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6633497 
Journal Article 
Mechanistic modeling of polymer degradation: A comprehensive study of polystyrene 
Kruse, TM; Woo, OS; Wong, HW; Khan, SS; Broadbelt, LJ; , 
2002 
1 
Macromolecules
ISSN: 0024-9297
EISSN: 1520-5835 
AMER CHEMICAL SOC 
WASHINGTON 
7830-7844 
WOS:000178129900040 
The degradation of polystyrene was modeled at the mechanistic level by developing differential equations describing the evolution of the moments of structurally distinct polymer species. This work extends our previous modeling work(1) by incorporating chain-length-dependent rate parameters, tracking branched species more explicitly, using rate parameters primarily from the literature, and comparing the model results to extensive experimental data on the degradation of polymers of different molecular weights and at different temperatures. Unique polymer groups were devised that allowed the necessary polymeric features for capturing the degradation chemistry to be tracked, while maintaining a manageable model size. The conversion among the species was described using typical free radical reaction types, including hydrogen abstraction, midchain beta-scission, end-chain beta-scission, 1,5-hydrogen transfer, 1,3-hydrogen transfer, radical addition, bond fission, radical recombination, and disproportionation. The model included over 2700 reactions and tracked 64 species. Programs were developed using the programming language Perl to assemble moment equations from input of the polymeric features to be tracked. The intrinsic kinetic parameters (a frequency factor and activation energy for each reaction) were obtained from data in the literature and previous modeling work in our laboratory.(2-4) The model predictions for the evolution of M-n and M-w and the yields of styrene, dimer, and trimer compare very well with experimental data obtained in our laboratory for the degradation of polystyrene over a large temperature range and with different initial molecular weights. Evolution of low molecular weight products from experiments reported in the literature is also captured.