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  • Analytical Chemistry and Spectroscopy  (210)
  • Lunar and Planetary Science and Exploration  (98)
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  • 1
    Publication Date: 2019-07-17
    Description: Nanocrystal nonvolatile floating-gate memories are a good candidate for space applications - initial results suggest they are fast, more reliable and consume less power than conventional floating gate memories. In the nanocrystal based NVM device, charge is not stored on a continuous polysilicon layer (so-called floating gate), but instead on a layer of discrete nanocrystals. Charge injection and storage in dense arrays of silicon nanocrystals in SiO2 is a critical aspect of the performance of potential nanocrystal flash memory structures. The ultimate goal for this class of devices is few- or single-electron storage in a small number of nanocrystal elements. In addition, the nanocrystal layer fabrication technique should be simple, 8-inch wafer compatible and well controlled in program/erase threshold voltage swing was seen during 100,000 program and erase cycles. Additional near-term goals for this project include extensive testing for radiation hardness and the development of artificial layered tunnel barrier heterostructures which have the potential for large speed enhancements for read/write of nanocrystal memory elements, compared with conventional flash devices. Additional information is contained in the original extended abstract.
    Keywords: Lunar and Planetary Science and Exploration
    Type: Forum on Innovative Approaches to Outer Planetary Exploration 2001-2020; 4; LPI-Contrib-1084
    Format: text
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 396-402 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rotational barriers and 15N chemical shifts have been measured in a number of ureas and thioureas. As anticipated on the basis of the 15N shifts, several previously unobserved rotational barriers could be detected by using lanthanide reagents or a high field spectrometer. Nearly constant effects on both the rotational activation energy and the 15N shift are produced on going from ureas to the corresponding thioureas, and correlations are found between the ΔG
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 13 (1990), S. 170-172 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; Gas chromatography ; LC/GC ; On-line coupling ; Metal complexes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The on-line coupled LC-GC technique was applied to the analysis of several metal chelates of N,N-diethyldithiocarbamic acid. A 10-port valve interface was used to couple the LC and GC instruments. Conditions during sample transfer into the GC gave fully concurrent solvent evaporation. The chelates investigated were separated with a short apolar fused silica column. LC preseparation was made with cyano or amino phases using a hexane/dichloromethane mixture as eluent. On-line LC-GC combination seems to be very suitable for the separation of the metal chelates studied.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2019-07-13
    Description: Spherules of glass varying in size from a few micrometres to a few millimetres are common in the lunar regolith. While some of these glass beads are products of pyroclastic fire fountains others originate as impact melt ejected from the target that breaks into small droplets and solidifies as spherical particles while raining back to the lunar surface. These glasses preserve information about the chemical composition of the target and often contain sufficient amount of radioactive nuclides such as 40K to enable Ar-40-Ar-39 dating of individual beads. Studies measuring the age of glass beads have been used in attempts to establish variations in the flux of impactors hitting the Moon, particularly during the period that postdates the formation of major impact basins [1,2]. These studies proposed a possibility of spike in the impact flux about 800 Ma [2] and over the last 400 Ma [1]. More recently U-Th-Pb isotopic systems have been also utilized to determine the age of impact glasses from the Apollo 17 regolith [3]. Our aim is to extend the application of the U-Pb system in impact glasses to spherules isolated from Apollo 14 soil 14163 in an attempt to further investigate the applicability of this isotopic system to the chronology of impact glass beads and gain additional information on the impact flux in the inner Solar system.
    Keywords: Lunar and Planetary Science and Exploration
    Type: JSC-CN-27960 , Lunar and Planetary Science Conference; Mar 18, 2013 - Mar 22, 2013; The Woodlands, TX; United States
    Format: application/pdf
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 3 (1989), S. 217-221 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Sequential daughter-ion-scanning analyses of small peptides have been performed using a hybrid tandem instrument of BEqQ configuration. Precursor ions are selected by B and allowed or induced (by high-energy collisional activation) to decompose in the region preceding E. Decoupling of E from the accelerating voltage permits the selection of the first-generation daughter ion whilst retaining appropriate float voltages for the quadrupole assemblies. The daughter ion selected by E is further subjected to low-energy collisional-activation dissociation (CAD) in q and the fragment-ion spectrum is obtained by scanning Q. The sequential daughter-ion-scanning technique has been used to establish that ‘internal’ fragments of the types, (AY′) and (BY′), are formed via initial Y-type cleavage. Fragmentation of a protonated peptide (angiotensin III) by loss of the C-terminal amino acid residue, yielding a (Bn′ + OH) ion, is reported for the first time. This process is analogous to that previously described for metal-cationized peptides.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 13-15 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The characteristics of the detection of ions of the alkali metals and of cluster ions of the type (H2O)NMH+ (where M is an amino acid) are markedly different from those for the detection of protonated saccharose ions. The latter are shown to produce a signal from a secondary electron multiplier detector at a lower ion energy than the threshold energy for the former ions. An explanation is proposed in terms of the charge localization.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 125-128 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Double-electron-capture reactions in which singly charged projectile ions A+ convert to negative ions A- in collisions with molecules M are endoergic. Non-zero cross-sections for the reactions occur when the endoergicities fall within a ‘reaction window’. The existence of a window for reactions with CH3Br molecules is demonstrated in this investigation by altering the population of ground and excited states of the resulting CH3Br2+ ions using three projectile ions, S+·, OH+ and F+ which markedly alters the endoergicities of the double-electron-capture reactions. Analysis of the energy-loss spectra indicates that the reaction window for CH3Br is between endoergicities of about 8 and 22 eV. Using F+ as the projectile ion, it is shown that the population of the more highly excited states of CH3Br2+ is enhanced.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 2 (1988), S. 167-169 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Two methods of calibrating the energy-loss scale in charge-stripping experiments are compared. It is shown that the linear-offset method rather than the multiplicative method should be used.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 9-12 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Discrimination effects in secondary electron multipliers due to the differences in kinetic energy with which ions of different masses strike the dynode surface are investigated. The threshold energy at which ions of a particular mass can be detected is discussed. The efficiencies of such multipliers when used with cluster ions such as H+(H2O)N (where Cat+ represents an alkali-metal cation) are investigated and discussed, in terms of both the ‘kinetic’ and ‘potential’ emission coefficients.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 438-448 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: High-resolution double-charge-transfer spectroscopy has been used to measure the double-electron-capture reactions with CH4. Using kilo electron volt OH+, CI+ and F+ projectile ions it is possible in double-electron-capture reactions with CH4 molecules to populate the ground triplet state of CH42+. The energy of this state relative to the gound state of CH4 is found to be 38.2±0.4 eV, while the fiest excited triplet state is found at a double-ionization energy of 46.7±0.8 eV. In double-electron-capture reactions involving H+ projectile ions and CK4 molecules, low-lying singlet states of CH42+ are populated. The energies of the four lowest singlet states in CH42+ were measured to be 39.2±0.4, 40.5±0.4, 42.1±1 and 51.0±1 eV. High-resolution photon-induced Auger-electron spectra of the CH4 molecule have been recorded. The KLL Auger Spectrum shows four distinct structures in the 30-70 eV double-ionization evergy range centred at 40.3±0.1, 47.03, 53.2±0.3 and 6.9±0.3 eV. The previously published data on CH42+ have been reviewed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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