Effect of comonomers on thermal degradation of polyacrylonitrile
β Scribed by D. C. Gupta; J. P. Agrawal; R. C. Sharma
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 340 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
The thermal degradation of polyacrylonitrile and copolymers of acrylonitrile (AN) with each of vinylacetate (VAC), methallyl sulfonate sodium salt (MASS), and 2-acrylamido 2-methyl propane sulfonate sodium salt (2-AMPSS) i.e., P(AN-VAC), P(AN-MASS), P(AN-AMPSS), and P(AN-VAC-MASS), has been investigated using the technique of thermogravimetry and differential scanning calorimetry (DSC). The initial decomposition temperature (IDT) and integral procedural decomposition temperature (IPDT) for all the copolymers are less than that for polyacrylonitrile irrespective of the nature of the vinyl comonomers. TGA thermograms indicate faster rate of degradation in copolymers compared to polyacrylonitrile. Variation in the glass transition temperature is correlated to the polarity of the functional groups in the polyacrylonitrile copolymers.
π SIMILAR VOLUMES
PAN undergoes chemical decomposition in stages on thermal treatment. In the literature, several mechanisms were proposed for the degradation process. However, the decomposition pathway and the structural rearrangement of solid residue in relation to the loss of volatile products are not fully unders
## Abstract The effect of incorporating phthalate, 1,8βnaphthalenedicarboxylate, and 1,8βanthracenedicarboxylate structural units on the crystallization rate of PET are evaluated by isothermal and dynamic calorimetry. Although all of the comonomers retard crystallization, the 1,8βnaphthalene unit s