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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 253-259 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polybutadiene of high molecular weight was prepared in hydrocarbon solvent by using n-BuNa-tert-BuOM (M = Li, K) as a polymerization initiator. The microstructure of this polymer varied from 35 to 76% of 1,2 content, depending on the type of modifiers. The kinetics of polymerization was not studied, primarily due to the heterogeneous nature of the catalyst. However, other variables, such as the catalyst concentration and temperature, have been studied. The results and mechanistic implications are discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2401-2410 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An organolithium reagent substituted with a primary amine-protecting group [i.e.,—N(TMS)2] has been prepared and used to polymerize 1,3-butadiene and isoprene. A method is described for converting the resulting—N(TMS)2-containing polydienes into—NH2-containing polymers. Both —N(TMS)2- and —NH2-terminated polydienes have been characterized with regard to microstructure, Mn, and Mw/Mn data, as well as qualitative and quantitative end-group analyses. The described preparative procedures represent a convenient route to the elusive primary amine-terminated polydienes.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1847-1848 
    ISSN: 0360-6376
    Keywords: Physics ; 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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  • 4
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organolithium reagents substituted with hydroxyl-carrying mixed acetals (i.e., tetra-hydropyranyl and α-ethoxyethyl ethers) have been prepared in high yields and used to polymerize 1,3-butadiene to various acetal-terminated polybutadiene polymers. A method is described for converting acetal-containing polymers into hydroxyl-containing polymers. The polybutadienes have been characterized with regard to endgroup types, quantitative functionalities, molecular weights, molecular weight distributions, and microstructures. Dihydroxyl terminated polymers are prepared anionically in the absence of gel. Such materials are more suitable from the standpoint of f(OH) and M̄w/M̄n for chain extension studies than are prepolymers prepared by radical methods.
    Additional Material: 3 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 14 (1976), S. 497-506 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polybutadiene was successfully metalated by use of tert-butyllithium activated with alkoxides of Group I metals without chain degradation. The metalated polymer was grafted with styrene and 1,3-butadiene to give novel graft copolymers of varying microstructure. This metalating system was found to be highly efficient; however, its catalyst effectiveness is less than that of organolithium-TMEDA metalation agent.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0959-8103
    Keywords: anionic copolymerization ; modelling studies ; styrene ; butadiene ; polymerization ; 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: The anionic polymerization of isoprene with n-butyl lithium and polar modifier such as TMEDA and tripiperdinophosphine oxide were studied and kinetic and reactor models are proposed for these systems. Reactor conversion, molecular weight distribution and polymer glass transition temperature had been calculated from the model and compared favorably to the actual data for various combinations of reactor systems and operating conditions. Simulations of the model can be used to design reactor systems and predict polymer properties of large-scale operations from results of small scale batch reactor runs.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 183-190 
    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: The average molecular interchain spacing (〈R〉) in Angstroms for amorphous polymers was calculated from the strong maximum in the wide-angle X-ray scattering (WAXS) diffraction scan using established equations. The half-width (HW) of the maximum was used to qualitatively describe the distribution of 〈R〉. 〈R〉 and HW for immiscible blends corresponded to the weighted average of 〈R〉 and HW of the homopolymers in the blend. 〈R〉 for a miscible blend (natural rubber and high-vinyl PBd) was much larger than the weighted average of 〈R〉 of the component homopolymers, indicating that a new amorphous molecular structure had developed. The larger 〈R〉 for the miscible blend indicates that the molecular chains are spread further apart, resulting in an increase in free volume to accommodate the new packing order. The single Tg of this blend was lower than predicated by the Gordon-Taylor equation.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1589-1599 
    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: The anionic solution polymerization of isoprene with n-butyllithium (n-BuLi) initiator and tetramethylethylenediame (TMEDA) modifier or n-butyllithium (n-BuLi)initiator and tripiperidinophosphine (TPPO) modifier was studied and kinetic and reactor models are proposed for both systems. Reactor conversion, molecular weight distribution, and polymer glass transition temperature had been calculated from the model and compared favorably to actual data for various combinations of reactor system and operating conditions. Simulations of the models can be used to design reactor systems, and predict polymer properties of a large-scale operation from results of small-scale batch reactor runs. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 861-871 
    ISSN: 0887-6266
    Keywords: glass transition ; polymer blends ; free volume ; positron annihilation ; composition dependence of Tg ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: High-Vinyl Polybutadiene (HVBD)/cis-Polyisoprene (CPI) blends were characterized by Differential Scanning Calorimetry (DSC) and Positron Annihilation Lifetime Spectroscopy (PALS). A single DSC glass transition temperature Tg is observed, whose composition dependence strongly deviates from additivity, and shows an apparent cusp when the weight fraction of HVBD ≈ 0.75. The free-volume hole size, Vh, and the scaled fractional free volume, hps/C, = I3Vh were determined by PALS from the orthopositronium (o-Ps) intensities, I3, and lifetimes, τ3, over a temperature range encompassing Tg and the temperature at which “positronium bubble” formation occurs. In the glass, Vh and hps/C are smaller for CPI than for HVBD, but the thermal expansion coefficient for hole volume, αf, is larger in the melt for CPI than for HVBD; thus, an iso-hole volume temperature occurs in these blends at Tiso ≈ -34°C. Above and below Tiso, Vh and hps/C each show a negative departure from additivity. A quantitative interpretation of the cusp in the composition dependence of Tg can be obtained, via a modified analysis of Kovacs, using free-volume quantities from PALS, with the ratio of scaling constants CCPI/CHVBD as an adjustable parameter. At high temperatures, the positron bubble size is smaller in CPI than in HVBD. This agrees with the observation that the thermal expansivity of hole volume, and, hence the internal pressure are larger in the equilibrium melt of CPI. The effect of e+-irradiation on the o-Ps intensity was investigated. I3 decreases more rapidly in the melt as T → Tg, and then more slowly in the glass, suggesting that the effect is due to trapping of radical or ionic species which inhibit o-Ps formation. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 861-871, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 1319-1334 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of polar modifiers to alkyllithium-initiated homopolymerizations of butadiene causes substantial changes in the microstructure of the polymers produced. These changes are shown to depend not only on the concentration of modifier, but also on the polymerization temperature. The combined effects of modifier concentration and reaction temperature have been considered, and a method is presented for quickly determining the proper conditions for preparation of a polybutadiene of any 1,2-microstructure within a range of 10-80%. It is also shown that in anionic polar-modified copolymerizations of butadiene-styrene, the reaction temperature is again critical. Within a certain concentration range of modifier, the temperature will influence the rate of styrene incorporation or the randomness of styrene units in the resulting copolymers.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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