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  • Other Sources  (149)
  • American Chemical Society
  • American Geophysical Union
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  • 1
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    American Geophysical Union
    In:  J. Geophys. Res., Washington, D.C., American Geophysical Union, vol. 97, no. 8, pp. 11995-12013, pp. 2340, (ISSN: 1340-4202)
    Publication Date: 1992
    Keywords: Stress ; Fault plane solution, focal mechanism ; 16 ; (Structural ; Geology) ; 18 ; (Geophysics, ; Solid ; Earth) ; JGR ; California ; tectonophysics ; crust ; Indonesia ; structural ; geology ; neotectonics ; faults ; displacements ; active ; faults ; Pacific ; Coast ; Western ; U.S. ; United ; States ; San ; Andreas ; Fault ; Far ; East ; Asia ; Sumatra ; strike-slip ; faults ; borehole ; breakouts ; earthquakes ; focal ; mechanism ; plate ; tectonics
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  • 2
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    American Geophysical Union
    In:  Washington, D.C., American Geophysical Union, vol. 1, (ISBN 0-521-81734-X)
    Publication Date: 1995
    Keywords: Handbook of mineralogy ; Rock mechanics ; Physical properties of rocks ; Handbook of physics ; Geochemistry
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  • 3
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    American Geophysical Union
    In:  London, American Geophysical Union, vol. 1, no. 3, pp. 632 pp., (ISBN-10: 1-84628-053-2, ISBN-13:978-1-84628-053-5, eISBN 1-84628-054-0, xx + 591 pp. + CD-ROM)
    Publication Date: 1994
    Keywords: Seismology ; GeodesyY ; Synthetic seismograms
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  • 4
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    American Geophysical Union
    In:  Washington, D.C., American Geophysical Union, vol. 6, no. 1, pp. 1-40, (ISBN: 0-444-51340-X)
    Publication Date: 1990
    Keywords: EUROPROBE (Geol. and Geophys. in eastern Europe) ; Handbook of geology ; Geol. aspects ; Plate tectonics
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  • 5
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    American Geophysical Union
    In:  Mineral Physics & Crystallography - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 37, pp. 64-97, (ISBN 3-540-24988-5)
    Publication Date: 1995
    Keywords: Laboratory measurements ; Physical properties of rocks ; Review article ; Mineralogy
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  • 6
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    American Geophysical Union
    In:  Professional Paper, Flow and Fracture of Rocks, Washington, D. C., American Geophysical Union, vol. 16, no. 16, pp. 109-115, (ISBN 0080419208)
    Publication Date: 1972
    Keywords: Fluids ; Physical properties of rocks ; Laboratory measurements ; Rock mechanics
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  • 7
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    American Geophysical Union
    In:  Professional Paper, Earthquake Source Mechanics, Washington, D.C., American Geophysical Union, vol. 37, no. 16, pp. 275-283, (ISBN 0080419208)
    Publication Date: 1986
    Keywords: Spectrum ; Source parameters ; Seismology
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  • 8
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    American Geophysical Union
    In:  Professional Paper, Flow and Fracture of Rocks, Washington, D. C., American Geophysical Union, vol. 16, no. 16, pp. 167-190, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1972
    Keywords: Physical properties of rocks ; Seismology ; Anisotropy ; earth mantle ; ConvolutionE
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  • 9
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    American Geophysical Union
    In:  Professional Paper, Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 24, no. 231, pp. 7-13, (ISBN: 3-540-23712-7)
    Publication Date: 1994
    Keywords: Modelling ; Earthquake precursor: prediction research ; Earthquake precursor: statistical anal. of seismicity ; criticality ; Review article ; Chaotic behaviour ; FractureT
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  • 10
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 1, pp. 126-143, (ISBN: 3-540-23712-7)
    Publication Date: 1995
    Keywords: Review article ; Seismology ; Travel time ; Handbook of geophysics
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  • 11
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 1, no. 4, pp. 1-5, (ISBN 0080419208)
    Publication Date: 1994
    Keywords: Review article ; Non-linear effects ; Chaotic behaviour
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  • 12
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    American Geophysical Union
    In:  Washington, D.C., American Geophysical Union, vol. 96, pp. 225, (ISBN 0-471-95596-5)
    Publication Date: 1990
    Keywords: Nuclear explosion ; Textbook of geophysics ; Review article
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  • 13
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    American Geophysical Union
    In:  Professional Paper, Rock Physics & Phase Relations - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 14, no. 16, pp. 1-7, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Physical properties of rocks ; Mineralogy ; Review article
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  • 14
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    American Geophysical Union
    In:  Professional Paper, Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 16, pp. 271-282, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Review article ; radioactivity ; Handbook of geophysics ; Handbook of physics
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  • 15
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    American Geophysical Union
    In:  Professional Paper, Flow and Fracture of Rocks, Washington, D. C., American Geophysical Union, vol. 16, no. 16, pp. 265-273, (ISBN 0080419208)
    Publication Date: 1972
    Keywords: Fluids ; Physical properties of rocks ; Rock mechanics ; Laboratory measurements
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  • 16
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    American Geophysical Union
    In:  Professional Paper, Rock Physics & Phase Relations - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 1002, no. 231, pp. 148-165, (ISBN 1-4020-1729-4)
    Publication Date: 1995
    Keywords: Rheology ; Inelastic ; Rock mechanics ; Physical properties of rocks ; Review article
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  • 17
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Flow and Fracture of Rocks, Washington, D. C., American Geophysical Union, vol. 16, no. XVI:, pp. 243-258, (ISBN: 3-540-23712-7)
    Publication Date: 1972
    Keywords: Rock mechanics ; Laboratory measurements ; Inelastic ; Physical properties of rocks
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  • 18
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Flow and Fracture of Rocks, Washington, D. C., American Geophysical Union, vol. 16, no. XVI:, pp. 29-53, (ISBN: 3-540-23712-7)
    Publication Date: 1972
    Keywords: Rheology ; Physical properties of rocks ; Inelastic ; Laboratory measurements ; Rock mechanics
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  • 19
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 4, pp. 88-103, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Review article ; Earth model, also for more shallow analyses ! ; Rheology ; Seismology
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  • 20
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 4, pp. 104-125, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Review article ; (The Earth's free) oscillations ; Attenuation ; Rheology
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  • 21
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    American Geophysical Union
    In:  Professional Paper, Open-File Rept., Rock Physics & Phase Relations - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 22, no. 16, pp. 20-34, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Physical properties of rocks ; Attenuation ; porosity ; Velocity ; Review article
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  • 22
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 10, no. 28, pp. 309-314
    Publication Date: 1995
    Keywords: Seismics (controlled source seismology) ; Deep seismic sounding (espec. cont. crust) ; Plate tectonics ; Review article
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  • 23
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    American Geophysical Union
    In:  Bull., Open-File Rept., Mineral Physics & Crystallography - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 24, no. 16, pp. 303-331, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1995
    Keywords: NMR ; Spectrum ; Spectral analysis ; Geochemistry ; Physical properties of rocks ; Review article
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  • 24
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    American Geophysical Union
    In:  Professional Paper, Open-File Rept., Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 16, pp. 283-291, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Review article ; radioactivity ; isotopes ; Geothermics
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  • 25
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    American Geophysical Union
    In:  Bull., Open-File Rept., Earthquake Source Mechanics, Washington, D.C., American Geophysical Union, vol. 37, no. 16, pp. 285-296, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1986
    Keywords: Seismology ; Seismic networks ; Fracture ; Source
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  • 26
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by, Washington, D.C., American Geophysical Union, vol. 10, no. 302, pp. 365-369
    Publication Date: 1995
    Keywords: Plate tectonics ; Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Seismicity ; Geodesy ; Review article
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  • 27
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    American Geophysical Union
    In:  Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, pp. 206-213
    Publication Date: 1995
    Keywords: Review article ; Seismology ; Magnitude ; Energy (of earthquakes) ; seismic Moment
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  • 28
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    American Geophysical Union
    In:  Earthquake Source Mechanics, Washington, D.C., American Geophysical Union, vol. 37, pp. 311-318, (ISBN 3-540-24988-5)
    Publication Date: 1986
    Keywords: Seismology ; Source ; Attenuation
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  • 29
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    American Geophysical Union
    In:  Professional Paper, Rock Physics & Phase Relations - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 1, no. 16, pp. 105-126, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1995
    Keywords: Geothermics ; Physical properties of rocks ; Review article
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  • 30
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. XVI:, pp. 190-205, (ISBN: 3-540-23712-7)
    Publication Date: 1995
    Keywords: Review article ; Geoelectrics ; Earth model, also for more shallow analyses !
