obtained from conventional porous octadecyl obtained from conventional porous octadecyl bonded silica (ODS) particles, PBD-zirconia particles produced greater change in mobile phase linear velocity with pressure than conventional ODS particles under the same conditions. The maximum plate number per second (Nt) obtained with a 30 cm PBD-zirconia column was approximately 1.5 times higher than that obtained with an ODS column at 100 °C. Therefore, the PBD-zirconia phase is more suitable for fast separations than conventional ODS particles in SGC. Maximum plate numbers per meter of 76,900 and 63,300 were obtained using a 57 cm×250 μm i.d. fused silica capillary column packed with 3 μm PBD-zirconia at 50 °C and 100 °C, respectively. The PBD-zirconia phase was stable at temperatures up to 320 °C under SGC conditions using carbon dioxide as mobile phase. Polarizable aromatic compounds and low molecular weight ketones and aldehydes were eluted with symmetrical peaks from a 10 cm column packed with 3 μm PBD-zirconia. Zirconia phases with greater inertness are required for the analysis of more polar compounds by SGC.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1612-1112
    Keywords: Supercritical fluid chromatography ; Packed capillary columns ; Liquid crystalline polysiloxane ; Polymer encapsulated particles ; Vitamins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Liquid crystal polysiloxane stationary phases were prepared by coating two different polymers on deactivated porous silica particles (10 μm diameter, 80 Å pores). Deactivation of the silica particles before coating was necessary to prepare highly efficient and inert stationary phases for supercritical fluid chromatography (SFC). Fat-soluble vitamins E, A, K1, K2, D2, and D3 were separated on these columns using neat supercritical CO2 as mobile phase. The analyses were completed within 40 min at 70 °C. The results were compared to those obtained using a capillary column packed with less ordered liquid crystalm,m-cyanobiphenyl-substituted polysiloxane coated particles. Reduced shape selectivity was observed with this cyanobiphenyl phase. The response factors of vitamins A, E, K1, K2, D2, and D3 when using the flame ionization detector (FID) were determined to be very similar.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1612-1112
    Keywords: Supercritical fluid chromatography ; Packed capillary columns ; Polyethylene oxide coated phases ; Polymer encapsulated particles ; Amines and acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Polyethylene oxide (PEO)-based polymers with hydroxy, methoxy, and aminopropoxy terminal groups were coated on diol functionalized and hexamethyldisilazane end-capped silica particles. Proton-donor and proton-acceptor test solutes, including carboxylic acids, hydroxy-containing compounds, arylamines, and alkylamines were used to evaluate the chromatographic performances of these polymer coated particles under SFC conditions with neat CO2 as mobile phase. It was found that the particles coated with hydroxy-terminated PEO were suitable for the separation of proton-donor compounds such as hydroxy-containing compounds and carboxylic acids, and the particles coated with aminopropoxy-terminated PEO could be used for the separation of amines. That is, the proton-accepting stationary phase is suitable for the separation of proton accepting solutes, including strong basic alkylamines (pKb≈4), using neat CO2 as mobile phase, while the protondonating stationary phase is suitable for the separation of proton-donating compounds such as carboxylic acids (pKa≈4). Hydrogen bond basicity was found to be a critical factor for the chromatography of basic amines. Low volatility acidic and basic drugs were chromatographed using the new stationary phases. The stability of the PEO coated particles was determined by measuring the loss of organic carbon under SFC conditions. It was found that approximately 18 % of the coating (average molecular weight of 15,000) was washed out of the particles by supercritical CO2 after 7 h at 350 atm and 50°C
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1612-1112
    Keywords: Solvating gas chromatography ; Supercritical fluid chromatography ; Packed capillary columns ; Solvating power
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The efficiency (plate number per unit time) and elution power (range ofn-alkanes) of packed capillary SFC and SGC using CO2 as the mobile phase were compared. A higher plate number per unit time was obtained in SGC than in SFC using the same column under the same applied conditions. SGC is more suitable for fast separations than SFC. The solvating ability of the mobile phase, at the column exit end, decreased remarkably after the restrictor was removed. However, the elution molecular weight range in SGC can be greatly extended by increasing the column temperature.n-Alkanes with carbon numbers as high as 80 were separated under SGC conditions using a 35 cm ×250 μm i.d. column packed with 10 μm polymer-encapsulated silica particles at 200 atm, with a temperature program of 100–380°C at 10°C min−1.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 49 (1999), S. 333-337 
    ISSN: 1612-1112
    Keywords: Supercritical fluid chromatography ; Gas chromatography ; Solvating gas chromatography ; Peak capacity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In this paper, a general peak capacity expression was evaluated using columns containing various packing materials under solvating gas chromatography (SGC) conditions. Differing from column efficiency, peak capacity can describe both separation capability and speed when introducing the dead time into the peak capacity expression. Various factors that influence peak capacity in SGC are described, including particle pore size, chemical surface modification, particle size, column length, temperature, and pressure.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1612-1112
    Keywords: Supercritical fluid chromatography ; Surface modification ; Deactivation ; Silica particles ; Stationary phases ; Packing materials ; Packed capillary columns
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Spherical porous silica particles (10 μm diameter, 300 Å and 80 Å pores), spherical nonporous silica particles (10 μm diameter), and irregular porous silica particles (≈10 μm diameter, 80 Å pores) were deactivated with polymethylhydrosiloxane (PS). The surface activities of the deactivated silica particles were investigated using various polar compounds under supercritical fluid chromatography (SFC) conditions (neat CO2), and compared with a commercial C18-bonded phase. The small pore (80 Å) silica particles could be more completely deactivated than larger pore (300 Å) and nonporous silica particles. The success of the PS deactivation method is ascribed to the excellent match between the reactive groups on the polymer backbone and the silica surface, and the formation of a highly crosslinked polymeric layer over the surface. Physical processes, such as adsorption and desorption of the deactivation reagent on the surface and diffusion from the surface, were found to have important effects on the deactivation. Using capillary columns packed with PS deactivated silica particles, typical polar organic compounds, including hydroxyl-containing compounds, carbonyl-containing compounds, free amines, and free carboxylic acids, were separated by SFC and compared with results from a commercial C18-bonded phase. While the results clearly show that the PS deactivated particles were more inert than the C18-bonded phase, better deactivation methods are still needed for separation of free acids and alkylamines.
    Type of Medium: Electronic Resource
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