Samples of Nylon G/poly(propylene oxide), with poly(propy1ene oxide) (PPO) content varying up to 35%, have been examined using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and nuclear magnetic resonance (NMR) carbon-13 at solidstate. Carbon-13 spectra were measured by c
Carbon-13 NMR high-resolution study at solid of polyamide 6/PPO blends containing compatibilizer-block copolymer and polycarbonate
✍ Scribed by Dilma Alves Costa; Edemilson P. Silva; Clara Marize F. Oliveira; Maria Inês B. Tavares
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 146 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Two types of blends containing polyamide 6 and poly(propylene oxide) (PPO) were prepared. One of them was mixed with polycarbonate (PC) in a Brabender mixer. The other one was prepared in solution with the block copolymer as the interfacial agent. The blends were analyzed by 13 C nuclear magnetic resonance techniques at solid state, such as: magic angle spinning (MAS); cross-polarization MAS, and variable contact time experiment. It was observed that the addition of PC in the nylon 6/PPO system causes a hardening of it, which can be attributed to strong links, like a hydrogen bond. The ideal quantity of block copolymer added to a blend to improve the compatibility is between 5 and 10%. An increase of the quantity of this agent probably makes it act as a third component. Therefore, both PC and block copolymer can be used as an interfacial agent for nylon 6/PPO blends in an ideal composition.
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