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  • Analytical Chemistry and Spectroscopy  (25,033)
  • LUNAR AND PLANETARY EXPLORATION  (14,409)
  • SPACE SCIENCES  (12,837)
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Keywords
Publisher
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  • 1
    Electronic Resource
    Electronic Resource
    Vibrational dephasing of the ν3 mode of liquid allene (1986)
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 17 (1986), S. 477-480 
    Details
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectrum of the ν3 mode of allene has been studied as a function of temperature throughout the temperature range of the liquid. Analysis of the spectral band shape shows that the vibrational dephasing is a fast-modulation process. Evidence is presented for a vibrational-rotational coupling involving the tumbling reorientation of the molecule. Dilution studies in GeH4 indicated significant resonant vibrational energy transfer.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jrs.1250170610
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  • 2
    Electronic Resource
    Electronic Resource
    Determination of benzene alkyl derivatives in heavily loaded environmental aqueous samples by means of combination of distillation and purge and trap-gas chromatography-mass spectrometry (1997)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 20 (1997), S. 482-486 
    Details
    ISSN: 0935-6304
    Keywords: Volatile benzene alkyl derivatives ; Simple distillation ; Purge and trap ; Capillary gas chromatograph-mass spectrometry ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Simple distillation was used to prepare aqueous environmental samples (especially those with high content of accompanying dissolved and suspended organic and inorganic matter) for determination of benzene, toluene, ethylbenzene, and xylenes (BTEX) by means of purge and trap (PT) coupled to gas chromatography-mass spectrometry (GC-MS). The PT step was carried out with a laboratory-built device in which alalytes desorbed from a Primary trap (macrotrap) are focused in a microtrap (also with sorbent) and moisture is removed from purge gases by a Nafion tube (walls selectively permeable to water vapor). Recoveries, if only the first 10 ml distillate was collected, were of the order of 40% at optimum distillation parameters. At a probability level of 95% recoveries were independent of concentration in a studied concentration range of 0.50-30 ppb. Enrichment factors for distillation were of the order off 20. Real samples, i.e., raw and treated waste water were analyzedc for BTEX content by the developed medthod.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240200904
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  • 3
    Electronic Resource
    Electronic Resource
    An energy-resolved study of the fragmentation of ionized 1-Penten-3-ol (1984)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1984), S. 573-576 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed energy-resolved study of the fragmentation of CH2=CHCH(OH)CD2CD3 (1-d5) has been carried out using metastable ion studies and charge exchange techniques, combined with collision-induced dissociation studies to establish the structures of fragment ions. At low internal energies (metastable ions) the molecular ion of 1-d5 rearranges to the 3-pentanone structure and fragments by loss of C2H5 or C2D5 leading to the acyl structure, [CH3CH2C≡O]+ or [CD3CD2C≡O]+, for the fragment ion. However, with increasing internal energy of the molecular ion this rearrangement process decreases rapidly in importance and loss of C2D5 by direct cleavage, leading to [CH2=CHCH=OH]+, becomes the dominant fragmentation reaction. As a result the [C3H5O]+ ion seen in the electron impact mass spectrum of 1-penten-3-ol has predominantly the protonated acrolein structure.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210191109
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  • 4
    Electronic Resource
    Electronic Resource
    Negative ion field desorption mass spectrometry by clustering with anions (1981)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1981), S. 312-315 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that under field desorption conditions some less volatile or non-volatile compounds such as oligosaccharides, sulphonic acids and fatty acids can be ionized below the threshold of field electron emission by clustering with anions. In all cases the sample, together with polyethylene oxide 4000, is dissolved in water. The source of the clustering anion is provided either by a small amount of a salt added to this solution (sugars) or by the compounds themselves (sulphonic and fatty acids). The solution is applied to unactivated and/or slightly activated 10 μm tungsten wire cathodes. Suitable clustering ions for the sugars appear to be [Cl]-, [NO3]- and to a lesser extent [Br]- and [I]-. Most of the sulphonic acids studied give rise to the formation of [Mn - H]- ions (n≤5), but their potassium salts yield only unclustered sulphonate anions. However, the addition of a small amount of LiCl to the mixture of benzene sulphonic acid and polyethylene oxide 4000 promotes the formation of clustered anions, [(M - H)2Li]- being by far the most abundant if activated cathodes are used. This addition of some LiCl is essential in the case of fatty acids: without LiCl no anions may be desorbed at all from activated wires, but with the presence of LiCl both [M - H]- and the most abundant [(M - H)2Li]- anions are easily generated.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200080706
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  • 5
    Electronic Resource
    Electronic Resource
    A 15N labelling, FD and FAB study of ammonia loss from protonated arginine molecules (1983)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1983), S. 525-529 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The positive ion field desorption (FD) spectrum of arginine taken at the best anode temperature only contains a peak due to [M+H]+ ions. At higher emitter temperatures a considerable amount of fragmentation is induced and the [M+H—NH3]+ ions become most abundant. Specific 15N labelling reveals that the eliminated ammonia molecule, exclusively, contains one of the terminal nitrogen atoms of the guanidyl group. This also applies to the ammonia loss from metastably decomposing [M+H]+ ions. The positive ion fast atom bombardment (FAB) spectrum shows more fragmentation than the FD spectrum. In contrast with the FD results, the [M+H]+ ions generated upon FAB with ion lifetimes 〈10-6 s eliminate both ammonia containing one of the terminal nitrogen atoms of the guanidyl group and ammonia containing the α-amino group in the ratio of 1.35, as found by 15N labelling. The metastably decomposing [M+H]+ ions, however, eliminate only the former ammonia molecule. In the negative ion FD and FAB spectra no other peak than that corresponding to the [M—H]- ion is observed. Some attention has been paid to the thermal degradation of arginine on the basis of a few Curie-point pyrolysis experiments.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210181206
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  • 6
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    Direct detection of C4H2 photochemical products - Possible routes to complex hydrocarbons in planetary atmospheres (1992)
    In:  Other Sources
    Details
    Publication Date: 2019-08-28
    Description: The photochemistry of diacetylene (C4H2), the largest hydrocarbon to be unambiguously identified in planetary atmospheres, is of considerable importance to understanding the mechanisms by which complex molecules are formed in the solar system. In this work, the primary products of C4H2's ultraviolet photochemistry were determined in a two-laser pump-probe scheme in which the products of C4H2 photoexcitation are detected by vacuum ultraviolet photoionization in a time-of-flight mass spectrometer. Three larger hydrocarbon primary products were observed with good yield in the C4H2 + C4H2 reaction: C6H2, C8H2, and C8H3. Neither C6H2 or C8H3 is anticipated by current photochemical models of the atmospheres of Titan, Uranus, Neptune, Pluto, and Triton. The free hydrogen atoms that are released during the formation of the C8H3 and C8H2 products also may partially offset the role of C4H2 in catalyzing the recombination of free hydrogen atoms in the planetary atmospheres.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Science (ISSN 0036-8075); 258; 5088; p. 1630-1633.