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  • 31
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Earthquake Source Mechanics, Washington, D.C., American Geophysical Union, vol. 37, no. 16, pp. 269-274, (ISBN: 3-540-23712-7)
    Publication Date: 1986
    Keywords: Seismology ; Green's function ; Source
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  • 32
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Mineral Physics & Crystallography - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 3, no. 1, pp. 227-236, (ISBN: 3-540-23712-7)
    Publication Date: 1995
    Keywords: Rheology ; Inelastic ; Modelling ; Review article ; Geothermics ; Earth model, also for more shallow analyses !
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  • 33
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Flow and Fracture of Rocks, Washington, D. C., American Geophysical Union, vol. 16, no. 1, pp. 259-263, (ISBN: 3-540-23712-7)
    Publication Date: 1972
    Keywords: Modelling ; Aftershocks ; Seismology ; Seismicity
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  • 34
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 48, no. 4, pp. 37-41, (ISBN 0080419208)
    Publication Date: 1994
    Keywords: Dynamic ; Chaotic behaviour ; Non-linear effects
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  • 35
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    American Geophysical Union
    In:  Bull., Open-File Rept., U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994, Washington, D.C., American Geophysical Union, vol. 65, no. 1, pp. 23-40, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Review article ; Seismology ; Tectonics ; Plate tectonics ; Volcanology ; Earthquake hazard ; Earthquake precursor: prediction research ; Earth rotation ; Geochemistry ; Nuclear explosion ; Source ; Deep seismic sounding (espec. cont. crust) ; GeodesyY ; Chaotic behaviour ; Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Rock mechanics ; remote ; sensing ; Mineralogy ; Geodesy ; Global Positioning System ; Very Long Baseline Interferometry ; Satellite Laser Ranging ; Gravimetry, Gravitation ; Planetology
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  • 36
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    American Geophysical Union
    In:  Washington, D.C., American Geophysical Union, vol. 1, (ISBN 0-521-81734-X)
    Publication Date: 1995
    Keywords: Handbook of geophysics ; Rock mechanics ; Physical properties of rocks ; Handbook of physics
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  • 37
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    American Geophysical Union
    In:  Washington, American Geophysical Union, vol. 1, (ISBN 0-521-81734-X)
    Publication Date: 1995
    Keywords: Handbook of geophysics ; Plate tectonics ; TIDES ; Geomagnetics ; Geothermics ; Seismology ; Geoelectrics ; Earth model, also for more shallow analyses ! ; Gravimetry, Gravitation ; Paleomagnetism ; isotopes ; Geochemistry ; Oceanography ; Volcanology ; physical ; constants
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  • 38
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    American Geophysical Union
    In:  Washington, 107 pp., American Geophysical Union, vol. IUGG Volume 18, no. 85, pp. 799-804, (ISBN 3-540-23219-2)
    Publication Date: 1994
    Keywords: Non-linear effects ; FractureT ; Chaotic behaviour ; SOC ; criticality ; Textbook of geophysics ; Dynamic ; Earthquake precursor: prediction research
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  • 39
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    American Geophysical Union
    In:  Earthquake Source Mechanics, Washington, D.C., American Geophysical Union, vol. 37, pp. 259-267, (ISBN 3-540-24988-5)
    Publication Date: 1986
    Keywords: Seismology ; Source parameters ; Seismicity
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  • 40
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    American Geophysical Union
    In:  Earthquake Source Mechanics, Washington, D.C., American Geophysical Union, vol. 37, no. 16, pp. 195-207, (ISBN 0080419208)
    Publication Date: 1986
    Keywords: Source parameters ; Fault zone ; Inelastic ; Creep observations and analysis ; Source ; Earthquake precursor: prediction research
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  • 41
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    American Geophysical Union
    In:  Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 22, no. 16, pp. 69-74, (ISBN 0080419208)
    Publication Date: 1994
    Keywords: SOC ; Chaotic behaviour ; Non-linear effects ; Earthquake precursor: prediction research ; Earthquake precursor: statistical anal. of seismicity
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  • 42
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    American Geophysical Union
    In:  Mineral Physics & Crystallography - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 17, no. 16, pp. 303-331, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Mineralogy ; Physical properties of rocks ; Review article
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  • 43
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    American Geophysical Union
    In:  Professional Paper, Properties and Processes of the Earth's Lower Crust, Oxford, American Geophysical Union, vol. 54, no. 16, pp. 197-213, (ISBN 1-4020-1729-4)
    Publication Date: 1989
    Keywords: CRUST ; Geothermics ; Inelastic ; Muller
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  • 44
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    American Geophysical Union
    In:  Professional Paper, Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 16, pp. 66-87, (ISBN: 3-540-23712-7)
    Publication Date: 1995
    Keywords: Plate tectonics ; Modelling ; Review article ; Geodesy ; Paleomagnetism
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  • 45
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    American Geophysical Union
    In:  Professional Paper, Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 65, no. 16, pp. 15-35, (ISBN: 3-540-23712-7)
    Publication Date: 1994
    Keywords: Non-linear effects ; Friction ; Fracture ; Physical properties of rocks
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  • 46
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    American Geophysical Union
    In:  Bull., Polar Proj. OP-O3A4, Rock Physics & Phase Relations - A Handbook of Physical Constants, Washington, D.C., American Geophysical Union, vol. 1, no. 4, pp. 127-147, (ISBN 0080419208)
    Publication Date: 1995
    Keywords: Rock mechanics ; Geochemistry ; Physical properties of rocks ; Mineralogy ; Review article
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  • 47
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    American Geophysical Union
    In:  Professional Paper, Open-File Rept., Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 4, no. 2, pp. 55-60, (ISBN 0080419208)
    Publication Date: 1994
    Keywords: Earthquake precursor: prediction research ; Non-linear effects ; Earthquake precursor: stresses ; Modelling ; Stress
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  • 48
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 10, no. SC.TECH./SEM.16/R.60, pp. 299-308
    Publication Date: 1995
    Keywords: Source ; Modelling ; Seismology ; Review article
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  • 49
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 10, no. SC.TECH./SEM.16/R.60, pp. 379-383
    Publication Date: 1995
    Keywords: Tectonics ; rifting ; basins ; Fault zone ; Stress ; Fluids ; Review article
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  • 50
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. C 560, 183 pp., no. M79-E-11 [79127 Arto 129], pp. 249-255, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Earthquake hazard ; Review article
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  • 51
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. C 560, 183 pp., no. PL-TR-91-2097, pp. 371-377, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Geodesy ; Very Long Baseline Interferometry ; Satellite Laser Ranging ; Global Positioning System ; Plate tectonics ; Review article
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  • 52
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. C 560, 183 pp., no. 25, pp. 287-297, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Seismology ; Source ; Mineralogy ; Hypocentral depth ; Review article
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  • 53
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. C 560, 183 pp., no. AFGL-TR-88-0314, pp. 413-418, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Plate tectonics ; evolution ; GeodesyY ; Review article
