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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 68 (1957), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8927
    Keywords: Optical spectroscopy ; bolaform electrolytes ; ion pairs ; ion-pair aggregation ; glyme-separated ion pairs ; α,ω-(9-fluorenylsodium)-polymethylenes ; fluorenylsodium ; tetraglyme ; tetrahydrofuran ; tetrahydropyran
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Formation constants of tetraglyme (glyme 5) separated ion pairs of bolaform electrolytes of the type Na+,−Fl(CH2) n Fl−, Na+ (Fl− denoting a fluorenyl carbanion) were measured spectrophotometrically in tetrahydrofuran (THF) and tetrahydropyran (THP) at 25°C as a function of the chain lengthn, withn=2, 3, 4, or 6. The ratiosK 1/K 2 of the first and second glyme ion-pair separation steps were found to be equal to the statistical factor 4 in all cases except in THP for the compoundn=2, where the ratio is 15. Values ofK 1 as well as K 2 increase considerably with chain length, the former by a factor 19 asn increases from 2 to 6. The ion-pair separation with glyme 5 is easier in THP than in THF. The results are discussed in terms of differences in external cation solvation and the possible involvement of cyclized structures or curled conformations as a result of interactions between the terminal ion pairs.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 1264-1269 
    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: Thermal properties of Fortron®®Registered trademark of Hoechst Celanese Corporation. poly(phenylene sulfide) (PPS) polymers of different molecular weights were studied by DSC. Crystallization studies revealed that the ability of these polymers to crystallize decreases with increasing molecular weight. The Avrami equation poorly describes the isothermal crystallization of PPS. Lamellar crystallization was observed for the lowest molecular weight sample. For the other, higher molecular weight polymers the Avrami exponent is always between 2 and 3, suggesting development of distorted spherulites with heterogeneous nucleation. The temperature dependence of the solid and melt heat capacities have been determined. The solid specific heat capacity did not exhibit a molecular weight dependence. The heat capacity increase at the glass transition, Tg, has been calculated to be 28.1 J°C-1 mole-1. The equilibrium melting point of PPS has been estimated to be 348.5°C using the Hoffman-Weeks method. The Tg of PPS increases with molecular weight. The Tg of the highest molecular weight evaluated is 92.5°C. A DMA relaxation peak corresponding to the onset of the phenylene ring rotation occurs at -92°C. Only the highest molecular weight could be quenched to a completely amorphous state.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 1270-1277 
    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 non-isothermal crystallization of Fortron poly(phenylene sulfide), PPS, was examined to better understand its behavior during injection molding. The nonisothermal Avrami formalism was applied to this system, but this method was found to be questionable because of the sometimes severe curvature that appears in the plots of the transformed data. A method of ranking crystallization rates at low cooling rates by plotting the peak in the crystallization exotherm versus the cube root of cooling rate has been considered and shown to have limitations at the higher cooling rates of interest. The growth rate expression developed by J. D. Hoffman for polymer crystallization of chain folded lamella in three dimensions has been used to simulate crystallization exotherms. It was found that this could only fit the data at low cooling rates. At high cooling rates it was necessary to use a growth rate expression developed by Calvert and Ulhmann for polymer crystallization without chain folding. When this is used to describe a two dimensional growth geometry, close agreement in the positions of high cooling rate exotherms could be obtained. The implication is that a change in crystallization mechanism is possible as the conditions go from low to high cooling rates.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1819-1831 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrocoating by polymerization of aqueous zinc chloride solutions of acrylamide and methylenebisacrylamide has been reexamined. The original investigators of this system proposed a mechanism in which the initiation was formed by electrochemical reduction of a zinc complex of molecular oxygen. That mechanism is not compatible with the present findings that polymerization occurs when oxygen is excluded by nitrogen bubbling. Evidence is presented for the intervention of a zinc complex with monomer. The pH dependence of electrocoating indicates that the species involved is ZnOH+. Failure to achieve coating in acidic solutions of monomers in the absence of zinc points to a multisite attchment of the metal species to monomer in a ring structure. The interpretation is consistent with the observed electropolymerization of N,N-dimethylacrylamide and with the correlation of electropolymerizability with shifts detected in laser Raman spectra of selected acrylic monomers.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 13 (1975), S. 73-78 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 17 (1979), S. 667-671 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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