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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 111-113 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ion [C3H5]+ generated in a chemical ionization source by a variety of methods, including protonation and charge exchange, exhibits a metastable peak for H2 loss which is two orders of magnitude weaker than that formed in an electron impact source. The stable [C3H5]+ ions generated by electron impact and chemical ionization undergo collision-induced dissociation to a comparable extent, both losing H2 by only one of the two competitive mechanisms observed for metastable ions. In contrast to the behavior of [C3H5]+, the molecular ions of p-substituted nitrobenzene, generated by charge exchange at high source pressure, yield composite metastable peaks for NO loss which are very similar in shape and intensity to those generated by electron impact. The contrasting behavior of the metastable ions extracted from high pressure ion sources in the two systems may be due to differences in the efficiencies of quenching of the ionic states responsible for fragmentation as metastable ions. It is noteworthy that the NO loss reactions require considerably lower activation energies than does the H2 loss reaction.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 585-596 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Infrared and X-ray diffraction studies have established that in the β-precipitation region of poly-L-glutamic acid the chains are in the β-conformation. Therefore, a major molecular conformational change has taken place upon precipitation. It is shown that the size of the α-helical aggregates remains constant with time in the β-region. Strong evidence can be offered to indicate that the transformation involves a transitory random-coil intermediate. Reasons are advanced, in view of the stability of the β-form, as to why two distinct precipitation regions exist.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 49-56 
    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: Blends of zinc neutralized sulfonated ethylene-propylene-diene elastomer (ZnS-EPDM) with poly(styrene-co-vinyl pyridine) have been compared with mixtures of the unfunctionalized rubber with the same copolymer. These binary component blends contain relatively low levels of interacting groups, which are, however, sufficient for the formation of intermolecular complexes. As a result of these interactions, marked enhancement in properties have been observed. In this study, small angle neutron scattering (SANS) is used to determine domain dimensions. The SANS experiments clearly show a decrease in domain size by three orders of magnitude when compatibilization via the sulfonate groups takes place. This reduction correlates with large changes in mechanical properties.
    Additional Material: 12 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 1-9 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Dissolution of sulfur-cured, carbon black-loaded copolymers and their blends with cis-1,4-polybutadiene (PBD) are brought about by boiling with o-dichlorobenzene which contains a small amount of 2,2′-dibenzamidodiphenyl disulfide. The resulting slurries are subjected to a sequence of separations which include high-speed centrifugation to remove solids, and solvent precipitation followed by filtration to isolate the precipitates. The precipitates are washed with solvent to remove soluble organic materials followed by carbon disulfide washing to dissolve the polymers. Cast films of the polymers are obtained by evaporating the carbon disulfide washings onto sodium chloride discs. The infrared spectra of the cast films of these preparations are very similar to those of their respective polymers prior to loading and curing. Calculations for relative concentrations of bound styrene and PBD microstructures permit nominal identification of the kinds of styrene-butadiene rubber and the amounts of cis-1,4-PBD used in a cured rubber formulation. Absorption bands used are near 3.35 μ for cis-1,4-PBD, 6.65μ for bound styrene, 10.35 μ for trans-1,4-PBD; and 11.0 μ for vinyl-1,2-PBD. Efforts are being made to improve the data by using a grafting infrared instrument and also to extend the calibrations to include other rubber blends.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 1171-1184 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal degradation of poly(methyl methacrylate) has been studied with unfractionated and fractionated polymer samples over a temperature range of 275-400°C. in a closed system by a new technique. Kinetic data have been obtained at temperatures about 100°C. higher than was possible previously. The results are compared with those obtained in open systems. Two main degradation reactions are operative. It is shown that the energies of activation for these reactions do not vary with polymer chain length in accordance with what is to be expected from the usually assumed depolymerization mechanisms. The termination reactions are diffusion-controlled. Hydrogenation by Adam's catalyst and bromination of the polymers have only moderate effects on the rate of degradation.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3241-3250 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reaction between styrene and n-butyllithium in benzene has been studied by spectrophotometry and calorimetry at 25°C. It was observed that the initiation of polymerization was first-order in styrene and one-third-order in butyllithium at styrene concentrations of 0.5 mole/l.. and that addition of butyllithium to styrene solutions caused an evolution of 1.7 kcal./mole of butyllithium. It was also noted that the rate of initiation was approximately an order of magnitude larger than that previously reported in very dilute styrene solutions (0.03 mole/l.) and comparable butyllithium concentrations. It is concluded that styrene stabilizes trimeric butyllithium relative to its hexamer by a nonstoichiometric, exothermic solvation process.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 14 (1983), S. 342-346 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectra of KClO3 are reported at room temperature up to pressures of 60 kbar in a diamond-anvil cell. The phase transition between phases I and II occurs at approximately 7 kbar, is sluggish and the spectra show that the two phases coexist over a pressure range of approximately 5 kbar. The Raman spectra of phases I and II differ appreciably in the Cl—O stretching region and the spectra of KClO3 II can be interpreted in terms of the predicted unimolecular rhombohedral cell which has no inversion centre. Mode Grüneisen parameters have been calculated for most of the modes observed and are used in an attempt to assign some of the lattice vibrations.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 21 (1990), S. 423-428 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lattice vibrations and internal modes of polycrystalline CH2ClI and CD2ClI have been studied as a function of temperature using Raman and far-infrared spectroscopy. Both isotopic forms have four phases; one is plastic, one is partially ordered and the other two are fully ordered. Some aspects of the structures are discussed.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 9 (1971), S. 49-53 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 427-431 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: HCO radical at a concentration of about 1014 cm-3 is produced by monochromatic laser photolysis of H2CO with a 0.6 mJ frequency-doubled, flashlamp-pumped dye laser pulse. Intracavity dye laser spectroscopy quantitatively monitors HCO absorbance near 614 nm as a function of delay time between photolysis and probing pulses. Rate constants for HCO + O2 and HCO + NO are found to be 4.0 ± 0.8 × 10-12 and 1.45 ± 0.2 × 10-11 cm3 molecule-1 sec-1.
    Additional Material: 2 Ill.
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