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  • 54
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 10, no. paper SPWLA 90-H, pp. 257-262, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Volcanology ; Earthquake precursor: prediction research ; Earthquake hazard ; Review article
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  • 55
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 10, no. 89-144, pp. 269-273, (ISBN 0 08 042822 3)
    Publication Date: 1995
    Keywords: Seismology ; Nuclear explosion ; Review article
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  • 56
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. C 560, 183 pp., no. 57, pp. 451-457, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Rock mechanics ; Rheology ; Review article
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  • 57
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 1034, no. SAND 80-2048, pp. 283-286, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Source ; Seismology ; Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Energy (of earthquakes) ; Review article
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  • 58
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. C 560, 183 pp., no. 70, pp. 263-267, (ISBN 3-933346-037)
    Publication Date: 1995
    Keywords: Volcanology ; Earthquake hazard ; Seismology ; Review article
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  • 59
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, vol. 10, no. 91-N-FA07-7-4, pp. 341-343, (ISBN 0 08 042822 3)
    Publication Date: 1995
    Keywords: Chaotic behaviour ; FractureT ; Non-linear effects ; Review article
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  • 60
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    American Geophysical Union
    In:  Professional Paper, Open-File Rept., Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 3, no. 16, pp. 43-53, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1994
    Keywords: Earthquake ; Dynamic ; Seismicity ; Hypocentral depth
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  • 61
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    American Geophysical Union
    In:  Professional Paper, Open-File Rept., Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 4, no. 2, pp. 75-80, (ISBN 0080419208)
    Publication Date: 1994
    Keywords: Chaotic behaviour ; Friction
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  • 62
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    American Geophysical Union
    In:  U.S. National Report to International Union of Geodesy and Geophysics 1991 - 1994. Contributions in Dynamics of the Solid Earth and Other Planets, ed. by R. A. Pielke, Washington, D.C., American Geophysical Union, no. 43, pp. 243-247
    Publication Date: 1995
    Keywords: Earthquake precursor: prediction research ; Earthquake risk ; Review article
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  • 63
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    American Geophysical Union
    In:  Bull., Open-File Rept., Nonlinear Dynamics and Predictability of Geophysical Phenomena, Washington, American Geophysical Union, vol. 5, no. 16, pp. 81-89, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1994
    Keywords: Modelling ; Earthquake precursor: prediction research ; Earthquake precursor: models ; Chaotic behaviour
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  • 64
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    American Geophysical Union
    In:  Bull., Open-File Rept., Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 16, pp. 144-158, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1995
    Keywords: Geothermics ; Review article
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  • 65
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    American Geophysical Union
    In:  Bull., Open-File Rept., Global Earth Physics: A Handbook of Physical Constants, Washington, American Geophysical Union, vol. 1, no. 1, pp. 214-224, (ISBN 1-86239-165-3, vi + 330 pp.)
    Publication Date: 1995
    Keywords: Review article ; Velocity depth profile ; Earth model, also for more shallow analyses ! ; Deep seismic sounding (espec. cont. crust)
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  • 66
    Publication Date: 2020-07-16
    Description: Microbial mats collected at cold methane seeps in the Black Sea carry out anaerobic oxidation of methane (AOM) to carbon dioxide using sulfate as the electron acceptor. These mats, which predominantly consist of sulfate-reducing bacteria and archaea of the ANME-1 and ANME-2 type, contain large amounts of proteins very similar to methyl-coenzyme M reductase from methanogenic archaea. Mass spectrometry of mat samples revealed the presence of two nickel-containing cofactors in comparable amounts, one with the same mass as coenzyme F430 from methanogens (m/z = 905) and one with a mass that is 46 Da higher (m/z = 951). The two cofactors were isolated and purified, and their constitution and absolute configuration were determined. The cofactor with m/z = 905 was proven to be identical to coenzyme F430 from methanogens. For the m/z = 951 species, high resolution ICP-MS pointed to F430 + CH2S as the molecular formula, and LA-ICP-SF MS finally confirmed the presence of one sulfur atom per nickel. Esterification gave two stereoisomeric pentamethyl esters with m/z = 1021, which could be purified by reverse phase HPLC and were subjected to comprehensive NMR analysis, allowing determination of their constitution and configuration as (172S)−172-methylthio-F430 pentamethyl ester and (172R)−172-methylthio-F430 pentamethyl ester. The corresponding diastereoisomeric pentaacids could also be separated by HPLC and were correlated to the esters via mild hydrolysis of the latter. Equilibration of the pentaacids under acid catalysis showed that the (172S) isomer is the naturally occurring albeit thermodynamically less stable one. The more stable (172R) isomer (80% at equilibrium) is an isolation artifact generated under the acidic conditions necessary for the isolation of the cofactors from the calcium carbonate-encrusted mats.
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  • 67
    Publication Date: 2017-11-20
    Description: Marine methane hydrate in sands has huge potential as an unconventional gas resource; however, no field test of their production potential had been conducted. Here, we report the world’s first offshore methane hydrate production test conducted at the eastern Nankai Trough and show key findings toward future commercial production. Geological analysis indicates that hydrate saturation reaches 80% and permeability in the presence of hydrate ranges from 0.01 to 10 mdarcies. Permeable (1–10 mdarcies) highly hydrate-saturated layers enable depressurization-induced gas production of approximately 20,000 Sm3/D with water of 200 m3/D. Numerical analysis reveals that the dissociation zone expands laterally 25 m at the front after 6 days. Gas rate is expected to increase with time, owing to the expansion of the dissociation zone. It is found that permeable highly hydrate-saturated layers increase the gas–water ratio of the production fluid. The identification of such layers is critically important to increase the energy efficiency and the technical feasibility of depressurization-induced gas production from hydrate reservoirs.
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  • 68
    Publication Date: 2020-05-11
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  • 69
    Publication Date: 2020-07-20
    Description: The guest-exchange method (or replacement) for methane production from gas hydrates has recently received attention because it can be used for both carbon dioxide sequestration and methane production. The structure of gas hydrates is maintained as a structure I (sI) hydrate while methane molecules are exchanged with carbon dioxide. In this study, CH4 + CO2 mixed gas hydrates were examined under terahertz light at various temperatures to simulate CH4–CO2 exchange reactions. Each gas hydrate composition examined was a representative composition at each step of the exchange reaction. The molecular composition was also accurately analyzed by gas chromatography. Refractive indices calculated by the terahertz time-domain spectroscopy (THz-TDS) of gas hydrate samples were correlated to the guest composition, and this novel method was proven to be used to quantify the extent of replacement via optical constant. Furthermore, changes in the water framework from the sI hydrate to ice using THz-TDS were investigated with an increasing temperature. Overall, this study reveals the process of guest exchange and phase transition from a gas hydrate to ice via the optical properties in the terahertz region, and it offers a powerful tool in gas hydrate production.
