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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 24 (1986), S. 65-67 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1919-1925 
    ISSN: 0887-6266
    Keywords: positron annihilation ; polymer electrolyte ; network polymer ; poly(glycidyl ether) ; polyether ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lifetimes of positrons have been measured for network polymers based on polyethers. From the temperature dependence of the lifetime of ortho-positronium (o-Ps), τ3, for the network polymer of poly(ethylene oxide-co-propylene oxide) [P(EO/PO)], an onset temperature for limited local motions of molecules, Tγ, and the glass transition temperature, Tg, were determined to be 57 and 201 K, respectively. For the network polymer of poly[EO-co-2-(2-methoxyethoxy)ethyl glycidyl ether] [P(EO/MEEGE)], Tγ and Tg were determined to be 57 and 185 K, respectively. For both specimens, above 270 K, the observed linear temperature dependence of τ3 was attributed to the thermal expansion of open spaces in a liquid state. In the temperature range between Tγ and 270 K, for the P(EO/MEEGE) network, τ3 was longer and its intensity was smaller than those for the P(EO/PO) network. These results were attributed to the increase in the size of open spaces for the P(EO/MEEGE) network polymer and the blocking of these regions by motions of side chains and chain ends. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1919-1925, 1998
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2721-2730 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of acrylonitrile (AN) with sodium p-styrenesulfonate (SSS) in dimethyl sulfoxide solution has been investigated. Monomer reactivity ratios at 45°C., for AN and SSS are found to be r1 = 0.15 ± 0.02, r2 = 0.55 ± 0.03. From these data Price Q and e values for SSS of 0.44 and -0.38, respectively, are calculated. The values are found to be different from those in aqueous solutions, which may be attributed to the different electron distributions in all solvents. Initial rates of copolymerization at 45°C. with azobisisobutyronitrile as initiator were determined over the entire range of composition from pure AN to pure SSS. It was found that there is a slight rise in copolymerization rates in the range of 90-95 mole-% SSS in the monomer feed; this is attributed to the coexistence of liquids of different optical density. Homopolymerization of AN and SSS in dimethyl sulfoxide was also investigated and δ = (kt½/kp) for AN and SSS found to be 6.55 (mole-sec./1.)½ and 2.46 (mole-sec./1.)½, respectively. From these values the cross-termination constant ϕ is calculated to be 6.5.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 18 (1980), S. 761-764 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 22 (1984), S. 659-663 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 23 (1985), S. 349-352 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 705-714 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of acrylonitrile (AN) with sodium p-styrenesulfonate (SSS) in aqueous solutions (of pH 3 and pH 7) has been investigated. Monomer reactivity ratios at 45°C. for AN and SSS are found to be r1 = 0.10 ± 0.02, r2 = 1.20 ± 0.10 at pH 3 and r1 = 0.05 ± 0.01, r2 = 1.40 ± 0.04 at pH 7, from which Price Q and e values for SSS of 0.76 and -0.26 at pH 3 and of 1.25 and -0.43 at pH 7 are calculated. Initial rates of copolymerization at 45°C. with ammonium persulfate (APS) as initiators were determined over the entire range of composition from pure AN to pure SSS, and it has been found that there is a sharp rise in copolymerization rates within 0.2-5 mole-% monomer feed, sometimes being eight times larger than those in the neighboring range. The copolymerization in SSS monomer feed of 0.2-5 mole-% occurs in the transition phase from homogeneous to heterogeneous, and the system is very viscous and slightly cloudy. From the investigation of the effect of initiator concentration on the copolymerization rate and the direct observation by an electron microscope, the sharp rise in copolymerization rates may reasonably be interpreted in terms of the emulsion copolymerization mechanism.
    Additional Material: 4 Ill.
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