Euide~,:e is #neunted that burning polyme[hyI metkaerylate and po~yoaymethylene do no~ react ch,miΒ’ally rvitlt the gas around them, but merely vapome it, the hoar o! the surrouncIi~g diflusiott [lames, The pyrolysis products oxidize subsequenffy in the flames. Polyethylene probab.fy bu~ similarly, b
Flammability of polymers
β Scribed by C.P. Fenimore; F.J. Martin
- Book ID
- 103040122
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- English
- Weight
- 409 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0010-2180
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β¦ Synopsis
The/tammability of polymers has been measured by determining the oxyge~ content of the, atmospheres just capalde o/ burning them. The effects of the ]ollowing three commonly used al,,ents for reducing l~ammability have been compared in polyethylene. (I) A moderate degre,~ o] inhibition is con/erred by antimony trioxide plus su~cient chlorine: the maximum effect requires about 0.01 antimony atoms per Ce group in the polyethylene, and develops just as well when chlorine~antimony is six as Β’~hen it is twenty. The lull effect o] the antimony does not develop when chlorine~antimony is two. ( 2) Various phosphorus compounds are all o/ similar effectiveness per atom o] phosphorus added to polyethyh;ne. ( 3) With su~cient substitution o/ hydrogen by hatogen in polyethylene, a greater inhibition is achieved than ~s possible by (t) or ( 2). We have no evidence how, ( 1) and ( 2) inhibit burning, bat present evidence is that in (3) a large substitution of chlorine works mostly by affecting the degradation of the polymer rather than by inter/ering with gas phase flame reactions.
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