    Format: text
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  • 7
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    Infrared emission during simulated lunar eclipse. (1967)
    In:  Other Sources
    Details
    Publication Date: 2019-07-13
    Description: IR emission measurement of lunar-like materials during simulated eclipse, noting dependence on time
    Keywords: SPACE SCIENCES
    Type: AIAA PAPER 67-290 , ; - QUANTUM ELECTRONIC|THERMOPHYSICS SPECIALIST CONFERENCE; Apr 17, 1967 - Apr 20, 1967; NEW ORLEANS, LA
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  • 8
    Electronic Resource
    Electronic Resource
    Biodegradation of Pharmaceutical Residues Investigated by SPE-GC/ITD-MS and On-Line Derivatization (2000)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 474-478 
    Details
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Solid-phase extraction, on-line derivatization, and measurement by ion trap mass spectrometry (ITD-MS) were used to investigate the biological degradation of pharmaceutical residues (clofibric acid, ibuprofen, diclofenac). The results of the single steps of sample pretreatment and analytical determination are reported. MS/MS measurements were performed on an ITD-MS by selecting collision induced dissociation of the molecular ions (M+) as parent ions to defined daughter ions. A pilot sewage plant and biofilm reactors operating under oxic and anoxic conditions were run as model systems with synthetic sewage water containing 10 to 50 mg/L dissolved organic carbon (DOC) and pharmaceuticals in concentrations of 10 μg/L. Clofibric acid displayed its persistent character in all cases. The pilot sewage plant and the oxic biofilm reactor showed comparable results for diclofenac and ibuprofen, which both were partly degraded. These results can explain the occurrence of these substances in sewage effluents and in the aquatic environment. A high degree of degradation was found especially for ibuprofen in the oxic biofilm reactor, which was attributed to adaptation of the biofilm to the residue. Two metabolites of ibuprofen could be identified on the basis of their mass spectra and comparison with literature data, viz. hydroxyibuprofen and carboxyibuprofen.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
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    Interaction of the plasma tail of comet Bradfield 1979L on 1980 February 6 with a possibly flare-generated solar-wind disturbance (1983)
    In:  CASI
    Details
    Publication Date: 2019-06-28
    Description: Solar-wind plasma data from the ISEE-3 and Helios 2 spacecraft were examined in order to explain a uniquely rapid 10 deg turning of the plasma tail of comet Bradfield 1979l on 1980 February 6. An earlier study conducted before the availability of in situ solar-wind data (Brandt et al., 1980) suggested that the tail position angle change occurred in response to a solar-wind velocity shear across the polar component changed by approximately 50 km/s. The present contribution confirms this result and further suggests that the comet-tail activity was caused by non-corotating, disturbed plasma flows probably associated with an Importance 1B solar flare.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: NASA-TM-85617 , NAS 1.15:85617 , DE83-011332 , LA-UR-83-1023 , CONF-821159-6 , Solar Wind 5 proceedings
    Format: application/pdf
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  • 10
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    Ions of Jovian origin observed by Voyager 1 and 2 in interplanetary space (1980)
    In:  Other Sources
    Details
    Publication Date: 2019-06-27
    Description: Burst-like and long-lived ion fluxes (E greater than 30 keV) of Jovian origin have been observed in interplanetary space by the LECP instrument on the Voyager 1 and 2 spacecraft. Burst (few minute duration) events are observed at distances greater than 0.6 AU from Jupiter. These events are highly anisotropic and possess steep energy spectra, while long-lived (greater than 8 hour duration) events have relatively steady fluxes at low energies, strong anisotropies that decay with time, and a variable high energy component. Both types of events usually display simultaneous onsets and sharp cutoffs for all energies, an excess of atomic number Z not less than 6 particles compared to solar and interplanetary events, and particle flow directions pointed away from Jupiter along the local interplanetary magnetic field. The origin for the long-lived events appears to be inside the bow shock of the planet.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Geophysical Research Letters; 7; June 198
    Format: text
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