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  • 70
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    American Chemical Society
    In:  The Journal of Physical Chemistry A, 115 (46). pp. 13324-13331.
    Publication Date: 2020-05-11
    Description: Microscopy, confocal Raman spectroscopy and powder X-ray diffraction (PXRD) were used for in situ investigations of the CO2-hydrocarbon exchange process in gas hydrates and its driving forces. The study comprises the exposure of simple structure I CH4 hydrate and mixed structure II CH4–C2H6 and CH4–C3H8 hydrates to gaseous CO2 as well as the reverse reaction, i.e., the conversion of CO2-rich structure I hydrate into structure II mixed hydrate. In the case of CH4–C3H8 hydrates, a conversion in the presence of gaseous CO2 from a supposedly more stable structure II hydrate to a less stable structure I CO2-rich hydrate was observed. PXRD data show that the reverse process requires longer initiation times, and structural changes seem to be less complete. Generally, the exchange process can be described as a decomposition and reformation process, in terms of a rearrangement of molecules, and is primarily induced by the chemical potential gradient between hydrate phase and the provided gas phase. The results show furthermore the dependency of the conversion rate on the surface area of the hydrate phase, the thermodynamic stability of the original and resulting hydrate phase, as well as the mobility of guest molecules and formation kinetics of the resulting hydrate phase.
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  • 71
    Publication Date: 2020-07-27
    Description: In the colloidal synthesis of iron sulfides, a series of dialkyl disulfides, alkyl thiols, and dialkyl disulfides (allyl, benzyl, tert-butyl, and phenyl) were employed as sulfur sources. Their reactivity was found to tune the phase between pyrite (FeS2), greigite (Fe3S4), and pyrrhotite (Fe7S8). DFT was used to show that sulfur-rich phases were favored when the C–S bond strength was low in the organosulfurs, yet temperature dependent studies and other observations indicated the reasons for phase selectivity were more nuanced; the different precursors decomposed through different reaction mechanisms, some involving the oleylamine solvent. The formation of pyrite from diallyl disulfide was carefully studied as it was the only precursor to yield FeS2. Raman spectroscopy indicated that FeS2 forms directly without an FeS intermediate, unlike most synthetic procedures to pyrite. Diallyl disulfide releases persulfide (S–S)2– due to the lower C–S bond strength relative to the S–S bond strength, as well as facile decomposition in the presence of amines through SN2′ mechanisms at elevated temperatures.
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  • 72
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    American Chemical Society
    In:  ACS Division of Fuel Chemistry Preprints, 42 (2). pp. 544-547.
    Publication Date: 2018-04-11
    Description: Test specimens of methane hydrate were grown under static conditions by combining cold, pressurized CH4 gas with H2O ice grains, then warming the system to promote the reaction CH4 (g) + 6H2O (s???l) ??? CH4??6H2O. Hydrate formation evidently occurs at the nascent ice/liquid water interface, and complete reaction was achieved by warming the system above 271.5 K and up to 289 K, at 25-30 MPa, for approximately 8 hours. The resulting material is pure methane hydrate with controlled grain size and random texture. Fabrication conditions placed the H2O ice well above its melting temperature before reaction completed, yet samples and run records showed no evidence for bulk melting of the ice grains. Control experiments using Ne, a non-hydrate-forming gas, verified that under otherwise identical conditions, the pressure reduction and latent heat associated with ice melting is easily detectable in our fabrication apparatus. These results suggest that under hydrate-forming conditions, H2O ice can persist metastably at temperatures well above its melting point. Methane hydrate samples were then tested in constant-strain-rate deformation experiments at T= 140-200 K, Pc= 50-100 MPa, and ????= 10-4-10-6 s-1. Measurements in both the brittle and ductile fields showed that methane hydrate has measurably different strength than H2O ice, and work hardens to a higher degree compared to other ices as well as to most metals and ceramics at high homologous temperatures. This work hardening may be related to a changing stoichiometry under pressure during plastic deformation; x-ray analyses showed that methane hydrate undergoes a process of solid-state disproportionation or exsolution during deformation at conditions well within its conventional stability field.
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  • 73
    Publication Date: 2020-06-15
    Description: Stable isotopic values on planktonic foraminifera in a suite of cores from basins across the SE Baffin Shelf are used to extract a record of meltwater events during Termination I deglaciation. Resolution and Hatton basins lie on the SE Baffin Shelf at water depths 〉 500 m, seaward of major conduits for ice drainage from the eastern sector of the Laurentide Ice Sheet (LIS). Accelerator mass spectrometry 14C dates are used to constrain our chronology of events in ten cores. In Resolution Basin, three cores have 14C AMS dates on foraminifera of 〉 20 ka at their bases; whereas Hatton Basin cores terminate in sediments 〈 13 kyr. Sedimentation rates varied between 0.1 to 4.5 m/ka. Stable oxygen and carbon isotopic ratios were obtained on 146 samples of the planktonic foraminifera Neogloboquadrina pachyderma (Ehrenberg) sinistral, from seven of the ten cores. No evidence was found to indicate that test morphology or size affected ∂18O. Between 7 and 13.5 ka the surface water on the shelf was on average 1 ‰ lower than the open ocean signal. Significant temporal variations were found in both ∂18O and ∂13C. Evidence for significant low ∂18O events occurred between 13 and 8 ka. The ∂13C record from the planktonic foraminifera suggests a threefold division of events between 13 and 7 ka, with positive values between 10.8 and 13.0 ka, negative values between 9 and 10.8 ka, and positive values from 7 to 9 ka. The ∂18O data suggest the presence of meltwater on the shelf some 3,000 years prior to the first late glacial dates on terrestrial deglaciation (at circa 10.4 ka). “Hudson Strait must be the real key to the importance of the calving process during deglaciation, because it is potentially the largest marine outlet for the Laurentide Ice Sheet and because it leads into the very center of the ice sheet.....the rates of calving through Hudson Strait during the period of initial ∂18O rise unfortunately are unknown.”
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  • 74
    facet.materialart.
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    American Chemical Society
    In:  The Journal of Organic Chemistry, 63 (26). pp. 10011-10014.
