Polychloroprene, also known as neoprene, is an elastomer commonly utilised
in the electrical and automobile industries. Its degradation is known to oc
cur predominantly in a two stage process: HCl is lost in the initial step,
whilst the second step involves the production of volatile hydrocarbons thr
ough chain scission. In this paper we describe the use of solid state C-13
NMR as a probe for structural changes in the condensed phase during these d
egradative steps. Cross polarisation-magic angle spinning (CP-MAS) analysis
of virgin polychloroprene and a series of samples degraded at temperatures
between 275 and 550 degreesC reveals that as degradation becomes more adva
nced there is a steady loss of sp(3) carbon with a commensurate growth in s
p(2) carbon. The bulk of the chlorine loss occurs by 350 degreesC with the
aliphatic carbon lost by 550 degreesC, by which temperature the residue is
essentially aromatic carbon. Dipolar dephasing experiments show that this r
esidue is essentially a network of, on average, tri-substituted phenyl ring
s. (C) 2001 Elsevier Science Ltd. All rights reserved.