Valbone Shabani , Wael Ali , Bassem Assfour , Raphael Otto , Dennis Killa , Seden Caglar , Ying Feng , Eui-young Shin , Jochen S. Gutmann , Thomas Mayer-Gall
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引用次数: 0
Abstract
Phosphorus and nitrogen-containing flame retardants are well-known for their high efficacy when used in combination, either as separate compounds or within the same molecule. However, a detailed examination of the chemical bonding of phosphorus is needed to understand the flame behavior. To this end, two different scenarios were examined and compared with a phosphorus-free benchmark. Both scenarios contain a triazine ring and a silane-based precursor. The first scenario involves a direct bond between phosphorus and triazine (phosphonate), while the second involves a bridging of phosphorus and triazine via nitrogen (phosphoramidate). This allowed to investigate the structural effect of phosphoramidate and phosphonate of triazine derivatives on the thermal and flame retardant behavior. The flame-retardant performance and mechanism of the treated samples were investigated by means of the vertical flame test (DIN EN ISO 15025), thermogravimetric analysis and microscale combustion calorimetry, amongst others. Our research shows that triazine-based phosphonate has a better flame retarding effect on cotton than phosphoramidate at the same phosphorus concentration. Self-extinguishing characteristics was observed at a low add-on value of 0.23 mmol/g for phosphonate-based flame retardant, while a higher add-one value of 0.24 mmol/g was required in the case of phosphoramidate. The comprehensive analysis demonstrated that both flame retardants undergo mechanisms in both the gas phase and condensed phase by releasing incombustible gases and promoting the carbonization of cotton fabrics.
期刊介绍：
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.
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