Thermoplastics Modified with Nanoscale Inorganic Macromers
Abstract
We have taken a unique approach to the synthesis and study of hybrid organic/inorganic materials. Our method involves synthesizing nano-size inorganic P(l0)R(7)Si(8)O(12) clusters which contain seven inert "R" groups for solubility and only one functional "P" group for polymerization. This strategy permits the synthesis of melt processable, linear hybrid polymers containing pendent inorganic clusters and allows us to study the effect these clusters have on chain motions and polymer properties. The synthesis of norbornenyl-based polyhedral oligomeric silsesquioxane (POSS) macromers, their ring opening metathesis copolymerizations with varying amounts of norbornene, and analysis of the effect of the pendent POSS group is presented. The mechanical relaxation behavior and microstructure of norbornyl-POSS hybrid copolymers have been examined for their dependencies on the mole fraction of POSS-norborny monomer, as well as for potential sensitivity to the seven inert "R" groups present in each POSS macromer. POSS copolymerization is observed to enhance the cc-relaxation temperature, T(alpha) in proportion to the mole fraction of POSS-norbornyl comonomer. Interestingly, however, the magnitude of this dependence is larger for POSS-norbornyl comonomer possessing cyclohexyl groups (CyPOSS) than for cyclopentyl groups (CpPOSS). While POSS copolymerization yields only slight enhancement of the tensile storage modulus measured near room temperature at temperatures lower than a strong mechanical relaxation ((Beta)-relaxation near T = -75 degrees C), there is a significant POSS-reinforcement of the storage modulus.
Document Details
- Document Type
- Technical Report
- Publication Date
- May 26, 1998
- Accession Number
- ADA409391
Entities
People
- Amy R. Farris
- Angel Romo-uribe
- Hong G. Jeon
- Patrick T. Mather
- Timothy S. Haddad
Organizations
- Air Force Research Laboratory