    Publication Date: 2020-05-11
    Type: Article , PeerReviewed
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  • 75
    Publication Date: 2018-04-11
    Description: We describe a new and efficient technique to grow aggregates of pure methane hydrate in quantities suitable for physical and material properties testing. Test specimens were grown under static conditions by combining cold, pressurized CH4 gas with granulated H2O ice, and then warming the reactants to promote the reaction CH4(g) + 6H2O(s→l) → CH4·6H2O (methane hydrate). Hydrate formation evidently occurs at the nascent ice/liquid water interface on ice grain surfaces, and complete reaction was achieved by warming the system above the ice melting point and up to 290 K, at 25−30 MPa, for approximately 8 h. The resulting material is pure, cohesive, polycrystalline methane hydrate with controlled grain size and random orientation. Synthesis conditions placed the H2O ice well above its melting temperature while reaction progressed, yet samples and run records showed no evidence for bulk melting of the unreacted portions of ice grains. Control experiments using Ne, a non-hydrate-forming gas, showed that under otherwise identical conditions, the pressure reduction and latent heat associated with ice melting are easily detectable in our fabrication apparatus. These results suggest that under hydrate-forming conditions, H2O ice can persist metastably to temperatures well above its ordinary melting point while reacting to form hydrate. Direct observations of the hydrate growth process in a small, high-pressure optical cell verified these conclusions and revealed additional details of the hydrate growth process. Methane hydrate samples were then tested in constant-strain-rate deformation experiments at T = 140−200 K, Pc = 50−100 MPa, and ε = 10-4−10-6 s-1. Measurements in both the brittle and ductile fields showed that methane hydrate has measurably different strength than H2O ice, and work hardens to an unusually high degree compared to other ices as well as to most metals and ceramics at high homologous temperatures. This work hardening may be related to a changing stoichiometry under pressure during plastic deformation; X-ray analyses showed that methane hydrate undergoes a process of solid-state disproportionation or exsolution during deformation at conditions well within its conventional stability field.
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  • 76
    Publication Date: 2020-07-31
    Description: Numerical tools are essential for the prediction and evaluation of conventional hydrocarbon reservoir performance. Gas hydrates represent a vast natural resource with a significant energy potential. The numerical codes/tools describing processes involved during the dissociation (induced by several methods) for gas production from hydrates are powerful, but they need validation by comparison to empirical data to instill con fidence in their predictions. In this study, we successfully reproduce experimental data of hydrate dissociation using the TOUGH+HYDRATE (T+H) code. Methane(CH4)hydrate growth and dissociation in partially water- and gas-saturated Bentheim sandstone were spatially resolved using Magnetic Resonance Imaging (MRI), which allows the in situ monitoring of saturation and phase transitions. All the CH4 that had been initially converted to gas hydrate was recovered during depressurization. The physical system was reproduced numerically, usingboth a simplified 2D model and a 3D grid involving complex Voronoi elements. We modeled dissociation using both the equilibrium and the kinetic reaction options in T+H, and we used a range of kinetic parameters for sensitivity analysis and curve fitting. We successfully reproduced the experimental results, which confirmed the empirical data that demonstrated that heattransport was the limiting factor during dissociation. Dissociation was more sensitive to kinetic parameters than anticipated, which indicates that kinetic limitations may be important in short-term core studies and a necessity in such simulations. This is the first time T+H has been used to predict empirical nonmonotonic dissociation behavior, where hydrate dissociation and reformation occurred as parallel events.
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  • 77
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    American Chemical Society
    In:  Industrial & Engineering Chemistry Research, 49 (11). pp. 5231-5245.
    Publication Date: 2020-07-29
    Description: Methane hydrate, a potential future energy resource, is known to occur naturally in vast quantities beneath the ocean floor and in permafrost regions. It is important to evaluate how much methane is recoverable from these hydrate reserves. This article introduces the theoretical background of HydrateResSim, the National Energy Technology Laboratory (NETL) methane production simulator for hydrate-containing reservoirs, originally developed for NETL by Lawrence Berkeley National Laboratory (LBNL). It describes the mathematical model that governs the dissociation of methane hydrate by depressurization or thermal stimulation of the system, including the transport of multiple temperature-dependent components in multiple phases through a porous medium. The model equations are obtained by incorporating the multiphase Darcy’s law for gas and liquid into both the mass component balances and the energy conservation equations. Two submodels in HydrateResSim for hydrate dissociation are also considered: a kinetic model and a pure thermodynamic model. Contrary to more traditional reservoir simulations, the set of model unknowns or primary variables in HydrateResSim changes throughout the simulation as a result of the formation or dissociation of ice and hydrate phases during the simulation. The primary variable switch method (PVSM) is used to effectively track these phase changes. The equations are solved by utilizing the implicit time finite-difference method on the grid system, which can properly describe phase appearance or disappearance as well as the boundary conditions. The Newton-Raphson method is used to solve the linear equations after discretization and setup of the Jacobian matrix. We report here the application of HydrateResSim to a three-component, four-phase flow system in order to predict the methane produced from a laboratory-scale reservoir. The first results of HydrateResSim code in a peer-reviewed publication are presented in this article. The numerical solution was verified against the state-of-the art simulator TOUGH+Hydrate. The model was then used to compare twodissociation theories: kinetic and pure equilibrium. Generally, the kinetic model revealed a lower dissociation rate than the equilibrium model. The hydrate dissociation patterns differed significantly when the thermal boundary condition was shifted from adiabatic to constant-temperature. The surface area factor was found to have an important effect on the rate of hydrate dissociation for the kinetic model. The deviation between the kinetic and equilibrium models was found to increase with decreasing surface area factor.
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  • 78
    Publication Date: 2020-06-15
    Description: In the North Atlantic we define H-0 as a Heinrich-like event which occurred during the Younger Dryas chron. On the SE Baffin shelf prior to 11 ka, surface water productivity was reasonably high, as measured by the numbers of diatom and planktic foraminifera per gram, but an abrupt increase in detrital carbonate (DC-0 event) (from approximately 15% up to 50% carbonate by weight) occurred at 11 ± 14C ka and continued to circa 10 ka. These deposits, 2–6 m thick, are dominated by detrital calcite and silt- and clay-sized sediments. During this event (DC-0/H-0), ice extended onto the inner shelf but did not reach the shelf break and probably originated from a center over Labrador-Ungava. As a consequence, the pattern of ice-rafted debris and sediment provenance shown by H-O in the North Atlantic is different from that during H-1 (14.5 ka) or H-2 (20 ka) when the ice sheet extended along the axis of Hudson Strait and may have reached the shelf break; for example, there is no concrete evidence for DC-O is cores on the floor of the Labrador Sea due east of Hudson Strait (HU75-55,-56), but H-O has been noted in cores off Newfoundland and west of Ireland. A coeval carbonate event to DC-0, but this one dominated by dolomite, occurs in HU82-SU5 on the west side of Davis Strait with a source either from northern Baffin Bay or Cumberland Sound. Although other sources for North Atlantic detrital carbonate cannot be totally excluded, our evidence suggests that H-0 represents the expression of glaciological instability of the Laurentide Ice Sheet within the general region of Hudson Strait and probably to the north (Cumberland Sound and northernmost Baffin Bay). There is one younger DC event, dated circa 8.4 ka, present in sediments along the Labrador margin and in Hudson Strait, which represents the final collapse of the ice sheet within Hudson Strait and Hudson Bay.
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  • 79
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    American Chemical Society
    In:  Journal of Natural Products, 68 (5). pp. 759-761.
    Publication Date: 2020-07-21
    Description: Two new cyclic peroxides, 2 and 3, were isolated from a sample of the Norwegian sponge Plakortis simplex. Their structures including relative stereochemistry were elucidated by interpretation of MS and NMR data. Compound 3 exhibited moderate in vitro activity against six solid human tumor cell lines with IC50 values in the range 7−15 μg/mL.
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  • 80
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    American Chemical Society
    In:  The Journal of Physical Chemistry A, 107 (7). pp. 1050-1054.
