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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 69 (1998), S. 1353-1358 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A negative ion sputter source incorporating a microbeam Cs+ source intended for application in accelerator mass spectrometry (AMS) has been developed from a General Ionex HICONEX 834™ source. (HICONEX is a trade mark of High Voltage Engineering Europa.) The source is part of a microbeam AMS system, designed for in situ microanalysis of geological samples known as AUSTRALIS (AMS for UltraSensitive TRAce eLement and Isotopic Studies) recently developed at the Heavy Ion Analytical Facility laboratory. With requirements of precise beam positioning on mineralogical samples, a high magnification sample viewing system is a vital part of the source, enabling live observation of the sputtering process and visual tuning of the primary beam. Microbeam of Cs+ of 30 μm in diameter can be produced routinely with adequate intensity for a number of applications. The "screen" electrode in the secondary ion extraction system facilitates steering of the primary beam affected by the extraction field, back into the geometric center of the sample. The injector system includes high resolution electric and magnetic analyzers, improving the background suppression before injection into the accelerator. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 69 (1998), S. 1075-1075 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A negative ion sputter source incorporating a microbeam Cs+ source intended for application in accelerator mass spectrometry (AMS) has been developed from a General Ionex HICONEX 834™ source. (HICONEX is a trade mark of High Voltage Engineering Europa.) The source is part of a microbeam AMS system, designed for in situ microanalysis of geological samples known as AUSTRALIS (AMS for UltraSensitive TRAce eLement and Isotopic Studies) recently developed at the Heavy Ion Analytical Facility laboratory. With requirements of precise beam positioning on mineralogical samples, a high magnification sample viewing system is a vital part of the source, enabling live observation of the sputtering process and visual tuning of the primary beam. Microbeam of Cs+ of 30 μm in diameter can be produced routinely with adequate intensity for a number of applications. The "screen" electrode in the secondary ion extraction system facilitates steering of the primary beam affected by the extraction field, back into the geometric center of the sample. The injector system includes high resolution electric and magnetic analyzers, improving the background suppression before injection into the accelerator. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 32 (1993), S. 403-408 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 32 (1993), S. 397-402 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 31 (1992), S. 1881-1889 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 385 (1982), S. 109-132 
    ISSN: 0375-9474
    Keywords: Nuclear reactions
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 7 (1990), S. 253-269 
    ISSN: 1572-879X
    Keywords: Fischer-Tropsch synthesis ; The Shell Middle Distillate Synthesis Process (SMDS) ; syngas chemistry ; natural gas conversion ; liquid hydrocarbons ; chain-length-independent FT chain-growth reaction ; chain-length-dependent cracking process ; combustion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Since the early 1970s Shell's research has been involved in syngas chemistry with special focus on routes to convert (remote) natural gas into easily transportable liquid hydrocarbons. This has resulted in the development of the SMDS process. The world's first commercial SMDS plant is being constructed on a site adjoining the Bintulu LNG plant in Sarawak, Malaysia, and will come on stream in the last quarter of 1992. The heart of SMDS is an enhanced Fischer-Tropsch process. However, direct FT synthesis does not allow the selective production of materials of narrow carbon number range. To overcome this limitation the flexible two-stage concept of SMDS has been developed, which combines the chain-length-independent FT chain-growth reaction with a chain-length-dependent cracking process. Naphtha, kerosene and gas oil yield ratios can be varied from 15∶25∶60 to 25∶50∶25. Both the kerosene and gas oil show excellent combustion properties: the smoke point of the kerosene can be over 45 mm and the gas oil has a cetane number in excess of 70. Further attention is paid to the production of the synthesis gas because of its impact on overall process efficiency, to the selection of multitubular FT reactors, and to the environmental merits of the SMDS process and its clean, aromatics-free products.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Crystalline primary inclusions in diamonds from the Argyle and Ellendale lamproites have been analyzed for Mn, Ni, Cu, Zn, Ga, Pb, Rb, Sr, Y, Zr, Nb, Ta, Ba and Mo by proton microprobe. Eclogite-suite inclusions dominate at Argyle and occur in equal proportions with peridotite-suite inclusions at Ellendale. Eclogitic phases present include garnet, omphacitic clinopyroxene, coesite, rutile, kyanite and sulfide. Eclogitic clinopyroxenes are commonly rich in K and contain 300–1060 ppm Sr and 3–70 ppm Zr: K/Rb increases with K content up to 1400 at 0.7–1.1% K. Rutiles have high Zr and Nb contents with Zr/Nb=1.5–4 and Nb/Ta ∼16. Of the peridotite-suite inclusions, olivine commonly contains 〉 10 ppm Sr and Mo; Cr-pyropes are depleted in Sr, Y and Zr, and enriched in Ni, relative to eclogitic garnets. Eclogite-suite diamonds grew in host rocks that were depleted in Mn, Ni and Cr, and enriched in Sr, Zn, Cu, Ga and Ti, relative to Type I eclogite xenoliths from the Roberts Victor Mine. Crystallization temperatures of the eclogite-suite diamonds, as determined by coexisting garnet and clinopyroxene from single diamonds, range from ∼1085 to ∼1575° C. Log K D (C i cpx /C i gnt ) varies linearly with 1/T for Zr, Sr and Ga in most of the same samples. This supports the validity of the temperature estimates; Argyle eclogite-suite diamonds have grown over a T range ≥400° C. Comparison with data from eclogite xenoliths in kimberlites suggests that K D Sr and K D Zr are mainly T-dependent, while K D Ga may be both temperature-and pressuredependent. K D Ni , K D Cu and K D Zn show no T dependence in these samples. In several cases, significant major-and/or trace-element disequilibrium is observed between different grains of the same mineral, or between pyroxene and garnet, within single diamonds. This implies that these diamonds grew in an open system; inclusions trapped at different stages of growth record changes in major and trace-element composition occurring in the host rock. Diamond growth may have been controlled by a fluid flux which introduced or liberated carbon and modified the composition of the rock. The wide range of equilibration temperatures and the range of composition recorded in the inclusions of single diamonds suggest that a significant time interval was involved in diamond growth.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Inst. and Methods in Physics Research, B 92 (1994), S. ix-x 
    ISSN: 0168-583X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 103 (1989), S. 199-202 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Proton microprobe analyses of the minerals in garnet-peridotite xenoliths from kimberlites show that the partitioning of Ni between chrome pyrope garnet and olivine is strongly temperature(T)-dependent. The range of Ni contents in olivines is small relative to that in the analyzed garnets; a geothermometer therefore can be derived, based only on the Ni content of garnet. This allows estimation of T for single Cr-pyrope grains, such as the inclusions in diamonds, if these can be assumed to have equilibrated with olivine.
    Type of Medium: Electronic Resource
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