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  • 1
    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: A study has been carried out on the preparation of block copolymers of styrene-dimethylsiloxane and isoprene-dimethylsiloxane. This has been accomplished by means of anionic polymerization, using potassium metal or potassium naphthalene as initiator, in tetrahydrofuran. Block copolymers of the ABA type were synthesized by first preparing the polystyrene or polyisoprene dianion, followed by polymerization of the octamethylcyclotetrasiloxane. Proof of the presence of these block copolymers was obtained from their solubility behavior and from the ability of the isoprene-siloxane polymers to undergo vulcanization by sulfur. The chain length of the polymeric blocks could be controlled in a predictable fashion, leading to a central segment (B) of polystyrene or polyisoprene, having a narrow molecular weight distribution, and two end segments (A) of polydimethylsiloxane, having a most probable distribution. The reverse type of block copolymer was not possible due to the inability of the siloxane to initiate styrene or isoprene polymerization.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study has been carried out on the molecular weights and their distribution for polystyrene prepared by means of ethyl and butyl lithium initiators, using benzene and tetrahydrofuran as solvents. Stringent high vacuum techniques were employed in order to minimize any destruction of initiator or termination of growing chains in these anionic polymerizations. Under these conditions, it was found that the stoichiometry corresponded to the formation of one chain from each initiator molecule. Furthermore, the molecular weight distribution could be made very narrow (M̄w/M̄n = 1.05 - 1.1) in these cases, where the initiation reaction was very rapid compared to the propagation step. In the case of the benzene systems, the initiation reaction was too slow, leading to a broadening of the molecular weight distribution, and this could be circumvented by a “seeding” technique whereby all the chain anions were pre-initiated before the main polymerization took place. The alkyl lithium initiators were found to react rapidly with THF at room temperature, but the styryl lithium apparently did not.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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