    Publication Date: 2020-05-11
    Description: We determined the coordination environment of Zn2+ in aqueous Cl- brines at 25 °C and 300 °C using ab initio molecular dynamics simulations. The ZnCl+ and ZnCl2 complexes exist as pseudo-octahedral ZnClm(H2O)6-m clusters at 25 °C but occur as pseudo-tetrahedral ZnClm(H2O)4-m clusters at 300 °C. The ZnCl3- complex occurs as the pseudo-tetrahedral ZnCl3(H2O)- cluster at 25 and 300 °C. The tetrahedral ZnCl42- complex, however, is the dominant Zn−Cl complex at 25 °C, at least in highly concentrated (7.4 m) Cl- brines. The change in hydration number with temperature for the ZnCl+ and ZnCl2 complexes will complicate extrapolations of solvation energies to hydrothermal conditions using a Born-model-based equation of state.
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  • 81
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    American Chemical Society
    In:  Journal of Organic Chemistry, 66 (4). pp. 1210-1215.
    Publication Date: 2020-07-20
    Description: The valuable nutraceutical γ-linolenic acid (GLA, (6Z,9Z,12Z)-octadecatrienoic acid) is biosynthesized by a series of regio- and stereoselective dehydrogenation reactions that are catalyzed by a set of enzymes known as fatty acid desaturases. As part of ongoing research into the mechanism of these remarkable catalysts, we have examined the cryptoregiochemistry (site of initial oxidation) of Δ6 desaturation as it occurs in the protozoan Tetrahymena thermophila. Two complementary approaches that address this issue are described. In the first set of experiments, we measured the individual primary deuterium kinetic isotope effects associated with the C−H bond cleavages at C-6 and C-7. Competition experiments using appropriately deuterium-labeled 4-thiasubstrates revealed that a large KIE (kH/kD = 7.1 ± 0.5) was observed for the C−H bond-breaking step at C-6, whereas the C−H bond cleavage at C-7 was insensitive to deuterium substitution (kH/kD = 1.04 ± 0.05). These results point to C-6 as the site of initial oxidation in Δ6 desaturation since the first chemical step in this type of reaction is rupture of a strong, unactivated C−H bond, an energetically difficult process that typically exhibits a large KIE. This conclusion was supported by the results of our second approach, which involved locating the position of the putative diiron oxo oxidant with respect to substrate by monitoring the efficiency of oxo transfer to a series of thia fatty acid probes. Thus only a 6-thia-analogue is converted to significant amounts of the corresponding sulfoxide (9% yield). The absolute configuration of this product was determined to be S using (S)-MPAA as a chiral shift reagent. Taken together, these results point to the abstraction of the C-6 pro S hydrogen as the initial event in Δ6 desaturation as it occurs in T. thermophila.
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  • 82
    Publication Date: 2020-05-11
    Description: Calculations of the size and density of atmospheric aerosols are complicated by the fact that they can exist at concentrations highly supersaturated with respect to dissolved salts and supercooled with respect to ice. Densities and apparent molar volumes of solutes in aqueous solutions containing the solutes H2SO4, HNO3, HCl, Na2SO4, NaNO3, NaCl, (NH4)2SO4, NH4NO3, and NH4Cl have been critically evaluated and represented using fitted equations from 0 to 50 °C or greater and from infinite dilution to concentrations saturated or supersaturated with respect to the dissolved salts. Using extrapolated densities of high-temperature solutions and melts, the relationship between density and concentration is extended to the hypothetical pure liquid solutes. Above a given reference concentration of a few mol kg−1, it is observed that density increases almost linearly with decreasing temperature, and comparisons with available data below 0 °C suggest that the fitted equations for density can be extrapolated to very low temperatures. As concentration is decreased below the reference concentration, the variation of density with temperature tends to that of water (which decreases as temperature is reduced below 3.98 °C). In this region below the reference concentration, and below 0 °C, densities are calculated using extrapolated apparent molar volumes which are constrained to agree at the reference concentrations with an equation for the directly fitted density. Calculated volume properties agree well with available data at low temperatures, for both concentrated and dilute solutions. Comparisons are made with literature data for temperatures of maximum density. Apparent molar volumes at infinite dilution are consistent, on a single ion basis, to better than ±0.1 cm3 mol−1 from 0 to 50 °C. Volume properties of aqueous NaHSO4, NaOH, and NH3 have also been evaluated, at 25 °C only. In part 2 of this work (ref 1) an ion interaction (Pitzer) model has been used to calculate apparent molar volumes of H2SO4 in 0−3 mol kg−1 aqueous solutions of the pure acid and to represent directly the effect of the HSO4− ↔ H+ + SO42− reaction. The results are incorporated into the treatment of aqueous H2SO4 density described here. Densities and apparent molar volumes from −20 to 50 °C, and from 0 to 100 wt % of solute, are tabulated for the electrolytes listed in the title and have also been incorporated into the extended aerosol inorganics model (E-AIM, http://www.aim.env.uea.ac.uk/aim/aim.php) together with densities of the solid salts and hydrates.
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  • 83
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    American Chemical Society
    In:  Abstracts of Papers of the American Chemical Society, 243 . 536-ENVR.
    Publication Date: 2017-10-24
    Type: Article , NonPeerReviewed
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  • 84
    Publication Date: 2017-05-30
    Description: High-performance liquid chromatography-electrospray ionization mass spectrometry was applied to the detection of the iron(III) complexes of the hydroxamate siderophores rhodotoluric acid, deferrioxamine B, and deferrichrome. Separation of the iron(III) complexes was obtained using a polystyrene-divinylbenzene stationary phase. The retention and responses of ferrioxamine and ferrichrome were optimal when a gradient elution program with methanol and 0.1% (v/v) formic acid as the mobile phases was used. These conditions were also suitable for the retention and separation of the uncomplexed ligands. Retention of iron(III) rhodotoluate was improved when formic acid was replaced by the ion-pairing reagent heptafluorobutyric acid (0.1%). Detection limits for the ferric complexes, defined as 3 SD of the lowest determined standard, were 26 nM for iron(III) rhodotoluate, 0.23 nM for ferrioxamine, and 0.40 nM for ferrichrome. A protocol for the solid-phase extraction of these hydroxamate siderophores from seawater was developed and applied to the extraction of siderophores from enriched incubated seawater samples.
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  • 85
    Publication Date: 2017-05-30
    Description: High-performance liquid chromatography-electrospray ionization mass spectrometry was applied to the detection of the iron(III) complexes of the hydroxamate siderophores rhodotoluric acid, deferrioxamine B, and deferrichrome. Separation of the iron(III) complexes was obtained using a polystyrene-divinylbenzene stationary phase. The retention and responses of ferrioxamine and ferrichrome were optimal when a gradient elution program with methanol and 0.1% (v/v) formic acid as the mobile phases was used. These conditions were also suitable for the retention and separation of the uncomplexed ligands. Retention of iron(III) rhodotoluate was improved when formic acid was replaced by the ion-pairing reagent heptafluorobutyric acid (0.1%). Detection limits for the ferric complexes, defined as 3 SD of the lowest determined standard, were 26 nM for iron(III) rhodotoluate, 0.23 nM for ferrioxamine, and 0.40 nM for ferrichrome. A protocol for the solid-phase extraction of these hydroxamate siderophores from seawater was developed and applied to the extraction of siderophores from enriched incubated seawater samples.
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  • 86
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    Unknown
    American Chemical Society
    In:  Journal of Agricultural and Food Chemistry, 59 (18). pp. 9916-9921.
