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  • Chemistry  (87)
  • STRUCTURAL MECHANICS
  • Geophysics
  • 1985-1989  (47)
  • 1980-1984  (42)
  • 1
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using fast atom bombardment (FAB) ionization combined with tandem mass spectrometry (MS/MS), the identity of arsenobetaine (AB) in extracts of sole, haddock, lobster and shrimp was unequivocally confirmed. Evidence was also presented for the presence of arsenocholine (AC) in the shrimp extract. Confirmation was obtained by comparing the collision-induced dissociation (CID) daughter ion and parent ion spectra of major ions in the FAB spectra from these extracts with those from the authentic standards.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 25 (1987), S. 359-360 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 25 (1987), S. 267-267 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 15 (1988), S. 615-621 
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The collisionally activated decomposition of [M + H]+ ions, generated by fast atom bombardment (FAB) of glutathione conjugates, has been studied by tandem mass spectrometry (MS/MS) using hybrid sector/quadrupole instruments. Abundant fragments of diagnostic utility were present in the daughter ion spectra. Common fragmentation modes were observed but their relative importance was strongly dependent on the nature of the conjugated species. As an example of a general approach to the characterization of glutathione conjugates in biological samples, the acetaminophen-glutathione conjugate was identified in rat bile, following coadministration of (2H0)- and (2H3)acetaminophen, using the experimental sequence: (i) conventional FAB mass spectrometric analysis, (ii) MS/MS using constant neutral loss (129 u) scanning to identify parent ions corresponding to glutathione conjugates, (iii) MS/MS to yield daughter ion spectra of parents so identified and corresponding to (2H0)- and (2H3)-labeled conjugates.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 477-478 
    ISSN: 0935-6304
    Keywords: Capillary SFC ; Reproducibility ; Pump filling method ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 6
    ISSN: 0935-6304
    Keywords: Gas chromatography, GC ; Fused silica capillary columns ; Retention index ; Internal standards ; Environmental samples ; Dichlorobenzyl alkyl ethers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A homologous series of 2,4-dichlorobenzyl alkyl ethers (DCBEs) have been synthesized and purified for use as retention index calibrants and internal standards. They are stable, sensitive to ECD and FID and ideal for GC-MS, with base peaks at m/z 159/161. The retention index calibration against the n-alkanes for a linear temperature program (LTP) series is given and recommendations made for the most suitable members of the DCBE series for use as internal standards in organochlorine (OC) residue analysis.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1985), S. 139-141 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Analysis for oestradiol bis-tert-butyldimethylsilyl ether by gas chromatography/mass spectrometry (GC/MS) with selected reaction monitoring ([M]+. → [M-C4H9]+) using a tandem double-focusing/quadrupole instrument gave a detection limit below 10 pg. During analyses of a plasma extract, the selectivity of detection was superior to conventional selected ion monitoring. A parent ion resolution of 5000 was used to eliminate detection of all components but the chosen analyte.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 1109-1116 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The solvent has an influence on the homogeneity of the poly(vinyl methyl ether)-polystyrene, PVME-PS blends Prepared by drying cosolutions. This influence has been analyzed in terms of the competition among polymer-polymer and polymer-solvent interactions. Model solutions have been prepared in which intermoleeular interactions correspond to the interactions in this blend and in some of the cosolutions. These interactions in the model solutions have been detected and identified by applying Rummens' method. The 13C NMR spectra have been determined for PVME and for styrene oligomer dissolved in n-alkanes, cyclohexane, diethyl ether, isopropyl methyl ether, diisopropyl ether, and chloroform, and for PVME dissolved in benzene, toluene, and cumene. The chemical shifts have been plotted against the parameter g2 = [(n22 - 1)/(n22 + 1)]2, where n2 is the refractive index of the solvent. If the structural segment represented by certain carbon and some solvent has an interaction that is stronger than dispersive, the chemical shift for this carbon will deviate from the line formed by its shifts in n-alkane solutions, these deviations indicate characters and intensities of the intermoleeular interactions. Results indicate that cyclohexane exhibits weak interactions with both of the polymers and does not interfere with their mutual interaction, leading to a compatible blend. Results also suggest that benzene and toluene interact in the PVME in the same manner as PS. This leads to a gradual increase of the number of polymer-polymer interactions as the concentration of the polymers is increased by solvent removal, resulting in a compatible blend. Chloroform apparently interacts more strongly with PVME than with PS but interacts strongly enough with both to restrict interaction among the two polymers. As the concentration of polymers in the cosolution is increased, PS forms a separate phase. This leads to an inhomogeneous blend when the solvent is evaporated.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 433-439 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The deformation behavior of miscible amorphous/amorphous PMMA/PEO poly(methyl methacrylate)/poly(ethylene oxide) blends was compared with that of pure PMMA. Small-angle neutron scattering experiments were performed on labeled systems made of PEO + D-PMMA + HPMMA. Characteristic molecular parameters such as radius of gyration, Rg, molecular weight, Mw, and interaction parameter, X, were extracted from the coherent scattering cross sections, Molecular anisotropy was measured on the solid state coextruded samples, and the observed drawing efficiency is compared with, the results of shrinkage tests. In the case of PMMA/PEO blends, anomalous scattering behavior precludes any quantitative Interpretation of the scattering patterns, but revealed important structural changes upon drawing, namely a deformation-induced phase separation.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 393-395 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: High-density polyethylene of high tensile modulus has been produced by solid state extrusion using an Instron capillary rheometer. Microhardness measurements on these ultraoriented fibers have been made to assess their perfection from values of the tensile elastic modulus and shear strength. The microhardness tests were measured using a Vickers square diamond. The microhardness increased with the common temperature for crystallization and extrusion, likely due to improvement in the lateral packing of microfibrils. The variation of microhardness with draw ratio is also illustrated.
    Additional Material: 5 Ill.
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