62 Fundamentals of Bis-Maleimide Cure Chemistry

Wednesday, October 12, 2011: 2:30 PM
Meeting Room #16 (The I-X Center)
Karthik Vikram Siva Shanmugam1, J. Scott Parent, Dr.1 and Ralph A. Whitney2, (1)Department of Chemical Engineering, Queen's University, Kingston, ON, Canada, (2)Department of Chemistry, Queen's University, Kingston, ON, Canada
Radical-mediated polymer modifications are robust and inexpensive methods of transforming commodity elastomers and thermoplastics into thermoset articles. Although coagent technologies for improving cross-linking yields are well-established, commercial development has evolved faster than our understanding of underlying chemical principles. This report aims to develop an understanding of a bis-maleimide based coagent system.

 Rheological studies of cis-polybutadiene and LLDPE cure dynamics and yields are augmented with model compound studies to build a mechanistic understanding of these systems. NMR and MS analysis of the products derived from reacting N-phenylmaleimide with cyclooctane indicates that C-H bond addition is the primary means of cross-linking in LLDPE. Similar studies of N-phenylmaleimide reactions with cis-cyclooctene revealed an alternating copolymerization mechanism for polybutadiene + bis-maleimide cures.