    Publication Date: 2020-07-27
    Description: A total of 19 naturally occurring bromophenols, with six new and 13 known structures, were isolated and identified from the methanolic extract of the marine red alga Rhodomela confervoides. The new compounds were identified by spectroscopic methods as 3,4-dibromo-5-((methylsulfonyl)methyl)benzene-1,2-diol (1), 3,4-dibromo-5-((2,3-dihydroxypropoxy)methyl)benzene-1,2-diol (2), 5-(aminomethyl)-3,4-dibromobenzene-1,2-diol (3), 2-(2,3-dibromo-4,5-dihydroxyphenyl)acetic acid (4), 2-methoxy-3-bromo-5-hydroxymethylphenol (5), and (E)-4-(2-bromo-4,5-dihydroxyphenyl)but-3-en-2-one (6). Each compound was evaluated for free radical scavenging activity against DPPH (α,α-diphenyl-β-dipicrylhydrazyl) and ABTS [2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid)diammonium salt] radicals. Most of them exhibited potent activities stronger than or comparable to the positive controls butylated hydroxytoluene (BHT) and ascorbic acid. The results from this study suggest that R. confervoides is an excellent source of natural antioxidants, and inclusion of these antioxidant-rich algal components would likely help prevent the oxidative deterioration of food.
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  • 87
    Publication Date: 2020-04-23
    Description: Implantable endovascular devices such as bare metal, drug eluting, and bioresorbable stents have transformed interventional care by providing continuous structural and mechanical support to many peripheral, neural, and coronary arteries affected by blockage. Although effective in achieving immediate restoration of blood flow, the long-term re-endothelialization and inflammation induced by mechanical stents are difficult to diagnose or treat. Here we present nanomaterial designs and integration strategies for the bioresorbable electronic stent with drug-infused functionalized nanoparticles to enable flow sensing, temperature monitoring, data storage, wireless power/data transmission, inflammation suppression, localized drug delivery, and hyperthermia therapy. In vivo and ex vivo animal experiments as well as in vitro cell studies demonstrate the previously unrecognized potential for bioresorbable electronic implants coupled with bioinert therapeutic nanoparticles in the endovascular system.
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  • 88
    Publication Date: 2020-04-23
    Description: The current difficulty in visualizing the true extent of malignant brain tumors during surgical resection represents one of the major reasons for the poor prognosis of brain tumor patients. Here, we evaluated the ability of a hand-held Raman scanner, guided by surface-enhanced Raman scattering (SERS) nanoparticles, to identify the microscopic tumor extent in a genetically engineered RCAS/tv-a glioblastoma mouse model. In a simulated intraoperative scenario, we tested both a static Raman imaging device and a mobile, hand-held Raman scanner. We show that SERS image-guided resection is more accurate than resection using white light visualization alone. Both methods complemented each other, and correlation with histology showed that SERS nanoparticles accurately outlined the extent of the tumors. Importantly, the hand-held Raman probe not only allowed near real-time scanning, but also detected additional microscopic foci of cancer in the resection bed that were not seen on static SERS images and would otherwise have been missed. This technology has a strong potential for clinical translation because it uses inert gold-silica SERS nanoparticles and a hand-held Raman scanner that can guide brain tumor resection in the operating room.
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  • 89
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    American Chemical Society
    In:  Energy & Fuels, 29 (9). pp. 5681-5691.
    Publication Date: 2020-07-31
    Description: The shrinking-core model of the formation of gas hydrates from ice spheres with well-defined geometry gives experimental access to the gas permeation in bulk hydrates which is relevant to their use as energy storage materials, their exploitation from natural resources, as well as to their role in flow assurance. Here we report on a new approach to model CO2 clathration experiments in the temperature range from 230 to 272 K. We develop a comprehensive description of the gas permeation based on the diffusion along the network of polyhedral cages, some of them being empty. Following earlier molecular dynamics simulation results, the jump from a cage to one of its empty neighbors is assumed to proceed via a “hole-in-cage-wall” mechanism involving water vacancies in cage walls. The rate-limiting process in the investigated temperature range can be explained by the creation of water-vacancy-interstitial pairs. The gas diffusion leads to a time-dependent cage filling which decreases across the hydrate layer with the distance from the particle surface. The model allows a prediction of the time needed for a complete conversion of ice spheres into clathrate as well as the time needed for a full equilibration of the cage fillings. The findings essentially support our earlier results obtained in the framework of a purely phenomenological permeation model in terms of the overall transformation kinetics, yet it provides for the first time insight into the cage equilibration processes. The diffusion of CO2 molecules through bulk hydrate is found to be about three to four times faster in comparison with the CH4 case.
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  • 90
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    American Chemical Society
    In:  In: Physical Methods in Food Analysis. American Chemical Society, Washington, DC, pp. 105-125. ISBN 9780841228856
    Publication Date: 2016-08-30
    Description: Consumer preference for natural food ingredients has increased in recent decades, and the natural food colorant market has grown to over one billion dollars annually. A variety of red, orange, and yellow natural colorants are approved and in use, but there still exists a lack of available blue and purple natural colorant options. The occurrence of blue colored compounds in the natural world is relatively rare. The isolation, identification, and characterization of natural blue and purple pigments obtained from underexplored natural sources such as from obscure terrestrial organisms and marine microorganisms will be discussed.
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  • 91
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    American Chemical Society
    In:  Analytical Chemistry, 83 (16). pp. 6395-6400.
    Publication Date: 2016-04-25
    Description: Titanium (Ti) is present as a trace element in seawater at extremely low concentrations (5-350 pM, where 1 pM = 10(-12) mol L(-1)) throughout the water column. Presently, little is known about the marine biogeochemistry of Ti and there is a distinct lack of oceanic measurements of Ti, because of the combined difficulties of trace-metal clean sampling for an element at such low levels and the lack of a suitable shipboard method of analysis. Here, a new cathodic stripping voltammetry procedure is presented for the rapid determination of Ti at pM concentrations in seawater that is capable of being used directly at sea. This method utilizes the catalytic enhancement of the reduction of the complex formed between Cupferron (N-nitrosophenylhydroxylamine) and Ti(IV). While Cupferron itself acts as both a complexing agent and an oxidizing agent, it was found that the optimal sensitivity was with bromate as an auxiliary oxidant. An advantage of this method is that it is useable over the pH range of 5.5-8. Under the conditions employed in this work, detection limits ranged from 5 pM to 12 pM. This new catalytic method is significantly more sensitive than existing methods and has been extensively tested at sea in the Atlantic and Southern Oceans.
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  • 92
    Publication Date: 2016-09-16
    Description: Electrolytes can thermodynamically inhibit clathrate hydrate formation by lowering the activity of water in the surrounding liquid phase, causing the hydrates to form at lower temperatures and higher pressures compared to their formation in pure water. However, it has been reported that some thermodynamic hydrate inhibitors (THIs), when doped at low concentrations, could enhance the rate of gas hydrate formation. We here report a systematic study of model natural gas (a mixture of 90% methane and 10% propane) hydrate formation in strong monovalent salt solutions in a broad range of concentrations, using a high pressure automated lag time apparatus (HP-ALTA). HP-ALTA can apply a large number (〉100) of cooling ramps to a sample and construct probability distributions of gas hydrate formation for each sample. The probabilistic interpretation of data enables us to mitigate the stochastic variation inherent in the nucleation probability distributions and facilitates meaningful comparison among different samples. The electrolytes used in this work are lithium chloride (LiCl), lithium bromide (LiBr), lithium iodide (LiI), sodium chloride (NaCl), sodium bromide (NaBr), sodium iodide (NaI), potassium chloride (KCl), potassium bromide (KBr), and potassium iodide (KI). We found that (1) some salts may act as kinetic hydrate promoters at low concentrations; (2) the width of the probability distributions (stochasticity) of natural gas hydrate formation in these salt solutions was significantly narrower than that in pure water. To gain further insight, we extended the study of the solutions of the same nine salts to the formation of ice and model tetrahydrofuran (THF) hydrate for comparison.
