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Polymer and
Biomaterial applications
The effects of ultrasound on
polymers (giant molecules formed by the coupling of small
molecules-monomers) have been thoroughly studied over the past 30 years. The
controlled cleavage of polymers in solutions irradiated with ultrasound has
been examined in detail. Polymer degradation produces chains of smaller
lengths with relatively uniform molecular weight distributions, with
cleavage occurring primarily in the center of the polymer chain. Several
mechanisms have been proposed for this sonochemical cleavage, which is
usually described as a mechanical breakage of the chains induced by shock
waves or solvent flow created by cavitation during the ultrasonic
irradiation of liquids.
This polymer fragmentation has been
used by G. J. Price at the University of Bath to synthesize block copolymers
of various sorts. Block copolymers are long chain polymers with two
different, but linked, parts. As an analogy, imagine a train made up in
front by passenger cars and in back by freight cars. In this fashion, block
copolymers can do double-duty in their properties. Peter Kruus at Carleton
University, Ottawa, reported the use of ultrasound to initiate
polymerization in solutions of various monomers.
Applications of ultrasound to the
synthesis of biomaterials are under rapid development. While the chemical
effects of ultrasound on aqueous solutions have been studied for many years,
the development of aqueous sonochemistry for biomaterials synthesis is very
recent. The area of protein microencapsulation has proved especially
interesting. Microencapsulation, the enclosing of materials in capsules a
few micrometers in size, has diverse important applications; these include
uses with dyes, flavors and fragrances, as drug delivery systems, and as
medical diagnostic agents.
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