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nitrocellulose from the mass loss and extends into the temperature interval of transformation of char residue, DSC covers relatively narrow temperature interval of the exothermic process occurring very fast in an explosion like manner. The disadvantage of DSC
Abstract
The effects of some kinds of metal ions used as chemical modifications on the thermal properties of the modified polyacrylonitrile (PAN) fibers were studied by DTA, TG, GC and cone calorimetry. The apparent activation energies for the decomposition of the unmodified and modified PAN fibers were determined using Kissinger equation and Broido equation.
decomposition of hemicellulose and cellulose into char residues and the production of CO 2 , CO, CH 4 , CH 3 OH, and CH 3 COOH. During this stage, the mass loss on the TG curve accelerates gradually as the temperature is increased [ 16 – 18 ]. The calcining
the organic group containing phosphorus. Specifically, the acid environment from the degradation products accelerated the dehydration of cotton fabrics. At the same time, with the addition of DIA, char residues increased from 1.82 to 9.38 wt% at 700 °C
Abstract
Thermogravimetry-mass spectrometry (TG-MS) was used to study the effect of the inorganic salts (NH4)2SO4 and (NH4)2HPO4, active substances of many commercial forest fire retardants, on the pyrolysis of Pinus halepensis needles and their main components (cellulose, lignin and extractives). These salts seemed to affect the pyrolysis of cellulose by increasing significantly the char residue, decreasing the pyrolysis temperature and changing the composition of the evolved gases, that is, increasing levoglucosenone and decreasing oxygen containing volatile products. (NH4)2SO4 seemed to have negligible effect on the pyrolysis of lignin, while (NH4)2HPO4 increased the char residue and decrease the relative contribution of guaiacols in the evolved gases. No effects of the inorganic salts on the extractives were observed. Finally, the inorganic salts seemed to affect the pyrolysis of pine-needles, mainly the cellulose component, but the effects were not as intense as in the pyrolysis of cellulose.
Abstract
The thermal degradation behavior of P. halepensis needles treated with two ammonium-polyphosphate-based commercial retardants was studied using thermal analysis (DTG) under nitrogen atmosphere. Moreover, for the same experimental material, the heat of combustion of the volatiles was estimated based on the difference between the heat of combustion of the fuel and the heat contribution of the charred residue left after pyrolysis. The heat of combustion of the volatiles was exponentially related to the retardant concentration of the samples. In the range of retardant concentrations from 10 to 20% w/w the mean reduction percentage of the heat of combustion of the volatiles, with respect to untreated samples, was 18%.
Abstract
The synergistic effects of zinc oxide (ZnO) with layered double hydroxides (LDH) in ethylene vinyl acetate copolymer/LDH (EVA/LDH) composites have been studied using thermal analysis (TG), limiting oxygen index (LOI), UL-94 tests, and cone calorimeter test (CCT). The results from the UL-94 tests show that the ZnO can also act as flame retardant synergistic agents in the EVA/LDH composites. The CCT data indicated that the addition of ZnO in EVA/LDH system can greatly reduce the heat release rate. The TG data show that the ZnO can increase the thermal degradation temperature and the charred residues after burning.
Abstract
Structurally different poly(arylene ether sulphone) (PES) copolymers were synthesized by reacting stoichiometric amount of dichlorodiphenyl sulphone (DCDPS) with bisphenols. The molar ratio of bisphenol-A and phenolphthalein (ESP)/hydroquinone (ESH)/resorcinol (ESR) was varied to prepare nine copolymer samples. Structural characterization was done by FT-IR and 1H-NMR studies. The initial decomposition temperature as well as temperature of maximum rate of mass loss in ESR and ESH copolymers were similar and a marginal decrease in these decomposition temperatures were observed by increasing the isopropylidine units in the backbone. High char residue at 800C was observed in polymers having high content of phthalein units.
Abstract
Curing of diglycidyl ether of bisphenol-A (DGEBA) with phosphorus containing amide amines i.e. bis[3(3’-aminobenzamido phenyl)]methyl phosphine oxide (MB),bis[3(4’-aminobenzamido phenyl)]methyl phosphine oxide (PB), tris[3(3’-aminobenzamidophenyl)] phosphine oxide (MT) and tris[3(4’-aminobenzamido phenyl)] phosphine oxide (PT)and conventionally used curing agent 4,4’-diaminodiphenyl sulfone (D) was studied by DSC. The amines MB, PB, MT and PT were synthesised in the laboratory and were characterized by determining elemental composition, melting point, and amine equivalent. Structural characterization was done by 1H-NMR and FTIR. The onset temperature of curing depended on the nucleophilicity of the amines and was in the orderMT≈MB<PT<PB<D. The exothermic peak temperatures were in the orderD>PB>PT>MT≈MB. The char residue of cured epoxy resin was significantly higher when phosphorus was incorporated in the cured network. Using mixed amine formulations based on amine D and P-containing amines and the molar ratio of these amines could easily control the curing characteristics. A linear relationship between char yield and P-content was observed in such formulations.
level of flame retardancy. The effects of flame retardants on the main gaseous products of the thermal decomposition were analyzed by the thermogravimetry–mass spectrometry analysis, and the morphology of the char residue was also observed by a scanning
