期刊
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
卷 148, 期 2, 页码 229-241出版社
SPRINGER
DOI: 10.1007/s10973-022-11404-6
关键词
Styrenic polymer; Chemical modification; Thermal stability; Combustion characteristics; Phosphorus-nitrogen cooperative effect; Polystyrene
This study investigated the effects of covalently bound phosphorus (P-) and nitrogen (N-) bearing groups on the thermal and combustion attributes of polystyrene. The results showed that the presence of nominal amounts of P- and N- containing groups significantly altered the thermal stability and combustion characteristics of polystyrene, with enhanced char formation and reduced heat release rates and heat release capacities.
The effects of covalently bound phosphorus (P-) and nitrogen (N-) bearing groups on the thermal and combustion attributes of polystyrene have been investigated. The necessary chemical modifications were achieved through co- and ter-polymerisation reactions, in a suitable solvent, under radical initiation conditions. The influence of P-N cooperative interactions on the combustion properties of styrenic polymers was studied. The co-monomers of interest included: diethyl(acryloyloxymethyl)phosphonate (DEAMP), diethyl-p-vinylbenzylphosphonate (DEpVBP), acrylic acid-2-[(diethoxyphosphoryl)methyl amino]ethyl ester (ADEPMAE) and maleimide (MI). For the first time, the ter-polymers of styrene containing both P- groups, DEAMP or DEpVBP, and N- groups, MI, were prepared via solution polymerisation. It was found that the thermal stability and combustion characteristics of polystyrene were significantly altered by the presence of nominal amounts of P- and N- containing groups, and, in certain cases, cooperative interactions of these groups were also evident. For instance, the extents of char formation post-degradation of the prepared ter-polymers, as revealed by thermogravimetric investigations in an inert atmosphere (nitrogen), were found to be enhanced by more than 20%, as compared to the unmodified polystyrene. The heat release rates and heat release capacities of the ter-polymers, as measured using the pyrolysis combustion flow calorimetric (PCFC) technique, were reduced by almost 50% in comparison to the same parameters obtained for the unmodified counterpart.
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