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  • 1
    Publication Date: 1992-05-01
    Print ISSN: 0170-0839
    Electronic ISSN: 1436-2449
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 28 (1992), S. 319-325 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Alternating copolymers of α-methylstyrene (α-MeSt) with N-alkylmaleimides (RMI; R=Et, n-Pr, iso-Pr, n-Bu, n-Hex) were prepared in Calvet differential microcalorimeter under different monomer-to-monomer ratios in the feed using AIBN as initiator. The equilibrium constants of CT-complex monomers have low values: 0.02–0.05 L.mol-1 but the mechanism of copolymerization indicates the participation of CT-complex. Equilibrium constants and rate of decomposition under the TGA conditions are not dependent on steric factors, but the rate of copolymerization decreases with the increase of bulkiness of alkyl substituent. In high conversion copolymerization it was observed that in the presence of an excess of homopolymerizable RMI, alternating copolymers are quantitatively formed prior to the formation of poly(RMI).
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Composite materials consisting of natural leather and polyurethane elastomers, and bonded together by polyurethan adhesives, were submitted to accelerated ageing at various testing conditions.The extent of the degradation of these composites was evaluated through the determination of mechanical strength reduction and through the insight into the structural and chemical transformations of the adhesive polymeric materials.Founded data correlations indicate to the mechanism and to the relevant factors that influence of ageing processes.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rigid polyurethane, PUR, foam was prepared by reacting diphenylmethane diisocyanate, MDI, with aliphatic correactants of polyether type.The insulating pipe was made by moulding technic. The PUR pipe was subjected to isothermal aging by special equipment which was constructed for this purpose in order to study the structural changes in PUR foam under various temperatures and to define the maximal temperature at which it might be used as insulation in insulating pipes.The structural changes of PUR foam were studied by means of spectrophoto-metric measurement and thermal analysis.The evidence of thermal degradation of PUR foam has been found. Its course and intensity depend upon the temperature and differ throught the verticale cross-section of the insulating pipe.The correlation between chemical changes of PUR foam and its physical properties are also discussed.
    Additional Material: 7 Ill.
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  • 5
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The samples of vulcanized rubber compounds with natural rubber (NR) and styrene-butadiene rubber (SBR) were prepared. The surface chlorination of samples was performed by immersion of strips in aqueous solution of sodium hypochlorite and in hydrochloric acid in dependence of time and in temperature range from 20 °C to 80°C. The changes of chemical structures, thermal stability and morphological properties of chlorinated vulcanizates were recorded by IR-FMIR spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), wide angle X-ray diffraction (WAXD) and scanning electron microscopy (SEM). Extremely heterogeneous complex mechanisms of chlorination and parallel degradation processes in dependence on time and temperature above all were indicated and compared to NR and SBR vulcanizates. At higher temperatures the structural changes in elastomeric matrix in connection with selective separation and surface migration of multicomponent filler due to agressive media were observed.
    Additional Material: 6 Ill.
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  • 6
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Comparative investigations of the polymeric residues remained after degrading polystyrene by heat or by UV irradiation reveal numerous profound changes of the structural and molecular parameters of the polymer when subjecting it to either of these main types of degradation.The polymeric residues of the commercial and of the prepared polystyrene samples were investigated in view of the following characteristics: discolouration, IR, UV and 13C NMR spectra, DSC-analysis, GPC-elution curves and X-ray patterns.The results show pronounced heterogeneity of the degradative reactions occuring in the framework of the thermal and photochemical degradation of polystyrene, including the existence of crosslinking processes and producing thus very inhomogeneous polymeric material.The presumption of the existence of different mechanism paths occuring in various polystyrene structural fractions was confirmed and further promoted, especially from the standpoint that the lower-molecular fractions of the polymer should behave more sensitively against the degradative attacks.Many-sided meanings of the informations obtained by analysing degraded polystyrene samples allow to postulate the present degradative mechanism by comparing among them various types of de gradative processes.The gained informations about the locations and ranges of absorption bands in UV, IR and 13C NMR spectra, as well as the complementary evidence from other determinations enabled the claim that polystyrene thermo-oxidative degradation would preferentially take place in the way to produce acetophenone structures near the chain ends. In the initial degradation periods this would be related with substantial lowering of the molecular mass.The photo-oxidative degradation mechanisms cause the build-up ketone and aldehyde structures and ring-opening reactions concurrent with chain crosslinking reactions.Comparing long-wave and short-wave UV irradiations of polystyrene does not only show the existence of inequal induction times, but additionally the presence of two sets of similar reactions leading to the production of many oxidized structures.The investigations would show that oxidative polystyrene degradation is a very complex phenomenon in which the prefered courses of chemical reactions are in the relations to the initial reaction steps, namely they do depend on structures formed in the early stages of the thermal and photo-degradative processes.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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