Thermoplastic Elastomers—Three Decades of Progress

Abstract

Abstract In these three decades of progress, thermoplastic elastomers have risen in 1987 to a position of tenth in the order of commercial thermoplastic sales in the U.S.A., with a growth rate, 1986–1987, of 9.7%. It is very probable that the quantity shown for 1987 sales, 441 million pounds, is low, since it is well known that the largest producer of styrenic TPEs does not report offtake data. Much of the styrenic TPE goes to the adhesive industry, which also is very secretive in regard to materials consumption information. Thus, the 1986–1987 reported growth rate of 9.7% is on the low side. Another indicator of progress in the growth of TPEs has been illustrated by the number of product introductions from January 1986 to June 1987. During that period, TPEs led the major thermoplastics with the introduction of 270 new product types, and the nylons were a close second with 250. A third estimate of the explosive growth in TPEs may be seen in Table V which lists the number of manufacturers of TPEs in 1975, 1985, and 1987, increasing from 10 to 28 to 50. To summarize, the present thermoplastic elastomers, now high-volume commercial products, had roots in the chemistry and technology of polymers in the 1920's. Throughout the history of the “Roots” period one can detect precursor events from which several TPEs could have been foreseen. In each of the three decades of progress, major advances were made in the technology, physical properties, availability, and utilization of TPEs. The numbers of these increased in each succeeding period. Several paradigms appear in this review, for example: 1. The triblock styrene-diene A-B-A copolymers, morphology, and elastomeric character, in the first decade. 2. The copolyesters with (A−B)n morphology and greatly enhanced physical properties in the second decade. 3. The dynamically-vulcanized blends of EPDM and PP, followed in time by the concept of compatibilization to permit practical blends of NBR and PP in the third decade. Throughout these periods, growth was catalyzed by the favorable economics of manufacturing finished elastomeric products via low-cost thermoplastic processing techniques as compared with thermoset rubber processes. The reuse of scrap also provided a major incentive. In addition to these, the concept of component integration is now showing a path toward even more cost reduction incentives. New applicational areas continue to appear. One of these, blending relatively small amounts of TPEs with existing large volume thermoplastics, promises to provide extremely large offtakes of TPEs in the next decade. I am sure that the numbers of papers presented in symposia at meetings of the Rubber Division of the American Chemical Society confirm the continued explosive growth of TPEs we have seen in these past three decades.