## Abstract Poly(amide imide)βepoxysilane (coupling agent) composites were reacted with silica, a condensation product of tetraethylorthosilicate (TEOS), by a solβgel process and were then cast into films. After this procedure, the chemical characteristics and mechanical and thermal properties were
Thermal decomposition of amide and imide derivatives of maleated polyethylene
β Scribed by Liyan Huang; Yi Shi; Liusheng Chen; Xigao Jin; Ronghua Liu; Mitchell A. Winnik; David Mitchell
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 215 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
The thermal decomposition behavior of six derivatives of maleated polyethylene was investigated by high-resolution pyrolysis gas chromatography-mass spectrometry. The results revealed that substituents attached to maleated polyethylene as amides formed from secondary amines were significantly less stable than imides formed from primary amines. Morpholine amide and N-methylaniline amide derivatives of maleated polyethylene underwent significant decomposition at 160 Β°C and substantial decomposition at 200 Β°C. In contrast, the imide derivatives of maleated polyethylene were stable for long periods of time at elevated temperatures. Following 2 min of heating, the first traces of decomposition were detected at 200 Β°C for the 2-aminoanthrancene imide derivative, at 255 Β°C for the 2-phenethylamine imide, and at 280 Β°C for the 9-aminomethylphenanthrene imide. With the exception of the 9-aminomethylphenanthrene imide, all other derivatives decomposed to form the corresponding amine as the single most significant volatile product. The most likely explanation for this result is that the polymer contained small amounts of succinamic acid that did not close to form the imide. We concluded that the imide was stable even to 315 Β°C and that the amine was lost from β€-carboxyamide groups present in the sample. In the 9-aminomethylphenanthrene imide derivative, we observed no loss of amine. Instead, we observed an alternative fragmentation process yielding 9-methyl phenanthrene. The dependence of the thermal stability of these various derivatives of maleated polyethylene has important implications for the design of reactive-blending strategies for polyolefins with other functional polymers.
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Pyrolysis-GC/mass spectrometry experiments reveal that naphthalene groups attached to maleated polyethylene as the 1-naphthylethyl ester are stable for relatively long periods of time a t 170Β°C. Decomposition can be detected for samples heated for 2.0 min a t 2OO0C, but even a t t h a t temperature,
## Abstract Thermal decomposition of imipramine hydrochloride and trimipramine maleate has been investigated isothermally and nonisothermally. The kinetic parameters, namely the activation energy __E__~a~ and the Arrhenius preexponential term __A__, were calculated. Applying the theory of activated
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