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  • 93
    Publication Date: 2020-05-11
    Description: Two new natural products, 3 and 4, and their predecessor 7-isocyanoisoneoamphilecta-1(14),15-diene (2), of the rare isoneoamphilectane class of marine diterpenes, along with the known amphilectane diterpenes 6–8, were isolated from the n-hexane extract of the marine sponge Svenzea flava collected at Great Inagua Island, Bahamas. The molecular structures of compounds 3 and 4 were established by spectroscopic (1D/2D NMR, IR, UV, HRMS) methods and confirmed by a series of chemical correlation studies. In a first ever case study of the assignment of the absolute configuration of a molecule based on the isoneoamphilectane carbon skeleton, the absolute configuration of compound 5 was established as 3S,4R,7S,8S,11R,12S,13R by application of vibrational circular dichroism (VCD). In vitro anti-TB screenings revealed that metabolites 2–4 and, in particular, semisynthetic analogue 5, are strong growth inhibitors of Mycobacterium tuberculosis H37Rv.
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  • 94
    Publication Date: 2020-05-11
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  • 95
    Publication Date: 2019-09-23
    Description: This paper proposes improved guidelines for dissolved organic matter (DOM) isolation by solid phase extraction (SPE) with a styrene-divinylbenzene copolymer (PPL) sorbent, which has become an established method for the isolation of DOM from natural waters, because of its ease of application and appreciable carbon recovery. Suwannee River water was selected to systematically study the effects of critical SPE variables such as loading mass, concentration, flow rate, and up-scaling on the extraction selectivity of the PPL sorbent. High-field Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS) and proton nuclear magnetic resonance (H-1 NMR) spectroscopy were performed to interpret the DOM chemical space of eluates, as well as permeates and-wash liquids with molecular resolution. Up to 89% dissolved organic carbon (DOC) recovery was obtained with a DOC/PPL mass ratio of 1:800 at a DOC concentration of 20 mg/L. With the 0 application of larger loading volumes, low proportions of highly oxygenated compounds were retained on the PPL sorbent. The effects of the flow rate on the extraction selectivity of the sorbent were marginal. Up-scaling had a limited effect on the extraction selectivity with the exception of increased self-esterification with a methanol solvent, resulting in methyl ester groups. Furthermore, the SPE/PPL extract exhibited highly authentic characteristics in comparison with original water and reverse osmosis samples. These findings will be useful for reproducibly isolating DOM with representative molecular compositions from various sources and concentrations and minimizing potential inconsistencies among interlaboratory comparative studies.
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  • 96
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    American Chemical Society
    In:  Journal of Proteome Research, 6 (2). pp. 540-545.
    Publication Date: 2020-07-20
    Description: Metabolomics offers great potential for understanding the metabolic consequences of exposure to chemicals and other stressors in the environment. Biological systems encompass humans exposed to chemicals in the environment as well as the diverse organisms inhabiting an ecosystem and exposed to environmental contaminants. An overall goal of environmental metabolomics is to understand what is metabolomically “normal” or adaptive and what constitutes a threat to human health and the environment.
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  • 97
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    American Chemical Society
    In:  Energy & Fuels, 12 (2). pp. 191-196.
    Publication Date: 2020-07-31
    Description: An overview is provided of time-independent physical/chemical properties as related to crystal structures. The following two points are illustrated in this review:  (1) Physical and chemical properties of structure I (sI) and structure II (sII) hydrates are well-defined; measurements have begun on sH. Properties of sI and sII are determined by the molecular structures, described by three heuristics:  (i) Mechanical properties approximate those of ice, perhaps because hydrates are 85 mol % water. Yet each volume of hydrate may contain as much as 180 volumes (STP) of the hydrate-forming species. (ii) Phase equilibrium is set by the size ratio of guest molecules within host cages, and three-phase (Lw−H−V) equilibrium pressure depends exponentially upon temperature. (iii) Heats of formation are set by the hydrogen-bonded crystals and are reasonably constant within a range of guest sizes. (2) Fundamental research challenges are (a) to routinely measure the hydrate phase (via diffraction, NMR, Raman, etc.), and (b) to formulate an acceptable model for hydrate formation kinetics. The reader may wish to investigate details of this review further, via references contained in several recent monographs.
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  • 98
    Publication Date: 2020-07-20
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  • 99
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    American Chemical Society
    In:  Journal of the American Chemical Society, 133 (15). pp. 5913-5920.
    Publication Date: 2020-07-16
    Description: The conversion of alkylboranes to the corresponding alkanes is classically per-formed via protonolysis of alkylboranes. This simple reaction requires the use of severe reaction conditions, that is, treatment with a carboxylic acid at high temperature (〉150 °C). We report here a mild radical procedure for the transformation of organoboranes to alkanes. 4-tert-Butylcatechol, a well-established radical inhibitor and antioxidant, is acting as a source of hydrogen atoms. An efficient chain reaction is observed due to the exceptional reactivity of phenoxyl radicals toward alkylboranes. The reaction has been applied to a wide range of organoboron derivatives such as B-alkylcatecholboranes, trialkylboranes, pinacolboronates, and alkylboronic acids. Furthermore, the so far elusive rate constants for the hydrogen transfer between secondary alkyl radical and catechol derivatives have been experimentally determined. Interestingly, they are less than 1 order of magnitude slower than that of tin hydride at 80 °C, making catechols particularly attractive for a wide range of transformations involving C−C bond formation.
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  • 100
    Publication Date: 2020-07-21
    Description: Chemicals targeting the liver stage (LS) of the malaria parasite are useful for causal prophylaxis of malaria. In this study, four lichen metabolites, evernic acid (1); vulpic acid (2), psoromic acid (3), and, (+)-usnic acid (4), were evaluated against LS parasites of Plasmodium berghei. Inhibition Of P. falciparum blood Stage (BS) parasites was also assessed to determine stage specificity. Compound 4 displayed the highest LS activity and stage specificity (LS IC50 value 2.3 mu M, BS IC50 value 47.3 mu M). The compounds 1 - 3 inhibited one Or more enzymes (Pf FabI, PfFabG, and pfFabZ), from the Plasmodial fatty acid biosynthesis (FAS-II) pathway, a potential drug. target for LS activity. To determine species specificity and to clarify the mechanism of reported antibacterial effects, 1-4 were also evaluated against FabI homologues and Whole cells of various pathogens -(S. aureus, E. coli M. tuberculosis). Molecular modeling studies suggest that lichen acids act indirectly via binding to allosteric sites on the protein surface of the FAS-II enzymes. Potential. toxicity, of compounds was assessed in human hepatocyte and cancer cells (in vitro) as well as in a zebrafish model (in vivo):. This study indicates the therapeutic and prophylactic potential of lichen metabolites as antibacterial and antiplasmodial agents.
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