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:
ABA-type block polymers of styrene (monomer A) and isoprene or butadiene were prepared using two commercially available dilithium adducts of isoprene as initiators. One (DiLi-1) was predominantly dilithio diisoprene and contained a small amount of dimethyl ether (ether/Li 〉 1.0). The second (DiLi-1 C.E.) was a higher molecular weight version of DiLi-1, containing about seven isoprene units per molecule. It contained only a trace of dimethyl ether (ether/Li 〈 0.1). Polymers were made by charging all of the monomers at the start of the reaction. The diene polymerized first, incorporating some styrene. When the diene was consumed, the difunctional polymer chains then added a block of nearly pure polystyrene at each end. Thus an ABA-type polymer was synthesized in one step. These polymers show the usual behavior of pseudo-vulcanized elastomers. Their stress-strain curves are given. The SBS polymers had the higher tensile strengths. None had tensile strengths as high as SBS or SIS polymers made with n- or sec-butyllithium. It was shown that the diene blocks contain appreciable amounts of styrene. This leads to more compatibility between the A and B blocks; it also shortens the styrene blocks compared to the theoretical lengths of “pure” blocks. Both effects can lead to loss of tensile strength. Microstructures of the diene homopolymers made with these initiators are also given.
Additional Material:
6 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/app.1972.070160115
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